Early Subcutaneous Immunoglobulin for X-Linked Agammaglobulinemia

Introduction: Subcutaneous immunoglobulin (SCIG) utilization is limited in Spain. Our aim was to describe our experience with SCIG from the diagnosis in a patient with X-linked agammaglobulinemia (XLA). Case Presentation: A recently diagnosed 6-year-old child with XLA was started on SCIG. A loading dose of 6 g, in three consecutive days (2 g/day) was prescribed. Initially, the aim was trough serum IgG over 500 mg/dL. Nevertheless, 15 months later, IgG levels fell below 500 mg/dL, and some infections occurred. A new aim of IgG over 700 mg/dLwas established, after current recommendations. Dose was increased to 3 g every 7 days. IgG levels rose over 700 mg/dL, and infections disappeared. Parental evaluation of quality of life is good. No adverse events were reported. Conclusions: SCIG is a valuable choice for treating XLA patients, even from the very beginning.


Case Report
A 6-years old male was attended in May 2012 at the Pediatric Infectious Diseases clinics for recurrent infections (diarrhea and chronic suppurative otitis media).He was the first kid of 2 siblings.Her sister was a 4-year-old healthy girl.There was no antecedents of suspected or confirmed immunodeficiency in any part of the family tree.There were no deaths at an early age in grandparents, uncles, aunts or cousins.
Upon suspicion of primary immunodeficiency with concurrent infections, immune study was requested.The study of immunoglobulins by turbidimetry showed the following results: IgG 458 mg/dL, IgA < 33 mg/dL (verified by nephelometry: high sensitivity IgA < 6 mg/dL) and IgM < 21 mg/dL.A mutation was found in the BTK gene (located in Xq22.1).Laboratory tests confirmed a profoundly diminished (15%) expression.B cell levels were 0.34% CD19 +.After deliberation with the parents, we decided to start on SCIG 20% (Hizentra ®, 200mg/mL, CLS Behring, Marburg, Germany), by infusion pump.The initial goal was to keep IgG over 500 mg/dL, following recommendations [1].An initial loading dose of 6 g (322 mg/kg) was administered over 3 consecutive days, at 2 grams daily (107 mg/kg/day).The first three doses were administered in the hospital daycare facility, without premedication.During these three days, the parents were trained in infusion technique.There were no complications.The following doses were administered at home, at a rate of 2 g every 7 days (107 mg/kg/week, 428 mg/month) (Figure 1).An analysis on day +10 showed that levels of IgG were 869 mg/dL.Infusion was changed to 2 g every 10 days (321 mg/month).The following +10 levels were 465 mg/dL, so we returned to 2 g every 7 days (428 gr/month).

Introduction
X-linked agammaglobulinemia (XLA) or Bruton agammaglobulinemia, is an inherited immunodeficiency disease caused by mutations in the gene BTK, that codes for Bruton tyrosine kinase (BTK).In the absence of BTK, B lymphocytes do not differentiate or mature.Without mature B lymphocytes, antibody-producing plasma cells are also absent.Therefore, XLA is characterized by low levels of serum immunoglobulins and almost total or total absence of B lymphocytes and plasma cells.
The current management is the immunoglobulin replacement therapy (IRT).Traditionally, IRT has always been performed with intravenous immunoglobulin (IVIG) every 2-4 weeks.Currently, subcutaneous immunoglobulin (SCIG) is also available.Utilization of SCIG it is still limited in Spain.Physicians are often unfamiliar with its use, and availability is limited at many hospitals.Generally, the use of SCIG is sequential, after a loading dose IVIG.
In this case report, we review the case of a school-age boy with XLA, who was successfully treated with SCIG from diagnosis.