The COVID-19 “Bad Tryp” Syndrome: NAD/NADH+, Tryptophan Phenylalanine Metabolism and Thermogenesis like Hecatomb – The Hypothesis of Pathophysiology Based on a Compared COVID-19 and Yellow Fever Inflammatory Skeleton Tryptophan anti-inflammatory pathway and phenylalanine pathway Serotonin and the magnitude of the disease: Glucose resistance - neutrophilia and hyperthermia versus neutropenia and hypothermia

Introduction: There is a significant imbalance in the generation of NAD/NADH+ (niacin), which affects chemical reactions in the intracellular environment in COVID-19 and yellow fever. From tryptophan and its metabolic pathways and oxidative stress, the process of understanding SARS-CoV-2 infection becomes more concrete, as the infection seems to interfere in these metabolic pathways, in addition to the paradoxical role of kynurenine that causes inflammation by blocking the BH4 pathway. Understanding metabolic changes in the elderly, people with type 2 diabetes (DM2), obese people or other chronic diseases with an inflammatory profile of COVID-19 may immune Cathepsins of some amino acids the immune suppression metabolic syndrome (MS). Results: From overweight people to people with higher Body Mass Index (BMI) or insulin resistance, there is a tendency to hyperthermia by thermogenesis due to the consumption of serotonin (5-HT) and norepinephrine (NOR) in fat cells, an increased inflammatory state and cell damage. It with COVID-19 who been with antipyretic and antimicrobial at elevated temperatures, but the correct is an insulin pump. It is not fever; it is hyperthermia. The state of inflammation is related to the Kynurenine/BH4 imbalance. Objectives: This article aims to raise doubts to generate more discussions and bring more substrates to improve the patient's COVID-19. The primary pathophysiology of COVID-1 may be tryptophan syndrome due to kynurenine/ BH4 imbalance and the maintenance of the hypoxic environment that causes immunosuppression, tolerance and inflammation due to oxidative stress. A signature of innate immunity, oxidative stress, and tryptophan pathway imbalance. cells macrophages. Monocyte distribution, based on CD14+ CD16+ does not have significant change in the number of classic monocytes (CD14 ++ 16-ve), but an increase in intermediate (CD14++ 16+) and non-classic (CD14+ CD16++) subsets in patients compared to healthy controls. Shown classical double expression of positivity for HLA-DR/CCR2 and HLA-DR/CX3CR1 in patients with COVID-19; however, CCR2 expression was reduced in the intermediate subset in patients with COVID-19. Monocytes are heterogeneous and are classified into different subsets defined by the extent of their cell surface expression of CD14 and CD16. The main subset, termed classical monocytes, consists of CD14highCD16negative monocytes (CD14++ CD16−), while monocytes expressing CD16 are generally divided into an intermediate CD14highCD16low (CD14++ CD16+) subset and a CD14lowCD16high (CD14+ CD16+) subset not classic subset. Differential expression of the chemokine receptors CCR2 and CX3CR1 is associated with these human monocyte subsets with the classic CD14 ++ CD16− subset predominantly expressing CCR2 and the nonclassical CD14 + CD16 ++ subset showing lower CCR2 expression and significantly higher expression of CX3CR1. CCR2 and CX3CR1 are two chemokine receptors that regulate the responses of myeloid cells, such as monocytes and microglia, during inflammation. CCR2 and its ligand are crucial for the the the leading to their exit into cells of the M2 repair The of CX3CR1 and nonclassical monocyte subsets a more phagocytic phenotype greater an the of A shows that SARS-CoV-2, which we detected significantly higher expressions of MPO (~4 fold, p < 0.05) at the nasopharynx region, and speculates this neutrophil burst and even more overexpressed MPO may cause the production of excess hypochlorous acid (HOCl) and other reactive oxidants that also damage the nasopharynx MPO be important can become in


Introduction Praeludium a
As a ripening of the first [1] article we published, this new manuscript intends to explain, in a more organized a A prelude is a piece of music that precedes "something else", a fugue, for instance, or it could be the opening or the introduction of a suite. It normally has the function of preparing the listeners' ears for a certain affect through the composer's choice of key and time signature. and brain after being stimulated. Inflammation (mediated by infection or not) and hepatic hypoxia shift the Try metabolism to be carried out by the enzyme IDO, as these conditions decrease the expression of TDO in the liver and increase the expression of IDO in macrophages and dendritic cells (DCs), connective tissue (fibroblast) and epithelial tissue (pulmonary, renal, gastrointestinal and vascular), mainly stimulated by interferon-gamma (IFN-γ) and other lipid mediators such as prostaglandin E2 (PGE2) and pathogen particles such as lipopolysaccharide (LPS). IDO-1 is the predominant of the two enzymes and is found in many cell types including, but not limited to, astrocytes, neurons, microglia, dendritic cells, monocytes, and macrophage, whereas IDO-2 has only been found in a smaller subset of cells, primarily dendritic and stem cells and some cancer lines. IDO-1/IDO-2 is the enzyme responsible for catalysing the rate-limiting step in the peripheral tissues and depends on the active form of superoxide (O 2 -) [9-12] (Figure 1 and Figure 2).

The Kynurenine pathway
The Kynurenine pathway ( Figure 2) is initiated by conversion of l-tryptophan, by either of the enzymes tryptophan-2,3-dioxygenase or indoleamine 2,3-dioxygenase each forming formyl-kynurenine, which is then further degraded to kynurenine, the precursor of several bioactive compounds, including kynurenic acid, quinolinic acid, picolinic acid, and 3-hydroxyanthranilic acid. The pathway is responsible for over 90% of tryptophan metabolism in the periphery.
Kynureninase is a pyridoxal phosphate-dependent enzyme inhibited by oestrogen and metabolites, with both vitamin B6 deficiency and inhibition. There is an increase in Kyn, HK, XA, and HaA and a decrease in KA and AA because of the simulation of a general vitamin B-6 deficiency in which the activities of the enzymes were not completely reduced [8,13].
Naive CD4+T cells can differentiate into T helper (Th) cells, Th1, Th2, and Th17 lineages and regulatory T (Treg or CD3+CD4+FOXP3+) cells. -6 and transforming growth factor β (TGFβ) is considered critical for the differentiation into Th17 cells. IL-21 and IL-23 pathways are involved in IL-6-programmed Th-17 cell differentiation. Various cytokines regulate th17 differentiation. TGF-β and IL-6 induced th17 differentiation in mice, and IL-1β but not TGF-β has been shown to participate in the development of Th17 cells together with IL-6 in humans.
The development of Th17 cells is negatively regulated by IFN-γ, IL-27, and IL-2, the signals of which are dependent on Stat1 (IFN-γ and IL-27) and Stat5 (IL-2), respectively. The orphan nuclear receptors, retinoid-related orphan receptor γ (RORγ) and RORα have been identified as the key transcription factors that determine the differentiation of Th17 lineage. AhR is involved in the differentiation of Th17 cells by regulating Stat1 activation, which suppresses Th17 cell differentiation under Th17-polarizing conditions ( Figure 1 and Figure 2).

The kynurenine metabolic pathway is responsible for inflammatory control in an acute or chronic inflammation
IL-27 and IFN-γ suppressed the generation of Th17 cells without significant effects on the expression of RORγ. Th17 differentiation is positively regulated by IL-6 or IL-21 in combination with TGF-β and negatively regulated by IFN-γ or IL -27, which Stat3 and Stat1, respectively control. When the TGF-β1 signalling pathway is activated, the expression of RORγt and Foxp3 is upregulated. Whether naïve T cells polarize to a Th17 phenotype, or a regulatory phenotype largely depends on the surrounding microenvironments. Foxp3 can inhibit Th17 development by directly binding to RORγt. Without IL-6, the TGF-β signalling pathway reinforces this inhibition and favours the formation of Treg from naïve T cells. In the presence of IL-6, STAT3 can be activated, and Foxp3 is released from RORγt. During differentiation of Th17, the expression of IL-23R is also upregulated, and activated IL-23R can induce Th17 differentiation. IL-23R is also very important for the proliferation and maintenance of the phenotype of Th17 cells after differentiation. The IL-23 signalling pathway can also activate STAT3 and inhibit IL-10 production. TGF-β1induced Th17 differentiation can occur without IL-6 if there is sufficient IL-21 [14][15][16][17][18][19][20] (Figure 3).
Aryl hydrocarbon receptor (AhR) is a member of the basic helix-loop-helix-(bHLH) superfamily of transcription factors associated with cellular responses to environmental stimuli, such as xenobiotics and oxygen levels.
AHR is expressed in the innate immune system cells, such as dendritic cells, macrophages, natural killer cells, and lymphoid tissue inducer-like cells. In contrast to other danger-sensing systems, such as the TLR pathways, AHR signals are thought to convey intrinsic metabolic or oxidative stress in a cell type-specific manner. Engagement of AHR with different ligands modulates the expression of surface molecules of dendritic cells and the secretion of cytokines with either proinflammatory or tolerogenic net effects [21,22].
Aryl hydrocarbon receptor (AhR) is a member of the basic helix-loop-helix-(bHLH) superfamily of transcription factors associated with cellular responses to environmental stimuli, such as xenobiotics and oxygen levels. AHR is expressed in the innate immune system cells, such as dendritic cells, macrophages, natural killer cells, and lymphoid tissue inducer-like cells. In contrast to other danger-sensing systems, such as the TLR pathways, AHR signals are thought to convey intrinsic metabolic or oxidative stress in a cell-type-specific manner. Engagement of AHR with different ligands modulates the expression of surface molecules of dendritic cells and the secretion of cytokines with either proinflammatory or tolerogenic effects.
The cytokine profile in elderly patients has an immune signature associated with the disease with elevated CXCL8, IL-10, IL-15, IL-27, and TNF-α positively correlates with older age, more extended hospitalization, and a more severe form of the disease and may thus represent the leading signature in critical COVID-19 patients [23].
In the remaining patients, those with the severity of plasma concentrations of IFN-α, IP-10, MIG, IL-6, IL-8, MCP-1, IFN-γ, VEGF, and IL-10 were found to be significantly higher in the severe and critical group than those in other groups. The plasma concentrations of IFN-α, IFN-γ, IP-10, MIG, and IL-6 were elevated in the severe and critical group at 5-10 days from symptom onset. Although the plasma concentrations of VEGF and IP-10 gradually decreased with time, their levels were significantly higher in the severe and critical groups throughout hospitalization.
In severe patients under the age of 60 do not show significant leukocyte alterations and express high IL-1RA, IL-6, CCL2, CXCL1, CXCL9, CXCL10, and EGF. In contrast, older patients express high CXCL8, IL-10, IL-15, IL-27, and TNF-α, presenting a significant reduction in the total T lymphocyte number and an increased expression of T cell exhaustion markers as compared to the younger [16,[24][25][26][27].
Another study evaluated the cytokine profile in COVID-19 patients under oxidative stress, finding IL-6, IL-8, IL-10, VEGF, MCP-1 and EGF. This profile is compatible with critically ill patients, elderly or not, but with severity predictors such as T2DM, obesity, and insulin resistance [28].
In cases of Try starvation with critical shortage in tryptophan supply, the control of an immune response by IDO involves adjustable and versatile effects, including CD3ζ down-regulation and Treg generation by tryptophan deficiency and kynurenine production. CD4 + CD25 + Treg phenotype through a process requiring GCN2 and leading to a gradual decrease in IL-2 production and up-regulation of IL-10 and TGF-β [8,29].

Serotoninergic and oxidative signatures
In agreement with what has been explained so far, it appears that the inflammatory storm in COVID-19 has an innate immunity profile that is highly mediated by monocytes and macrophages in patients who have severity predictors. Older people have more significant oxidative stress naturally related to the ageing process; 2TDM and obesity present polarization to M1 macrophages, tending to inflammation via IL-6 and Th17. In addition to underlying tissue hypoxemia, heart failure also has more tissue hypoxia. All these underlying pathologies shift metabolism to oxidative stress and perpetuate a chronic condition of inflammation with continuous production of IDO-1 and stimulation of the Tryptophan anti-inflammatory pathway with an increase in the Kynurenine/Tryptophan ratio leading to a state of tolerance due to KYN act on AhR receivers [13,30,31].
The pathophysiology hidden in COVID-19 is complex because, in addition to the infection influencing metabolic changes with an impact on the immune response, it is pathophysiology dependent on inflammatory comorbidities, intensified by the hypoxemia of underlying diseases and by the hypoxemia induced by lung lesions and in other tissues caused by SARS-COV-2 [43][44][45].
The thin, young patient without comorbidities may have a tryptophan deficit, but their shift to innate immunity should still be minor, ensuring adaptive immunity in action against the virus.
Obese patients and T2DM with insulin resistance trigger immunosuppression due to the inflammatory tendency of the underlying disease, underlying hypoxemia, hypoxemia stimulated by COVID-19 and by serum serotonin. There is an intense shift of metabolism to oxidative stress, intensified by the tryptophan deficit causing NAD/NADH+ depletion, compromising the machinery of aerobic respiration.
In the elderly, even without comorbidities, metabolism is already shifted to oxidative stress, as ageing is inflaming. In addition, adaptive immunity is also impaired with a decrease in T lymphocyte receptors due to immunosenescence.
It is also generally known that innate immunity has a more glycolytic profile, whereas adaptive immunity is highly dependent on aerobic respiration and ATP.
Thus, we have that the hypoxemia triggered by SARS-CoV-2 associated with Try depletion by internalization of intestinal ACE-2 are factors that lead to the intensification of the innate immune response, especially in individuals already predisposed to oxidative stress. This deviation causes intense immunosuppression, and it can also be magnified by the action of serotonin and the tryptophan deficit [12,[46][47][48].
In yellow fever, deceased patients showed an increase in the Kynurenine/Tryptophan ratio. They showed a tendency to immunosuppression due to tissue hypoxemia. According to what is known about haemorrhagic shock in YF, it must have occurred due to DIC (disseminated intravascular coagulation), decreasing oxygen supply to tissues, producing adenosine, and shifting metabolism to oxidative stress [49,50].
In COVID-19, hypoxemia is already a fact given by the lung injury caused by SARS-CoV-2. Thus, all physiopathology of the host-parasite relationship is carried out amid hypoxemias. Consider that the more prolonged exposure to hypoxemia, the worse the immunosuppression, the tendency to innate immunity, and the oxidative stress pathway.
Both signatures promote a shift from innate to adaptive immunity, mediated by monocytes with differentiation into dendritic cells and macrophages. Monocyte distribution, based on CD14+ CD16+ does not have significant change in the number of classic monocytes (CD14 ++ 16-ve), but an increase in intermediate (CD14++ 16+) and non-classic (CD14+ CD16++) subsets in patients compared to healthy controls. Shown classical double expression of positivity for HLA-DR/CCR2 and HLA-DR/CX3CR1 in patients with COVID-19; however, CCR2 expression was reduced in the intermediate subset in patients with COVID-19. Monocytes are heterogeneous and are classified into different subsets defined by the extent of their cell surface expression of CD14 and CD16. The main subset, termed classical monocytes, consists of CD14highCD16negative monocytes (CD14++ CD16−), while monocytes expressing CD16 are generally divided into an intermediate CD14highCD16low (CD14++ CD16+) subset and a CD14lowCD16high (CD14+ CD16+) subset not classic subset. Differential expression of the chemokine receptors CCR2 and CX3CR1 is associated with these human monocyte subsets with the classic CD14 ++ CD16− subset predominantly expressing CCR2 and the nonclassical CD14 + CD16 ++ subset showing lower CCR2 expression and significantly higher expression of CX3CR1. CCR2 and CX3CR1 are two chemokine receptors that regulate the responses of myeloid cells, such as monocytes and microglia, during inflammation. CCR2 and its ligand are crucial for the recruitment of inflammatory monocytes, increasing the adhesion of monocytes to the endothelium leading to their exit to the site of inflammation and polarizing macrophages into cells of the M2 repair tissue. The expression of CX3CR1 in intermediate and nonclassical monocyte subsets indicates a more phagocytic phenotype and a greater likelihood of endothelial damage. These cytokines appear to play an important role in CNS inflammation during viral encephalitis since inflammatory monocytes secrete proinflammatory cytokines such as IL-6, IL-1β and TNF-α, which have been implicated in the development of acute seizures and hippocampal damage [28,39,[54][55][56][57].
In the gastrointestinal tract, mature gastrointestinal macrophages (GI-Mϕ) maintain the homeostasis site through their hyperresponsiveness to the secretion of regulatory cytokines, including IL-10, which maintain regulatory site T cells (Tregs). In inflammatory bowel disease, the profile of these macrophages presents the CD11highCCR2+ CX3CR1+ phenotype. The expression of IL-10 mRNA in CD14+ CD16− (classic monocytes), but not CD14 + CD16 + (nonclassical monocytes) responds to lipopolysaccharide (LPS) stimulation, while TNF-α, IL-1 and IL transcripts -6 were detected in both subsets; Intermediate monocytes produce the highest level of IL-12 and IFN-γ in the context of antigen presentation [8].
Dendritic cells also play an important role in innate immunity in COVID-19 and can be classified as plasmacytoid DC (pDC), myeloid DC (mDC) and monocyte-derived DC (MDDC). pDCs directly block viral infections, resulting in the elimination of the pathogen, express TLR-7 and TLR-9 that detect viral and bacterial nucleic acids, and positively regulate the expression of MHC molecules and activation markers that will allow the antigenic presentation to T cells. PDC has been reported to activate CD8+ T cells and exhibit a low ability to activate CD4+ T cells. pCD differs in pCD1 and pCD2. pDC1 exhibits an immature phenotype with low to undetectable MHCII expression and activation markers, whereas pDC2 highly expresses MHCII and CD86. It has been reported that pDC1 induces T-reg, while pDC2 promotes proinflammatory T cell differentiation. mDC is highly migratory and regularly travel from the periphery to lymphoid organs' T and B cell zones. At a steady-state or during infection, mDC regulates T cell functions. mDC are classified into two main populations based on the expression of CD141 (or blood DC antigen 3, BDCA-3) and CD1c (or BDCA-1 ): CD141+ DC (or cDC1) and CD1c+ DC (or cDC2). CD141 + DC have been shown to induce Th1, and CD8+ T cell differentiation, CD1c + DC has been found to generate not only Th1 but also Th2, Th17 and iTreg immune responses [58]. Mouse cDC2 cells have been reported as the primary inducers of the Th2 and Th17 immune response after antigenic stimulation. Mouse cDC2 produce IL-23 during infection, whether they are located in the lungs, skin or intestine.
Dendritic cells also play an important role in innate immunity in COVID-19 and can be classified as plasmacytoid DC (pDC), myeloid DC (mDC) and monocyte-derived DC (MDDC). pDCs directly block viral infections, resulting in the elimination of the pathogen, express TLR-7 and TLR-9 that detect viral and bacterial nucleic acids, and positively regulate the expression of MHC molecules and activation markers that will allow the antigenic presentation to T cells. PDC has been reported to activate CD8+ T cells and exhibit a low ability to activate CD4+ T cells. pCD differs in pCD1 and pCD2. pDC1 exhibits an immature phenotype with low to undetectable MHCII expression and activation markers, whereas pDC2 highly expresses MHCII and CD86. It has been reported that pDC1 induces T-reg, while pDC2 promotes proinflammatory T cell differentiation [40]. mDC is highly migratory and regularly travel from the periphery to lymphoid organs' T and B cell zones. At steady-state or during infection, mDC regulates T cell functions. mDC are classified into two main populations based on the expression of CD141 (or blood DC antigen 3, BDCA-3) and CD1c (or BDCA-1): CD141+ DC (or cDC1) and CD1c + DC (or cDC2). CD141 + DC have been shown to induce Th1, and CD8+ T cell differentiation, CD1c + DC has been found to generate not only Th1 but also Th2, Th17 and iTreg immune responses. Mouse cDC2 cells have been reported as the primary inducers of the Th2 and Th17 immune response after antigenic stimulation. Mouse cDC2 produce IL-23 during infection, whether they are in the lungs, skin, or intestine [21,[59][60][61].
MDDC prepared with LPS expresses high levels of IL-12p40 mRNA and secretes high levels of IL-12. CD16-MDDC expresses high levels of the CD83 DC maturation marker after TLR2, TLR3 and TLR45 binding. CD1c -CD11c+ CD16+ CD14− cells that massively produce TNF-α, IL-12 and iNOS and highly express TLR7 and TLR8. DC produces high IL-23, IL-1β and IL-6, which lead to the development of Th1/Th17 cells. Because they are Th1/Th17 cell inducers, MDDC has been reported to have the ability to cross-present to naive T cells and transfer peptides from MHC-I to DC residing in lymphoid. 5-HT signalling on DCs. 5-HT acting through 5-HT1 and 5-HT2 receptors induced chemotaxis in immature human DCs and increased DC migration from lung to lymph node drainage in mice. 5-HT increased the production of the proinflammatory cytokine, IL-6, and the Th2 cytokine, IL-10, while it reduced the Th1 cytokine, IL-12p70. Furthermore, DCs treated with M5-HT increased their Th2 production by attracting the chemokine CCL22 while decreasing the chemokine Th1, CXCL10 mediated by 5-HT4 and 5-HT7 receptors. 5-HT treated CDCs induced a Th2 polarization in naive CD4 T cells. 5-HT modulated the differentiation of DCs from human monocytes, increasing the production of IL-10 but reduced the antigen-presenting capacity. The involvement of 5-HT2B shifts the TNF/CCL2 ratio to the anti-inflammatory side in LPS-treated macrophages [43,[62][63][64][65].
The COVID-9 Th17 axis appears to be suppressed in severe cases. In patients with rheumatoid arthritis (RA) with dramatic disease showing an elevation of IL-6 and Th17, the levels of IL-1β and IL-18 directly correlate with IL-17. Inhibition of the IL-18/IL-18Rα signalling pathway inhibited the proliferation of autoreactive T cells and suppressed serum levels of IL-6, IL-18, TNF and IFN-γ. IL-18 is a cytokine of the IL-1 family proposed to promote barrier function in the intestine. IL-1 family cytokines are key co-regulators of CD4+ T cell fate, and the role of IL-1β in Th17 cell differentiation is mirrored by the contribution of IL-33 and IL-18 to Th2 and Th2 cell subsets. Although IL-18 is not essential for the differentiation of Th1 cells, in inflammatory conditions, IL-12 signalling promotes the expression of IL-18R1 in differentiating Th1 cells, after which IL-18 stimulation acts to increase the interferon production (IFN) -γ [66,67].
Based on an early review of the tryptophan listing and the articles on this metabolic flight, it offers yellow fever compared to what happens in COVID-19: 1-Critically ill patients evolve with a higher concentration of Kynurenine as metabolism is shifted to the inflammatory pathway.
2-In COVID-19, there is the internalization of intestinal ACE-2, with greater or lesser intensity depending on the amount in the inoculum, for example, or via (for example, upper respiratory tract or oral route), preventing the adequate uptake of tryptophan.
3-Lack of Try diverts metabolism to the kynurenine pathway and its metabolites, a pathway that is also influenced by vitamin B6.
4-Obese patients have serum serotonin due to insulin resistance. 5-Both Kynurenine and 5-HT have anti-inflammatory action and a tendency to immune response to Treg. 6-Hypoxemia and innate immunity to oxidative stress, as this pathway is preferentially glycolytic over adaptive, strongly dependent on aerobic respiration. 7-For this reason, we have two patient profiles, in general, in COVID-19: a) Insulin resistant or with some degree of previous hypoxemia or previous oxidative stress and b) Thin, young patients without comorbidities. Disease severity is related to the first group with a pre-existing inflammation profile. 8-Patients who express a tendency to the TH17 axis, with the production of IL-18, have a better evolution because they have a more inflammatory profile and are performed by adaptive immunity.
The depletion of tryptophan in COVID-19 patients due to the internalization of ACE-2 in the intestine promotes an unbalance of the immune response mediated by Kynurenine and magnified by 5-HT in patients with previous insulin resistance. The diversion of Tryptophan metabolism to the pathway of Kynurenine and its metabolites occurs due to Tryptophan shortage and hypoxia of the Disease and vitamin B6 deficiency, diverting metabolites for production of Kyn, HK, XA, and HaA. The action of Kynurenine, its metabolites, 5-HT, hypoxia, and the use of cathepsin L shift the metabolism to a tolerogenic environment, mediated by innate immunity, especially in critically ill patients. In Yellow Fever, there is no deficit in the absorption of tryptophan that triggers a more controlled cytokine storm, but still very lethal for those who develop tissue hypoxia resulting from DIC and shock. Those patients who present a profile tending to TH17 tend to have a better outcome, showing the importance of adaptive immunity in the viral and inflammatory control in the face of SARS-CoV-2 infection ( Figure 4). This Praeludium, which introduces this possible pathophysiological pathway, introduces the theme of making an analogy with a FUGUE. The themes are also covered in the Appendix in a complementary way to help understand the theory.

Methods
For this review, articles in English and Russian were allowed (with translation from abstract to English). The PubMed and Google scholar databases were used, the second being for theoretical complementation when necessary. Thus, it was a database used throughout the manuscript's production. There was no characterization of the minimum date for the articles. From the descriptors: "Yellow Fever and Tryptophan"; "COVID-19 and Tryptophan"; "AhR and immune response"; "5-HT and immune response"; "5-HT and thermogenesis"; "Kynurenine and immune response"; "5-HT and monocytes"; "monocytes and macrophages"; "Obesity and Thermogenesis"; "COVID-19 and Cytokines"; "Th17 and Il-18"; "Treg and cytokines"; the first 20 articles were selected, the abstracts were evaluated so that the 5 best by theme were chosen. The criteria used were adapted from the PRISMA protocol, at https://www.canada.ca/en/public-health/services/reports-publications/canada-communicable-disease-reportccdr/monthly-issue/2015-41 /ccdr-volume-41-04-april-2-2015/ccdr-volume-41-04-april-2-2015-3.html. Accessed in 02/09/2021. More 119 articles were add, during the writing, to embase the research.

Fugue
The results are organised by topics regarding SARS-CoV-2 physiopathology and effects in the COVID-19 patient considering management possibilities. More information about it is in the Appendix and in the other articles published before [3,68,69].

Tryptophan anti-inflammatory pathway and phenylalanine pathway
Based on tryptophan as exposed above there are the necessity of reposition and use of drugs that maintain 5-HT at a good base line to perform its activities on CNS without psychiatric symptoms. There are 2 Clinical studies that use Fluvoxamine, a selective serotonin reuptake inhibitor (SSRIs) [70][71][72].
Regarding Phenylalanine it is important to considerer using drugs to supply catecholamine underproduction to maintain dopamine replacement and catecholamine intake. For patients with parkinsonian symptoms or psychiatric symptoms, try to replace dopamine orally (Levodopa) or intravenously in case of critically ill patients or in refractory shock. Maintain low doses of noradrenaline concurrently sustained by vasopressin [73].
Consider that cytokine storm causes generalized glandular hypofunction, just as it does in sepsis. Furthermore, as the patient's metabolism is shifted towards oxidative stress, cortisol and catecholamines, there is an important demand that the lack of Phe substrate cannot meet [2].

Recommendation based on clinical research (Try) e specialist opinion
Prescribe: Citalopram 40 mg 1 time/day and Dopamine replacement.
In relation to tolerating higher CO 2 targets we must be careful not to allow low pH values. The adjustment of the pH must be done using the ventilator and, if necessary, use 8.4% sodium bicarbonate replacement to adjust the pH above 7.3. The expression of cathepsins at low pH also leads to immunosuppression by lymphocyte apoptosis. Diverting even more the microenvironment towards tolerance and permission to the development of neoplasms. More information on this topic can be found in an article recently submitted for publication "The Placental Buffer Effect and The Pathophysiology of COVID-19: Possibilities for a guide aimed at pregnant and postpartum women considering praxis: theory, clinical and laboratory observation".

Recommendations:
Manage the ventilator to try to adequate PaCO 2 values while prioritizing protective ventilation. Use 8.4% sodium bicarbonate to correct the pH so that it is always above 7.3.

Replacement of vitamin B complex and N-acetylcysteine (NAC)
Replacement of vitamin B complex and N-acetylcysteine (NAC)Vitamin B complex replacement is necessary since COVID-19 evolves with Pellagra and changes in the B3 (niacin) production pathway are related to Tryptophan deficit with impaired aerobic respiration and shift to oxidative stress requiring replacement of pathways that are antioxidants. NAC does not perform well against some oxidant species such as H 2 O 2 , O 2 • − , OHNOO, and HO•, but for others, including NO 2 and hypohalous acids, HOX, it could be more plausible. Hypochlorous acid (HOCl) and related species (hypobromous acid, HOBr; hypothiocyanous acid, HOSCN) are oxidants produced by activated neutrophils and monocytes through the activity of myeloperoxidase (MPO). Considering neutrophil chemotaxis due to the intense production of IDO-1, NAC replacement is necessary. NAC-derived cysteine is desulfurated to generate hydrogen sulfide. Also, NAC is necessary to the glutathione cycle. Furthermore, sulfane sulfur species produced by 3-mercaptopyruvate sulfurtransferase and sulfide. Some studies have been shown that quinone oxidoreductase are the current mediators of the immediate antioxidative and cytoprotective effects provided by NAC [58,[82][83][84][85].

Recommendations:
To prescribe N-acetylcysteine 600 mg/day Ascorbic acid 2 g/day If possible, prescribe Taurine.

Anticoagulants and antiaggregant: Serotonin thrombosis
Neutrophils play an essential role in platelet activation, and, in COVID-19, severely ill patients evolve with marked leucocytosis due to neutrophilia. There are many reasons for Neutrophilia to happen, and most of it is stimulated by the expression of cathepsins, mainly cathepsin G.
Neutrophils enhanced the aggregation of human platelets in vitro in a dose-dependent fashion, and this effect was diminished by pharmacologic inhibition of cathepsin G activity and knockdown of cathepsin G expression ( Figure 5).
Cathepsin G increased platelet surface expression of P-selectin (an activation-dependent neutrophil binding site), the glycoprotein IIb/IIIa complex (fibrinogen receptor), and glycoprotein IV (thrombospondin receptor), and decreased surface expression of glycoprotein Ib (von Willebrand factor) ( Figure 5) [86][87][88]. Serotonin has a mitogenic effect on megakaryocytopoiesis. This effect may be mediated via the 5-HT2 receptor, which is known to be coupled to G protein. Platelet α-granule constituents, including platelet-derived growth factor (PDGF), platelet factor 4 (PF4) and transforming growth factor-β (TGF-β), can affect megakaryocytopoiesis. Serotonin, a platelet dense granule constituent, has been shown to have a mitogenic effect on fibroblasts and smooth muscle cells, but whether it has the same effect. Circulating metastatic cells attract platelets and influence them to release their granule content acting in human NK cells losing their cytotoxicity and their ability to produce IFN-γ (interferon-γ), possibly through the downregulation of NK G2D ligand-mediated by platelet-TGF-β (transforming growth factor-β) release. Platelets' immune-modulatory potential is dependent on the underlying pathological conditions, as platelets from patients with dengue virus infection stimulate monocytes to produce MCP-1, IL-1β, IL-8 and IL-10 [89,90].
Myeloperoxidase (MPO) is the most abundant protein in neutrophils and represents 5% of their total protein content. MPO and neutrophil activation via CD11b/CD18 integrins, which is an indicator of MPO's possible contribution to neutrophil recruitment to the site of inflammation. A study shows that SARS-CoV-2, which we detected significantly higher expressions of MPO (~4 fold, p < 0.05) at the nasopharynx region, and speculates this neutrophil burst and even more overexpressed MPO may cause the production of excess hypochlorous acid (HOCl) and other reactive oxidants that also damage the nasopharynx tissue. Only MPO may be an important factor where the protective inflammation can become pathological in SARS-CoV-2 cases.
In previous work not yet published, I exposed the critical role of Adenosine in the pathophysiology of COVID-19. Adenosine is produced to antagonize mechanisms of cellular aggression, in the case of COVID-19, related to intense hypoxia caused by the viral attack, triggering lung lesions and other target tissues [91][92][93].
The most critical issue related to Adenosine is the production of ADP (adenosine diphosphate), which is a platelet activator and stimulates inflammation. Moments of support for this metabolic pathway, such as a low oxygen supply, can be stimuli for the maintenance of inflammation in the patient COVID-19. This fact is seen in clinical practice when lowering the O 2 fraction in patients, as they restart an inflammatory process with leucocytosis, increased LDH, D-dimer, for example.
The adenosine A1 receptor, which has a relatively high affinity for Adenosine, promotes neutrophil chemotaxis, and the A2A and A3 receptors are expressed at high levels on neutrophils, where they suppress neutrophil effector functions such as reactive oxygen species (ROS) formation when activated [94][95][96][97][98].
Dipyridamole inhibits NETosis and prevents thrombosis, in addition to acting to reduce inflammation. I have no experience with this drug, but I think a clinical study is needed as soon as possible. Prophylactic heparin or enoxaparin.
Acetylsalicylic acid 100 mg once daily.
All with Citalopram 40 mg, once a day for 30 days.

Anaemia
Initially, it was thought that anaemia in COVID-19 was due to hemophagocytic syndrome or Histiophagocytic Syndrome, but few cases present these associated diseases. This fact does not make any of the previous works unfeasible, as we are talking about science and something new to us, never seen before. Today it is one way; tomorrow, everything can change. The hypotheses must be launched and, it was from these studies, we had many important parameters to be seen in the laboratory tests of COVID-19 patients [14,99]. Iron is a cofactor of tyrosine hydroxylase and tryptophan hydroxylase, enzymes responsible for synthesising dopamine and serotonin, respectively. IFN-γ, one of the central cytokines of Th1 type immune response, activates IDO and neopterin formation in hematopoietic stem cells and influences the proliferation of various stem cell populations. The intravenous injection of neopterin into mice results in a prolonged decrease in the number of erythroid progenitor cells and an increased number of myeloid progenitor cells (CFU-GMs) by activating stromal cells. QUIN inhibits EPO production by stimulating the production of nitric oxide (NO) and inducing HIF-1α degradation. Trp metabolites like Kyn, on the other hand, increase hepcidin expression and inhibit erythropoietin (EPO) production by activating AhR. AhR competes with hypoxia-inducible factor 2α (HIF-2α), the key regulator of EPO production, for binding with HIF-1β. In the liver, serotonin represses hepcidin is through a 5HT2B receptor-dependent pathway, independently of any other known hepcidin regulators, including bone marrow signals. This regulation is conserved in humans and shows physiological significance as a negative correlation between serotonin and hepcidin levels [14,100].
In COVID-19, persistent anaemia seems to be related to: 1-Most seen in obese and insulin-resistant patients. Modification of Tryptophan metabolism in inflammation that is carried out by the IDO-1 enzyme. In SARS-CoV-2 infection, the production of IDO-1 is produced in large quantities and, for its formation, pyrrolic rings are needed, becoming in deficit for the construction of new erythrocyte molecules.
IDO1 is composed of two domains, among which the function of the N-terminus domain is still unclear and may help the stability of the system, while the large C-terminus domain contains the active heme centre performing the core functions of the enzyme. The C-terminus domain is rich in hydrophobic residues, which shows a component strictly to the shape of the indole ring of the substrate, allowing the interaction of oxygen molecule (O 2 ) with the iron atom (Fe) in the first step of the reaction. In the large domain, there is a ligand delivery tunnel for O 2 and water molecules (H 2 O), which extends along with the E and Fα helix to the active heme centre, as well as the 360-381 loop region controlling the shuttle of substrate/product in/out the catalytic site. The loop parallels with the heme plane before adding inhibitor but moves to the small domain (i.e., N-terminus domain) after the association with IDO1/ Try/kynurenine. The structural biology of IDO1 will be detailed described in the section [101,102].
Reinfusion of autologous hematopoietic peripheral blood stem cells (PBSC) or bone marrow is often accompanied by flushing, dyspnoea, abdominal cramping, nausea, and diarrhoea. These symptoms and the observation that they can be prevented by ondansetron, a selective 5-HT3 receptor antagonist, led to the assumption that these side effects are due to the infusion of free serotonin during the reinfusion of PBSC or bone marrow.
2-More seen in thin patients without insulin resistance. Tph1 as an erythroid gene: moreover, it uncovered a fundamental role for 5-HT in regulating the hematopoietic stem cell fate along the erythroid pathway. EPO induces TPH1 expression and 5-HT synthesis necessary for erythroid progenitors survival and proliferation. In purified human CD36+ cord blood cells, using qRT-PCR, we demonstrate that mRNA for TPH1, the 5-HT2A receptor (5-HT2AR-HTR2a), and the 5-HT-specific membrane transporter (SERT-slc6a4) were highly expressed at the specific pro-erythroblast stage of differentiation (day 3 of the culture after CD36+ isolation). These patients seem to develop some myelodysplasia; for this reason, it is vital to perform a therapeutic test with Citalopram and replace Tryptophane and, logically, to follow these patients properly, since the fact that SARS-COV-2 increases the expression of cathepsins is possible that neoplastic diseases are more likely to develop, especially considering a tolerant environment.
IFN-γ, one of the main cytokines of Th1 type immune response, activates IDO and neopterin formation in hematopoietic stem cells and exerts an influence on the proliferation of various stem cell populations. Trp metabolites like Kyn, on the other hand, increase hepcidin expression and inhibit erythropoietin (EPO) production by activating AhR. AhR competes with hypoxia-inducible factor 2α (HIF-2α), the key regulator of EPO production, for binding with HIF-1β. Well in line with this finding, Kyn/Trp and neopterin were shown earlier to be associated inversely with haemoglobin concentrations and positively with hepcidin concentrations in patients with HIVinfection before antiretroviral therapy. Antiretroviral treatment slowed down immune-mediated Trp catabolism and improved iron metabolism and anaemia [14].
It is necessary to be careful and attentive when administering Citalopram to type 2 diabetic patients with insulin resistance, as they may have symptoms like those seen in reinfusion syndrome, which occurs in autologous bone marrow transplants. In outpatient follow-up, I had the opportunity to witness the complaint of diarrhoea and abdominal pain after a week of the introduction of Citalopram.
I advise not to prescribe Citalopram for these patients, but it is essential to replace Tryptophane and melatonin. Usually, with these medications, the patient presents an improvement of symptoms related to the lack of intestinal absorption of the amino acid in question. It is important to ensure that these patients are not under the action of inflammation so that Try metabolism is performed via hepatic TDO.

Dysmetabolism, oxidative stress, uraemia and wasting syndrome by gluconeogenesis
The General and Integrated pathophysiology: SARS-CoV-2 marked the year 2020 because it caused the pandemic that is still ongoing in 2021. To date, we do not have any specific antiviral drugs, nor even other antiviral medicines that are effective. So far, we have only used corticosteroids to change the outcome of inflammation when used promptly, selective serotonin inhibitors and perhaps vitamin B3 supplementation, the anti-aggregating action of acetylsalicylic acid and anticoagulants such as heparin.
The disease is difficult to manage, and the explanation for this is that SARS-CoV-2 modifies some metabolic functions that imply the sum of multiple factors that support inflammation. Inflammation alters the microenvironment by shifting the balance of some reactions to the formation of undesirable by-products that are toxic to many tissues. COVID-19 is disease-specific to each person and, at the same time, bears similarities between the different patient profiles that we observe. We have a disease, the severity of which is related to inflammatory comorbidities, ageing and tryptophan reserves. After all, from the new evidence it is possible COVID-19 is a viral disease that evolves to a Tryptophan (Try) syndrome.
In general, SARS-CoV-2 infects any tissue that expresses the angiotensin-2 converting enzyme protein (ACE-2) on the surface of its cells. This enzyme is responsible for the balance of inflammation linked to angiotensin since the internalisation of ACE-2 provides greater availability of angiotensin II, which presents itself as an inflammatory agent by stimulating AT1 receptors (inflammatory) in cells of innate and adaptive immunity, adaptive in addition to favouring increased vascular resistance and increased aldosterone. However, there is an anti-inflammatory effect when it binds to the AT-2 receptor. Thus, we have an ACE/Ang-II/AT-1 results in increased pro-inflammatory cytokines, including IL-1, IL-6 and TNF-α, intensified by the activation of innate and adaptive immune and ACE2/ Ang-(1-7)/MasR axis down-regulation in the elderly, hypertensive, diabetic and cardiovascular compromised patient [1][2][3][4][5][6].
SARS-CoV-2 produces damage to the organs it passes through, and related injury presents generalized vascular endothelium injury, lung injury with airways inflammation and alveolar zones with hyaline membranes and type 2 pneumocyte hyperplasia, interstitial fibroblastic proliferation with fibromyxoid stroma, organising pneumonia, squamous metaplasia, and alveolar wall acute inflammation, diffuse hyaline membranes. This injury leads to hypoxemia. The internalization of the intestine ACE-2 stops capturing tryptophan, and the supply of this amino acid is now deficient for the formation of NAD/NADH+ (niacin) [20,21]. At the same time, interferon (IFN)-γ in dendritic cells (DC), macrophages, and monocytes due to IDO-1, while in a medium in homeostasis and without inflammation, metabolism tryptophan is carried out by the liver from TDO-1. This change provides for the diversion of the metabolic cascade towards Kynurenine production. Tryptophan metabolism via the KP results in a neurotoxin, quinolinic acid (QA), and a neuroprotective compound, kynurenic acid (KA). KA binds to the glutamate recognition site of the N-methyl-D-aspartate (NMDA) receptor and antagonizes it, while QA binds to the glycine site of the NMDA receptor with agonistic properties [22][23][24][25].
The most common and least severe side effects of niacin deficiency include depression, apathy, anxiety, headache, fatigue, disorientation, and memory loss. Severe niacin deficiency can cause a potentially fatal disease called pellagra. If left untreated, it can cause skin conditions, diarrhoea, dementia, and death. Niacin is part of many metabolic reactions in the body, so its depletion is related to the systemic symptoms present in COVID-19. Some studies report symptoms related to atherothrombotic mechanisms, as niacin can improve endothelial function, vascular inflammation, and vascular regeneration. Independent of correcting dyslipidaemia, niacin improves endothelial tube formation under lipotoxic and hypoxic conditions. Niacin improves HMVEC angiogenic function under lipotoxic and hypoxic conditions [8,[11][12][13].
Vitamin B3 can be formed by ingesting NA and Nam and by the tryptophan route. The intracellular pathway is reduced to NADH+, coexisting between the forms Nicotinamide adenine dinucleotide (NAD) and NADH+, or phosphorylated in NADHP, which is recycled or excreted. There are three ways to obtain NAD: Preiss -Handler pathway (PHP): NAD of nicotinic acid; via "de novo": tryptophan NAD and rescue route: Nam's NAD (Figure 1). NAD is an essential cofactor involved in many body reactions due to its reducing potential and participating in several energy metabolism pathways, including glycolysis, β-oxidation, and oxidative phosphorylation. NAD is a necessary cofactor for post-translation modifications, such as ADP-ribosylation and deacetylation by poly(ADPribose) polymerases (PARPs) and Sirtuins. NAD regulates energy metabolism, DNA damage repair, gene expression and stress response through enzymes. NAD(+) is the oxidised form of the nicotinamide adenine dinucleotide found in all living cells. In metabolism, NAD(+) is involved in redox reactions. NAD+ is degraded in the ADP-ribosyl transfer reactions as part of other noteworthy reactions. The lack of NAD is responsible for increasing neuronal degradation and the expansion of its precursor, nicotinamide mononucleotide (NMN), related to neuronal toxicity.
Some studies also show the role of nicotinamide (NAM) as an inducer of autophagy in cells of tissues injured by hypoxia by inhibiting the mammalian target of rapamycin (mTOR), so the cells can remain viable, avoiding apoptosis. mTOR pathway is a downstream target of the adenosine monophosphate-activated protein kinase (AMPK), and the regulation on this pathway exerts a substantial effect on cell viability. NAM can modulate cellular energy metabolism by regulating AMPK.
In the first days of infection, the inflammatory process initially inhibited by viral escape mechanisms starts to have its function normalised with the end of viremia because even if it escapes by inhibiting IFN-gamma and TNF, this process does not last more than 72 hours. There are cytotoxic lymphocytes that act against the virus and local defence cells, such as macrophages, dendritic cells, and monocytes. Therefore, damage to the vascular, pulmonary endothelium and other infected tissues already exists and causes respiratory and systemic consequences [3].
Structural changes in the organs infected by SARS-CoV-2 occur about D14 after infection or (D7 after the onset of the first symptoms). After this phase, the patient is symptomatic for 2 to 3 days without noticing hypoxemia or maintained hypoxemia with rare worsening. After this period, two paths are followed: an intense aggravation mediated by a neutrophil march in which the patient has a severe illness and often his condition is critical. Or the disease presents as moderate or oligosymptomatic forms. The release of CXCL8 (human homologue of murine chemokine CXCL2) by mononuclear cells, Sirtuin (SIRT6), and 5-HT are responsible for the neutrophil attraction.
Exposure to hypoxemia determines the consumption of NAD/NADH+, and its decrease in intracellular concentrations is responsible for the activation of the inflammatory response or even its exacerbation. The lack of niacin (NAD/NADH+) compromises aerobic respiration, while inflammation promotes the production of IDO-1 by phagocytes and platelet activation for the reconstruction of injured vessels tissues. Platelet activation is responsible for the release of serotonin, as it is one of the main reservoirs of this molecule in the human body. Hypoxia is an essential factor in the microenvironment commonly seen in many pathological contexts. DCs that reside in tissues and precursors of blood DC, including monocytes, can be recruited to sites of inflammation or solid tumour tissues that may be hypoxic. DCs in solid tumours are tolerant and in the joints of patients with RA inhibit adaptive Th1 cells while stimulating inflammatory Th17 cells. COVID-19 represents the struggle between tolerance and inflammation.
Tolerogenic DCs perform immunosuppressive functions through inhibitory molecules, such as programmed death-ligand receptors (PD-L1 and PD-L2), CD103, arginase, 2,3-dioxygenase indoleamine (IDO). Hypoxemia is fundamental to the patient presents immunosuppression due to COVID-19. The immunosuppression magnitude depends on the patient's time of exposure to hypoxemia. For this reason, "intubation in time" is part of the treatment to be offered to a profile of patient. Dendritic cells (DCs) can differentiate from monocytes via GM-CSF, IL-4 takes approximately seven days under normoxic conditions (21% O 2 ), and IDO-1 expression is upregulated in a hypoxemic environment. Hypoxemic tissue produces adenosine, an intermediate metabolite of nucleic acids. Adenosine is a key signalling molecule that orchestrates cellular response to hypoxia, energy depletion, and tissue damage by activating its G protein-coupled receptors (GPCR) on multiple cell types. The gamma interferon production stimulates the monocytes to produce IDO-1 and migrate to the injured tissue. They find adhesion factors and colony-stimulating factor (CSF-1), granulocyte-macrophage colony-stimulating factor, IL-3 and others. In tissues, monocytes are differentiated into macrophages and dendritic cells, which, together with the cells that reside in the tissue, play an essential role in eliminating pathogens. Circulating monocytes will differentiate into tissue macrophages that can be broadly classified into two groups: M1 macrophages after activation by IFN-γ or lipopolysaccharides (LPS) or M2 activated macrophages [103][104][105][106].
Maintenance of aerobic respiration is dependent on NAD/NADH+ dependent on exogenous niacin (Nam or NA) for their biosynthesis, and its concentration is inversely related to the production of TNF-alpha. For this reason, vitamin B3 has anti-inflammatory characteristics, as it acts in the replacement of NAD/NADH+. SIRT6 also plays an essential role in stimulating TNF-alpha expression [19,47,[107][108][109]. NAD+ is produced by the salvage pathway during hypoxemia and is metabolised by ectoenzymes to form adenosine (ADA) that regulates the immune response, promoting vasodilatory and antivascular endothelial leakage by increasing IDO-1 released by DCs. Hypoxia-inducible factor-1 (HIF-1 increases T-cell activation and alters cell metabolism favouring their differentiation to effector cells. IDO-1 inhibits cell proliferation and increases the p53 transcriptional targets p21 and TP53-induced glycolysis and apoptosis regulator. IDO decreases the transcriptional targets of both HIF-1α and c-Myc, hexokinase II and lactate dehydrogenase-A.

Serotonin and the magnitude of the disease: Glucose resistance -neutrophilia and hyperthermia versus neutropenia and hypothermia
It is necessary to consider that the COVID-19 severity occurs in people with comorbidities of an inflammatory profile but the greater intensity in obese, diabetic, and older adults. The first two are inflamed by adipocytes' characteristics producing inflammatory cytokines and in the elderly by immunosenescence with the natural increase in oxygen reactive and progressive loss of cellular repair mechanisms [110][111][112][113].
Serotonin (5-hydroxytryptamine, 5-HT) is a monoamine that mediates a range of central and peripheral functions. Synthesis of serotonin in both locations relies on the enzyme tryptophan hydroxylase encoded by two different genes, Tryptophan hydroxylase 1 (Tph1) and Tryptophan hydroxylase 2 (Tph2) expressed in the periphery and in the brain, respectively. Serotonin does not cross the blood-brain barrier, and thus each pool of this molecule has its distinct functions. In adipocytes, intestinal-derived serotonin (GDS) signals through the Htr2b receptor to favour lipolysis, increasing phosphorylation and hormone-sensitive lipase activity. In hepatocytes, GDS signalling through Htr2b promotes gluconeogenesis by increasing the activity of two rate-limiting gluconeogenic enzymes, FBPase and G6Pase. Also, GDS signalling in hepatocytes prevents glucose uptake in a manner dependent on Glut2, further favouring the maintenance of blood glucose levels.
Ang II induces its pleiotropic vascular effects through NADPH-driven generation of reactive oxygen species (ROS) that increase intracellular free Ca2+ concentration ([Ca2+]i), a major determinant of vascular reactivity. The key mechanism is the generation of ROS by serotonin degradation, catalysed by the mitochondrial enzyme MAO-A. Oxidative stress can act as a second hit in the pathogenesis, whereas lipid accumulation represents the first hit. In mitochondria, ROS induce damage to mitochondrial DNA30 and enzymes of the respiratory chain. Furthermore, they are potent inducers of the mitochondrial transition pore, leading to ultrastructural changes such as mitochondrial swelling, the formation of megamitochondria, cytochrome c release, and cell death. Lipid peroxides act as strong chemoattractant for neutrophils that are responsible for NETs and an intense ROS mechanism [114][115][116].
The oxidative stress could be a critical molecular linkage between the hypothalamic-pituitary-adrenal (HPA) axis dysfunction and mental disorders. The stress-induced increase in cortisol levels accelerates glucose metabolism and the production of reactive oxygen species. During stress, the hypothalamic-pituitary-adrenal HPA axis becomes critically engaged through its role in activating glucocorticoids' release, with consequent increases in heart rate, blood pressure, and metabolism. Acute release of cortisol during stress is responsible for enhancing cardiovascular function, mobilisation of energy, inhibition of growth and reproductive functions, and some immunological responses. However, glucocorticoid secretion's adaptive advantages during stress are limited to its acute rather than chronic release. Chronic elevation of cortisol is harmful, resulting in insulin resistance, visceral fat deposition, osteopenia and osteoporosis, inhibition of T helper-1 directed cellular immunity, and chronic suppression of the mesolimbic dopaminergic reward system. COVID-19 evolves severely in this patient profile. The accumulation of fatty tissue associated with chronic stress with insulin resistance provides an explosive environment that, at the expense of hypoxemia, consumes NAD/ NADH+ shifting the balance to an inflammatory process and even more dependent on beta-oxidation of fats. In these patients the large amount of peripheral serotonin is initially used for ROS production, which, when degraded, allows stored fat to be consumed in a thermogenic process that causes tissue damage and hyperthermia. Serotonin consumption leads to its lack of due to internalisation of ACE-2 and less tryptophan available.
Serotonin depends on reserves, so mast cells and platelet activation try to supply the physiological need for this molecule. A serotonin discharge may occur in each new platelet activation and symptoms of agitation, diarrhoea, and increased body temperature-Serotonin syndrome [32,117,118].
Vitamin B3 reserves are also depleted, and due to hypoxemia, MPO is inactivated, and Kynurenine has its products converted into NAD. However, the hypoxemic medium is the food for maintaining the beta-oxidation process that attracts more neutrophils -also chemo-attracted by activated monocytes. With each new tissue injury, a new activation of platelets and thus the inflammatory process is maintained. There are several neutrophil attraction mechanisms, but the maintenance of beta-oxidation associated with monocyte activation seems to play a dominant role since serotonin is depleted. However, in insulin-resistant patients 5-HT shows a significant role in the neutrophil marching [37,[119][120][121].

Thermogenesis b
Thermogenesis (TG) is frequent in patients with insulin resistance; they are severe and critical, usually in ICUs. These patients remain at elevated temperatures even with the use of antipyretic medications. TG occurs and causes a high temperature in the patients, not in fever but hyperthermia. These patients have excess serum serotonin, but it is quickly consumed and poorly restored due to the consumption of Tryptophan for the Kynurenine pathway, consumption of BH4 and Try deficit due to the internalization of ACE-2.
Insulin regulates plasma glucose levels by suppressing gluconeogenesis in the liver and inducing glucose uptake in skeletal muscle and adipose tissue. Obesity causes insulin resistance and glucose intolerance. The βcells overproduce insulin and augment their mass to compensate for insulin dysfunction. When it fail eventually results in type 2 diabetes. Plasma glycerol, produced by adipose tissue and used for gluconeogenesis, is not increased in gut-specific Tph1 during food deprivation [37,105,122,123]. 5-HT increases hepatic gluconeogenesis; it simultaneously decreases glycogen synthesis and reduces GLUT2mediated uptake of glucose. Exogenous 5-HT attenuates the thermogenic potential of the β-adrenergic receptor agonist, isoproterenol. 5-HT reduces cAMP levels in iBAT, lowers HSL activation, and reduces the expression of uncoupling protein 1 (UCP1), the mitochondrial protein responsible for thermogenesis). Peripheral 5-HT augments obesity by suppressing the "browning" of white fat, reducing UCP1 in BAT, and suppressing the secretion and expression of metabolically beneficial adiponectin [124][125][126].
Different mesenchymal progenitors form WAT and BAT, with BAT cells coming from progenitors common to the skeletal muscle tissue, which are favourable for myogenic factor 5 (Myf5), whereas WAT cells come from progenitors lacking this factor. A decrease in BAT activity is observed in individuals with obesity and type 2 diabetes, which is thought to exacerbate weight gain and metabolic disease by lowering energy expenditure [127][128][129][130].
Norepinephrine (NE) binds to β-3-adrenergic receptors (β3-AR) in adipocytes to activate thermogenesis. Cold causes the activation of specific channels located in thermoreceptor neurons innervating the body's, signalling for the release of NE. NE binds β3-AR activating adenylate cyclase, activating cAMP-dependent protein kinase A, promoting lipolysis and mitochondrial biogenesis by expressing several genes, including lipases, AMPK UCP1 and PGC1α [124,131,132].
Cold exposure increases the up-regulation and translocation of glucose transporters, glucose transporter (GLUT) 1 and 4, facilitating glucose uptake from plasma. This axis protects against hypertriglyceridemia, hyperglycemia and insulin resistance, which are common disorders associated with obesity. Additionally, cold exposure increases the production of vascular endothelial growth factor (VEGF), which enhances angiogenesis and provides a venue for heat dissipation.
There are a balance between leptin production and thermogenesis. Leptin may increase lipolysis and browning, although much less than upon SNS activation, and many of the hypothalamic neurons involved in the regulation of thermogenesis are also leptin sensitive. It appears that leptin has a double role in promoting browning and lipolysis, but after cold exposure, the decrease in leptin expression is compensated by other thermogenic drivers indicated before [124,133,134].
BAT is acutely activated by cold exposure via stimulation of the sympathetic nervous system (SNS), increasing BAT's intracellular cyclic adenosine monophosphate (cAMP) level. The high level of cAMP then increases protein kinase A (PKA)-mediated lipolysis of intracellular TAG into free fatty acids (FFA) to provide fuel for β-oxidation. FFAs also β-oxidize to generate acetyl coenzyme A (acetyl-CoA), which enters the tricarboxylic acid cycle and is oxidized to generate nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FADH2). The electron transport system then uses the NADH and FADH2 to produce a proton gradient. BAT uniquely expresses the uncoupling protein, Ucp1, which dissipates the proton gradient across the inner mitochondrial membrane, resulting in inefficiency during the formation of ATP in oxidative phosphorylation (OXPHOS). When Ucp1 is induced in the BAT, such as during cold stress or thyroid hormone (TH) stimulation, mitochondrial respiration is stimulated to the maximum amount to compensate for the gradient loss, generating heat in the process [44,[83][84][85]135,136].
Adipocytes express the insulin receptor and take up glucose via the insulin-stimulated glucose transporter type 4 (GLUT4) pathway, functioning as essential sinks of glucose, regulating systemic blood glucose levels. Selective deletion of the insulin receptor in UCP1-positive adipocytes has been reported to result in an age-dependent loss of interscapular BAT and systemic glucose intolerance in mice. Unlike white fat cells that solely rely on GLUT4 for glucose uptake, brown adipocytes can also take up glucose via the GLUT1 transporter in an adrenergic-dependent and insulin-independent manner. This mechanism involves the activity of nutrient sensor mTORC2 downstream of β3-AR signalling. The relative roles and modes of regulation of GLUT1 versus GLUT4-dependent glucose uptake in thermogenic fat in vivo will require further investigation [116,[137][138][139][140].
Notably, cold acclimation profoundly enhances systemic BCAA clearance preferentially in human individuals with active thermogenic fat. Consistent with observations in humans, cold exposure significantly reduced plasma Val, Leu and Ile in mice, but this effect was absent in mice with ablated thermogenic adipocytes. This BCAA sink function is an essential aspect of thermogenic fat function in glucose homeostasis because defective BCAA oxidation leads to diet-induced weight gain, glucose intolerance and insulin resistance in mice. In line with this, increased circulating BCAA levels, owing to reduced BCAA clearance, are linked to obesity, insulin resistance and type 2 diabetes in humans [124,133,138,139].
Since BAT has a high mitochondrial content, it is metabolically active and prone to oxidative damage. Increases in the level of reduced glutathione and activities of superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase suggest there is an elevated level of reactive oxidative species (ROS) in rat BAT during cold acclimation.
UCP1 is located in the mitochondrial inner membrane and uncouples the proton (H+) gradient from ATP synthesis. UCP1 activity is inhibited by purine nucleotides, whereas long-chain free fatty acids, which are negatively charged at the carboxyl end, bind to UCP1 and trigger the transfer of H+ into the matrix as a fatty acid anion/H+ symporter. One of the mechanisms of UCP1-independent thermogenesis in beige adipocytes is futile Ca 2+ cycling in and out of the endoplasmic reticulum. The Ca 2+ cycle involves Ca 2+ uptake into the endoplasmic reticulum by sarcoplasmic/ endoplasmic reticulum calcium ATPase 2B (SERCA2B) and its release by ryanodine receptor 2 (RYR2) and inositol trisphosphate receptor (IP3R), which is coupled to ATP hydrolysis by SERCA2B and heat generation. Activation of the α1-adrenergic receptor (α1-AR) and β3-AR, in response to norepinephrine, triggers cellular Ca 2+ flux and its futile cycling. Under certain conditions, such as increased cytosolic Ca 2+ levels (for example, enhanced Ca 2+ release from RYR2 or IP3R), ATP abundance (high ATP/ADP ratio) or reduced binding affinity of SERCA2 to Ca 2+ (often regulated by micro peptides), ATP hydrolysis by SERCA2 is uncoupled from Ca 2+ uptake, thereby being highly exothermic. Another UCP1-independent thermogenic mechanism is creatine substrate cycling, which involves ATP-dependent phosphorylation of creatine by mitochondria-localized creatine kinase (Mi-CK) to phosphocreatine (PCr) and PCr dephosphorylation by unknown diphosphatases (Enz1-n). Lipolysis of triglycerides (TAGs) generates glycerol and fatty acids, which can be re-esterified back to TAG (TAG-fatty acid cycling). This process involves ATP-dependent conversion of glycerol to glycerol 3-phosphate (G3P) by glycerol kinase (GyK). G3P is also a key component of the NADH-G3P shuttle, which involves interconversion of G3P and dihydroxyacetone phosphate (DHAP) and allows for rapid ATP synthesis in the mitochondria. This cycle is promoted by thiazolidinediones, which activate GyK and cold exposure and the satiety hormone leptin, which promote lipolysis. AAC, ADP/ATP carrier [125,139,[141][142][143][144].
5-HT does not cross the blood-brain barrier, and peripheral and central 5-HT represent two distinct pools. 5-HT regulates, via the hypothalamus, brain stem and the spinal cord, satiety, hepatic glucose uptake and adaptation to cold exposure is regulated by central 5-HT. Peripheral 5-HT produced by intestinal enterochromaffin cells, pancreatic islets, and adipose tissue exerts local or systemic lipid and glucose homeostasis control through distinct 5-HT receptors.
Central 5-HT promotes thermogenesis since pharmacological or genetic depletion of central 5-HT has impaired thermogenic adaptation to cold. It is related central depletion of 5-HT have reduced adaptation to cold exposure, diminished thermogenic function of BAT, and decreased recruitment of beige adipocytes. Central 5-HT appears to increase BAT and beige adipocyte thermogenic function by modulating sympathetic outflow to these tissues. Transynaptic retrograde tracing from BAT synaptic terminals shows glutamatergic and 5-HT neurons of the rostral raphe pallidus synapse onto sympathetic fibres in the intermediolateral nucleus (IML) of the spinal cord. Systemic or IML injections of 5-HT or fenfluramine increase the sympathetic firing of these fibres. In contrast, IML injections of 5-HT7 receptor antagonists decrease sympathetic tone. Central 5-HT pathways play a significant role in adapting to cold exposure through the sympathetic activation of thermogenic adipose tissue [4,5,13,29,40,49,54,[145][146][147].
The degradation of 5-HT is mainly catalyzed by mitochondrial monoamine oxidase A (MAO-A), generating 5-hydroxyindolic acid and reactive oxygen species (ROS), primarily H 2 O 2 . In addition to its role as a neurotransmitter in the regulation of central nervous system function, 5-HT also has multiple physiological functions in the periphery. 5-HT system, including 5-HT synthesis and 5-HT2 R, is activated in the hepatocytes of a T2DM mouse model, which crucially affected the occurrence of hepatic steatosis and inflammation with fibrosis. 5-HT2 R activation in hepatocytes regulates PKCε activation with the subsequent phosphorylation of Akt, mTOR, and ERK1/2, ultimately resulting in ELS, including de novo lipogenesis, and TG and VLDL synthesis with LDA, whereas the activation of both 5-HT synthesis and 5-HT2 R modulates oxidative stress with the activation of NF-κB and inflammatory signalling molecules, including p38, JNK, and STAT3 [31,40,124,144].
Serotonin promotes a fast stimulation in glucose uptake in both L6 myotubes and skeletal muscle mediated through the Htr2a receptor. The other thesis insists that incubation with serotonin-induced increased 2-deoxyglucose uptake in a concentration-dependent fashion by translocating GLUT4 to the cell membrane. GLUT4 translocation is caused by serotonylation of the small GTPase Rab4. In Serotonin signals 6-phosphofructo-1-kinase (PFK) through the Htr2a, the major rate-limiting enzyme of glycolysis and is related to the entire glycolytic pathway in the skeletal muscle.
Serotonin increases glucose uptake and glycolysis through Htr2a and intracellular serotonylation by stimulation of phospholipase C (PLC) in the skeletal muscle promotes the recruitment of protein kinase C (PKC) and calmodulin and the activation of calmodulin kinase II, which connects with PFK upon serotonin action [129,138,144,148,149].
Accumulation of the visceral WAT is highly associated with insulin resistance and diabetes. White adipose tissue (WAT) and brown adipose tissue (BAT) stores energy and generate body heat. WAT is stored subcutaneously and viscerally, surrounding intra-abdominal organs such as the liver, pancreas, and intestines.
Brown adipocytes have a common embryological origin with myocytes and are found mainly in humans' intrascapular, paraspinal, supraclavicular, suprarenal, pericardial, and para-aortic regions. Similar to muscle, it has a high concentration of mitochondria, which gives it a characteristic brown colour. The second population, known as "beige" or "bite" ("brown in white") adipocytes, is derived from a subpopulation of white adipocytes interspersed within the WAT. In humans, BAT is present at birth and regresses with age, although it remains metabolically active throughout adulthood. BAT is highly innervated and vascularized, rapidly responding to external stimulation such as cold and diet. BAT utilizes available substrates such as intracellular triacylglycerol (TAG) and blood glucose as fuels. Cold improves insulin sensitivity in patients with type 2 diabetes. Since cold acclimation can recruit the BAT in obese patients, BAT activation may also improve obesity-associated insulin resistance and hyperglycemia. The activity of adult brown and beige fat decreases with ageing and may contribute to the progression of chronic metabolic diseases. It appears that activating and recruiting brown and beige fat would be beneficial to improving overall metabolic health [124,125,133]. Thermogenesis in obese patients or patients with insulin resistance is something profound in patients infected with Sars-Cov-2. The mechanism proceeds as explained above. There is a 5-HT deficit due to Tryptophan malabsorption due to the internalization of ACE-2 in the intestine. There is the consumption of serum 5-HT, freeing space for the action of catecholamines, inducing UCP-1 in brown and beige adipocytes. Thermogenesis is one more stimulus to inflammation and the perpetuation of oxidative stress. Keeping the critically ill patient on high doses of norepinephrine amplifies this inflammatory pathway further, which is why it is necessary to associate vasopressin, trying to reduce the amount of norepinephrine supplied to sustain the blood pressure of the critically ill patient. Also, it is essential to remember that stress constantly stimulates cortisol and the release of adrenaline. However, these pathways are depleted due to the malabsorption of Tryptophan (serotonin) and Phenylalanine (tyrosine and catecholamines). Managing the patient COVID-19 is a great challenge due to the interference that the disease causes in multiple essential metabolic pathways in the control of immunity, inflammation and homeostasis ( Figure  6, Figure 7, Figure 8, Figure 9, Figure 10, Figure 11, Figure 12, Figure 13, Figure 14, Figure 15, Figure 16, Figure 17 and Figure 18).

Neopterin and tryptophan degradation
The metabolism of the amino acids Try, Phe and Tyr, support the hypothesis that low-grade inflammation is responsible for significant correlations found between immune system biomarkers like neopterin, KYN /Try or Phe/ Tyr. A link between increased KYN levels and an elevated KYN/Try is associated with accelerated Try breakdown due to activation of the enzyme IDO. Deprivation of TRP is an efficient strategy during the Th1-type immune response to counteract the unwanted proliferation of pathogens, infected cells and tumour cells. Immune activation and Phe/ Tyr results from the disturbed activity of Phe-metabolizing enzyme PAH due to insufficient supply with its cofactor BH4, which is sensitive to oxidation.
Kynurenine -a tryptophan metabolite that blocks antitumour immunity via Treg activation and Teff apoptosisinhibited T cell proliferation in a manner that BH4 can rescue. Accumulation of neuroactive kynurenine metabolites, such as quinolinic acid, may contribute to neurological/psychiatric disorders [61,150,151].
The biomarker most associated with tryptophan metabolites is neopterin, which had positive associations with KTR, kynurenine and anthranilic acid. Elevated levels of neopterin are associated with a pro-inflammatory state mediated by activation of the cellular immune system. It is an endogenous regulator of cytotoxic effects by activated macrophages and a potent peroxynitrite enhancer. It is a stable molecule eliminated only by the kidney. Higher levels are associated with higher reactive oxygen species and serve as an estimate of oxidative stress caused by the immune system. Th1-type IFN-γ and tumour necrosis factor-α may lead to an increase in neopterin, which is a biomarker of activated cell-mediated immunity. Neopterin was also negatively associated with tryptophan [152]. IL-10 is the most associated immune system biomarker, positively associated with kynurenine, KTR, 3-hydroxykynurenine and 3-hydroxyanthranilic acid. TNFα is negatively associated with tryptophan. Monocyte chemoattractant protein 1 is positively associated with tryptophan and, IFNγ is not associated with tryptophan metabolites. CD25+ Foxp3+ regulatory T lymphocytes are potent inducers of IL-10; this mechanism would allow kynurenine to exert a negative feedback loop on an initial acute inflammatory event and maintain a continuous balance between inflammation and immunosuppressive activity [28,49,54,73,132,133,153,154].
(6R)-5,6,7,8-tetrahydrobiopterin (BH4) is an obligate cofactor of nitric oxide (NO) synthases, playing a redox role in the catalysis of NO formation from L-arginine, O 2 and NADPH. BH4 is also a required cofactor for the phenylalanine, tyrosine and tryptophan hydroxylases. The biosynthesis of BH4 is dependent on the activity of the rate-limiting enzyme GTP-cyclohydrolase I (GTPCH I). EPO causes an increase in intracellular levels of BH4 via activation of GTPCH I. Inhibition of Jak2 abolishes EPO-induced BH4 biosynthesis, suggesting that increased phosphorylation and activation of Jak2 are the molecular mechanisms underlying the observed effect of EPO on BH4 synthesis. PI3K activity is an upstream activator of Akt1 because pharmacological and genetic inactivation of PI3K/Akt1 abolishes the stimulatory effects of EPO on GTPCH I activity and biosynthesis of BH4 in mouse aorta.
Inflammatory stimulation activates the inducible NOS, which increases the use of BH4 for optimal enzymatic activity and induces the formation of large amounts of oxygen radicals that contribute to the oxidative loss of BH4. Both increased use and loss of BH4 driven by a chronic inflammatory state may synergistically alter the function of BH4-dependent enzymes and then compromise the biosynthesis of monoamines, which may contribute to mood disorders. Thus, increased xanthurenic acid, a metabolite of 3-HK, has been shown to directly lower BH4 biosynthesis by inhibiting sepiapterin reductase. Concurrent upregulation of kynurenines and BH2 production may lead to a combined up-regulated activity of NOS (by kynurenines) and decreased availability of BH4. Such a combination results in an uncoupling of NOS and consequently reduced NO production favouring reactive oxygen species (ROS), which cause further oxidative BH4 loss.
Genetic inactivation of GTP cyclohydrolase 1 (GCH1, the rate-limiting enzyme in the synthesis of BH4) and inhibition of sepiapterin reductase (the terminal enzyme in the synthetic pathway for BH4) severely impair the proliferation of mature mouse and human T cells. BH4 production in activated T cells is linked to alterations in iron metabolism, mitochondrial bioenergetics and blockade of BH4 synthesis abrogate T-cell-mediated autoimmunity and allergic inflammation and enhancing BH4 levels through GCH1 overexpression augments responses by CD4+ and CD8+ expressing T cells, increasing their antitumour activity in vivo [8,13,61,157].
These inflammatory/anti-inflammatory pathways are related to the development of mood disorders and neurological diseases. Disruption of monoamine metabolism leads to several neurological manifestations in childhood that are evident in the clinical history and physical examination. The presentation of disorders can include cognitive and motor delay, epilepsy, autonomic dysfunction (which manifests as sweating, temperature dysregulation, hypersalivation and nasal congestion) and neuropsychiatric features such as anxiety or autism spectrum disorder. Motor symptoms are often prominent and include gait disturbances, dystonia, dyskinesia, parkinsonism, tremor, oculogyric crises, eyelid ptosis, and axial hypotonia; motor symptoms become more prominent at night and improve after sleep. Other associated features include feeding difficulties and microcephaly. Many clinical features of monoamine neurotransmitter disorders are seen in other neurological conditions, such as cerebral palsy, primary movement disorders, paroxysmal disorders, hypoxic-ischemic encephalopathy, and epileptic encephalopathies ( Figure 19, Figure 20, Figure 21 and Figure 22).

Statins
Mechanism of action is inhibition of HMG-CoA reductase, the rate-limiting enzyme of cholesterol synthesis. Inhibition of this enzyme interferes with the synthesis of mevalonate and isoprenoid intermediates, particularly farnesyl pyrophosphate (FPP) and geranylgeranyl pyrophosphate (GGPP), which are responsible for the isoprenylation of a wide range of proteins including small proteins associated with guanosine triphosphate (GTP) such as Ras, Rho and Rac. Isoprenylation of these molecules is essential for the covalent attachment, subcellular localization, and intracellular trafficking of membrane-associated proteins. Inhibiting the synthesis of isoprenoid intermediates may underlie many statins' pleiotropic effects, including their antioxidant and anti-inflammatory action. Statins also manifest immune-modulatory effects by activating regulatory T cells (Tregs). For example, in a murine model of tumour growth, statins activate Treg and increase the production of the immune regulatory markers IL-10 and TGF-β1. Statins reduce the number and increase the suppressive function of Treg cells in experimental animal models of chronic immune activation and humans with or without immune-mediated conditions. The production of Tregs is linked with the production of reactive oxygen species (ROS) geared at a minimum toward eliminating pathogens, at most, to regulate the balance between proinflammatory and regulatory arms of the immune response. This has a narrow regulatory window as specifically unopposed ROS production can suppress regulatory T cell production favouring proinflammatory reactions, or tiny ROS production may also impair Tregs' differentiation, stability, and suppressive function.
Statins reduce the production of kynurenine and actively limit the effects of kynurenine's main excitotoxic metabolite, QA. For example, in a model of QA-induced neurotoxicity in rats, statins significantly decrease the excitotoxic effect of QA, levels of markers of oxidative stress, and proinflammatory cytokines (such as TNF-α) as well as striatal lesion volume. In another study, statins appear to have a neuroprotective effect in excitotoxic rodent seizure models. Specifically, atorvastatin significantly reduced QA-induced clonic or tonic seizures and prevented cell death induced by QA in the hippocampus. Atorvastatin also counteracts the decrease in glutamate uptake triggered by QA and prevents the QA-induced decrease in protein kinase B (PKB, or Akt) phosphorylation.

Recommendation
To prescribe:

IgM and IgG bizarre profile in COVID-19 and vaccines
I assume that we are in a pandemic, so mathematically, those who have not had COVID-19 will still have it, and those who have, unfortunately, can have it again.
We are used to facing diseases with a similar pattern regarding the production of immunoglobulins (IgM and IgG), but it is strange to observe, for example, a family with 5 people sharing the same house. One of them is infected. All other people had contact with the index case, but 2 were asymptomatic, one was oligosymptomatic, and the other had to be hospitalized.
After 14 days, the formation of antibodies is bizarre. Sometimes the one who presented the formation of antibodies was one of the asymptomatic family members.
We must not forget that 60% of cases are asymptomatic or go unnoticed by the patient.
As we have seen, SARS-CoV-2 causes changes in the immune response from its entry into the cell, acting on cathepsins and furins, shifting the tryptophan axis to the Kynurenine pathway. Severe cases have presented intense lymphopenia with apoptosis of CD4+, CD8+, NK (natural killer) and B cells. This apoptosis varies from person to person due to its comorbidities and genetic variations. For example, some studies demonstrate that women have a higher prevalence in forming antibodies to COVID-19, relating to the fact that the innate immunity gene is contained in the X chromosome. Men have a single X; women have two X chromosomes, so they need to be silenced. The pattern of "silencing" occurs in such a way as to form a mosaic, with the woman having functioning X chromosomes of both maternal and paternal origin. This fact seems to promote more significant variability in the identification of pathogens and antibody production.
What seems to happen is that we produce antibodies, but often at low titers that are not identified by the usual tests. That would be the explanation for such a good response to the first dose of the vaccine against SARS-CoV-2. In other words, the first dose was a booster for many people who had COVID-19 but with negative serology.
Another important fact is that most of the cases admitted to the hospital ICU where I work had two doses of the vaccine, which did not prevent them from developing the severe disease.
We must remember that IgG is suitable when it is formed in sufficient quantity to neutralize the virus. Often, little IgG production can cause the phenomenon of infection amplification by the Antibody-dependent enhancement mechanism.
Once I understand that the virus causes immunosuppression, we must re-evaluate the issue of vaccination in patients who have severe disease. Will this patient respond to the vaccine in a good way, or could it be that they will have significant side effects, thinking that the pathophysiology of the disease can promote the development of autoimmune diseases that can be reinforced with vaccination? I believe that, above all, people's safety must prevail. Producing vaccines without knowing how the virus works may not be appropriate. I am not against vaccines, but I am in favour of people undergoing safe and effective vaccination.

Corticosteroids are not controversial
The use of corticosteroids is not controversial when used at the correct time. In the acute phase of the disease, the best period to be used is in the defervescence phase (between D6 and D8 with CPR < 10), avoiding the neutrophilic march that will start the cytokine storm. Corticosteroid pulse at this stage blocks disease progression in patients with predictors of severity and orotracheal intubation is avoided (Figure 23).
In the chronic phase and in refractory shock, corticosteroid pulses have also been the solution, as blocking inflammation has reversed the unusual causes of vasoplegia, noting that patient COVID-19 has a lack of catecholamines, vasodilatation by adenosine and large production of nitric oxide [69,122,123].
Thus, the patient in inflammatory shock should maintain norepinephrine and vasopressin, dopamine (if possible all in low doses) and perform a corticoid pulse, with preference for Methylprednisolone.

Discussion
COVID-19 is a mysterious disease, as it can simulate signs and symptoms of other known diseases, making its diagnosis difficult, especially in the chronic inflammatory phase of the disease called "Long COVID-19 Syndrome". The disease progresses with a viral infection for about 14 days, and the patient starts symptoms between the fifth and seventh days of infection; therefore, lung lesions and other infected organs have already occurred. After the seventh day of symptoms, few viruses remain, except those that may have predictors of severity (insulin resistance, age, and other inflammatory diseases). Between the sixth (D6) and the ninth (D9), the defervescence phase occurs -as also occurs in yellow fever, passing to the convalescence phase or to the toxemic/immune-mediated phase, responsible for the great aggravation that can lead to acute respiratory failure.
Proteomic and genomic studies have demonstrated the activation of innate immunity in patients who progress with severity, while adaptive immunity still plays a fundamental role against the virus in patients who evolve oligosymptomatic or asymptomatic.
CXCL8, CXCR1 and CXCR2 for neutrophil activation and accumulation, and inflammatory response genes (TLR4 and TLR6) associated with toll-like receptors and several significant inflammatory response genes (MMP8, MMP9, S100A12, S100A8), T cell activation, leukocyte-mediated cytotoxicity, natural killer (NK) cell-mediated immunity, and interferon (IFN)-gamma production were explicitly decreased in critically ill patients compared to groups that evolved without severity. Essential genes for T cell activation, such as CD28, LCK and ZAP70, and key transcription factors for the production of IFN-gamma (GATA3, EOMES and IL23A) are also low in critical patients. In addition, digital cytometry estimation revealed lower numbers of T and NK cells in critically ill patients. Protein polyubiquitination and autophagy increased gradually from asymptomatic to mild/severe and peaked in the critical group. An important coding factor gene for FOXO3 autophagy is also displayed in this expression pattern. Excessive activation of neutrophils can abnormally differentiate into pathological low-density neutrophils with an increased ability to release extracellular neutrophil traps (NETs). Excessive release of NETs causes endothelial damage, promotes thrombosis and contributes to mortality in COVID-19. Transcription analysis showed that neutrophils were significantly enriched in asymptomatic patients and slightly increased in critically ill patients. However, most proteins, including those involved in inflammatory pathways (CHI3L1, S100A8, S100A9, S100A11 and S100A12), neutrophil degranulation (ANXA3, FGL2, LRG1, PGLYRP1, DEFA1B and SLPI) and NETs (MPO and ELANE), were deficient in asymptomatic patients and increases progressively with disease severity. Notably, myeloid leukocyte activation and neutrophil degranulation pathways were enriched in these genes, further supporting the remarkable heterogeneity of neutrophils across different disease severity groups [21,28,50,60,61,150,[157][158][159][160].
Try degradation products, deplete T cells, increase apoptosis of T helper (Th) cells and NK cells, and promote T cell exhaustion. L-arginine is essential for T cell proliferation and function, and the release of arginase (ARG1/2) from activated neutrophils inhibits T cell activation by inducing depletion of L-arginine and glutamine. ARG1 and ARG2 levels were up-regulated in critically ill patients. Consistently, L-arginine, N-acetylornithine and L-glutamine decreased in critically ill patients. Exhaustion markers, e.g. CTLA4, BTLA, HAVCR2, ICOS and PDCD1, were significantly up-regulated in critically ill patients. Multiple upstream IFN molecules, including TLR3, IRF1, IRF7, MAVS, DDX58, TBK1, JAK1 and STAT2, were down-regulated in symptomatic, especially critically ill patients.
Patients with severity predictors change the immune response to innate immunity with tryptophan metabolism facing the Kynureninne pathway -highly immunosuppressive -and based on interleukin 10 (IL-10) and regulatory T cells making the microenvironment tolerant, tumorigenic and immunoparalyzed. Monocytes/macrophages and DCs are concentrated in the production of IL-6, IL-10, TGF-1b, and neopterin, allowing the formation of the BH4 enzyme, whose function is to reduce the intensity of oxidative stress the formation of NO.
However, the BH4 pathway is compromised due to the action of Kynurenine products. Furthermore, the intestinal internalization of ACE-2 decreases the Try and Phe supply, negatively impacting the formation of catecholamines and serotonin [40,67].
The action of Patients with high serum 5-HT levels will have even more severe immunosuppression with neutrophilia and hyperthermia due to thermogenesis. Thin patients without insulin resistance or inflammatory comorbidities evolve with hypothermia and leukopenia resulting from the acute lack of serotonin. These facts are dependent on the inoculum to which the patient was exposed and gastrointestinal involvement by SARS-CoV-2. Furthermore, the permanence of a hypoxemic environment with adenosine production allows for a further shift of immunity towards the axis of tolerance and bradycardia [94,96,161].
The oxidative stress axis is fed by multiple pathways: more inflammatory environment due to internalization of ACE-2, hypoxemic environment, impediment of the action of BH4, consumption of NAD/NADH+. Thus, the signature of inflammation in critically ill patients is represented by innate immunity, serotonin and oxidative stress ( Figure 24).

Conclusion Conclusion and ethical issues
COVID-19 is a viral disease that has caused many disorders in people's lives. It is an absolute catastrophe in both the acute and chronic phases. The acute phase still has the same treatment protocols since the beginning of the pandemic, and patients continue to evolve to death. Although we still do not have the results of large trials, studies from research centres and quality hospitals show the benefit of using some drugs, such as selective serotonin reuptake inhibitors. Furthermore, recognizing thermogenesis allows its treatment with an insulin pump. At a critical moment such as this pandemic, ethical issues must be related to the intention to do something different; however, it is based on profound and reliable studies. It is not unethical to use a drug as long as it is well studied and supported by the literature when people are dying in the same way.
The chronic phase, "The Long COVID-19", has been an unprecedented catastrophe. Patients, mainly the elderly, are admitted to hospitals with acute delirium or with an acute change of consciousness without image changes in computed tomography of the skull. However, when researched, it is common to find pulmonary images of previous COVID-19 sequelae, increased LDH and a generalized inflammatory profile with urine showing proteinuria and hematuria, sometimes with ketone bodies. This condition is often associated with weight loss. Usually, these patients have been diagnosed with some neoplastic disease-causing wasting syndrome (this can occur since the patient is immunosuppressed by . However, the condition can often be reversed using corticosteroids and vitamin B complex replacement, L-Dopa replacement, and the use of serotonin reuptake inhibitor.
I have been following patients undergoing "The long COVID-19", and the complaints are the same: pain in the calves, hair loss, exacerbation of pulmonary or upper airway conditions, or abdominal conditions ranging from tenesmus and diarrhoea. These conditions have had an excellent response to the use of corticosteroids, ondansetron and tryptophan and B complex replacement. I always tell patients that everything is still theoretical and that I also have many doubts, so we always build the therapeutic plan together. Nevertheless, I reinforce that the patient is always well informed about everything, including my doubts about something new like SARS-CoV-2. So far, I have not had cases that worsened due to the use of these drugs; on the contrary, there was an essential improvement in symptoms, improving patients' quality of life.
We have to be careful because in a pandemic, mathematically, those who are not infected will still become infected, and, in the case of SARS-CoV-2, those who are already infected can become infected again. Thus, COVID-19 should be included in the diagnostic hypotheses whenever conditions might suggest an underlying inflammatory cause or something new that did not exist in the patient before. The start could have been COVID-19.
We cannot see SARS-CoV-2 as simple. This new adversary needs to be studied and well understood to act in the best possible way and the consequences left by him in people. We have to recognize our ignorance and study because our knowledge is limited and to think that we already have all the answers to the unknown is to be antiscience. It is stopping the search for knowledge since what drives us are doubts and questions.

Final Considerations
In the beginning, the article proposed the pathophysiology of this probable COVID-19 based on news publications showing the presence of tryptophan metabolites via the immunosuppressive pathway of Kynurenine in patients who died from yellow fever. The clinical changes seen over almost two years of follow-up of COVID-19 patients, aided by laboratory tests, allow the comparison between the two diseases, reinforced by neuropsychological and immunological clinical symptoms and by laboratory tests that, in greater magnitude, show neutrophilia in patients who progress to death in both diseases.
These latest published studies helped to understand a possible explanation for the evolution of the disease in obese, diabetic and elderly patients, especially.
It turns out that, unlike Yellow Fever, COVID-19 perpetuates a much more exuberant and prevalent inflammatory status, activated by multiple pathways and feedback.
Chronic COVID-19 is a Thrombo-metabolic Syndrome, tolerant and immunosuppressive, whose intensity varies from person to person, but it is more intense in critically ill patients or who were once in patients in ICUs. Chronic inflammation can appear at any time -near the acute phase or farther away. It is essential to understand if the patient is inflamed in its entirety, presenting systemic changes. "The Long COVID-19" mimics bacterial sepsis but responds poorly to the use of antimicrobials. It is necessary to stop the inflammation using corticosteroids, but antimicrobials are necessary due to the intense bacterial translocation through the intestine and the skin.
The pulmonary image is usually sequelae with pleural effusion and posterior atelectasis in the lung bases, laminar atelectasis, consolidations forming something like nodules or images confused with fungal or mycobacterial infection. This type of formation is seen in rheumatologic and inflammatory diseases and is called organizing pneumonia.
Diagnosing "The Long COVID-19" is difficult, but few tests can help with the diagnosis.
1. COVID-19 is a SARS-CoV-2 infection that triggers an automatic inflammatory feeding loop by tryptophan (Try) deficiency due to the internalization of ACE-2, causing an imbalance in the inflammatory pathway by the immune response against SARS-CoV-2 and the anti-inflammatory pathway mediated by Kynurenine (KYN).

Maintaining hypoxemia creates a tolerant and tumorigenic microenvironment.
3. Niacin is essential for aerobic respiration to occur. In its absence, the tryptophan pathway tends to alter the balance for the formation of B3. However, in the tryptophan pathway, inflammation, via IDO-1, tends to metabolize kynurenine by-products -toxic and immunosuppressive. One of the products of hypoxia is adenosine, whose effect is anti-inflammatory, and its overproduction due to severe hypoxemia may explain bradycardia as the main arrhythmia of COVID-19 and the myocardial damage caused by a cytokine storm. 5. Thrombosis in COVID-19 may be the primary cause of high serotonin levels (5-HT) in obese or glucoseresistant patients.
6. Thrombogenesis takes several ways, but it needs to act on the cause and not just on the phenomenon to overcome thrombogenesis. Inflammation and hypoxemia must be blocked so that anticoagulant or antiplatelet therapies are not refractory.
7. These pathways (NAD/NADH+, expression of furins and cathepsins) show that we should not keep the patient hypoxemic, and sometimes IOT is mandatory.
8. The intense production of adrenaline stimulated by a highly stressful environment triggers an exacerbated thermogenesis after the consumption of serotonin, which starts to express UCP-1.
9. Thermogenesis produces tissue damage and chronic inflammation in patients with COVID-19.
10. Corticosteroids are still a good weapon against a disease that causes inflammation through multiple pathways. The strength of corticosteroids in COVID-19 lies in the fact that they are non-specific. Thermogenesis blockade is essential in the clinical management of critically ill patients COVID-19.