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. 2008 May;152(2):274-9.
doi: 10.1111/j.1365-2249.2008.03620.x. Epub 2008 Mar 12.

Rapid subcutaneous immunoglobulin administration every second week results in high and stable serum immunoglobulin G levels in patients with primary antibody deficiencies

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Rapid subcutaneous immunoglobulin administration every second week results in high and stable serum immunoglobulin G levels in patients with primary antibody deficiencies

R Gustafson et al. Clin Exp Immunol. 2008 May.

Abstract

Subcutaneous immunoglobulin G (SCIG) infusions as life-long replacement therapy in patients with primary antibody deficiences (PAD) is being applied increasingly. However, only a few published pharmacokinetic studies are available for this route of administration. Therefore, the pharmacokinetics of a 16% immunoglobulin G (IgG) preparation intended for subcutaneous use were investigated in patients with common variable immunodeficiency and X-linked agammaglobulinaemia. SCIG infusions (200 mg/kg body weight) were administered to 12 adult patients every 14 days for 24 weeks (total of 144 infusions). Pharmacokinetic parameters were determined based on serum IgG trough levels and antibody levels against tetanus. The median half-life of the total serum IgG and for the tetanus antibodies was 40.6 and 23.3 days respectively. Median in vivo recovery of serum IgG and tetanus immunoglobulins were 36% and 46% respectively. Median, preinfusion serum IgG trough levels per patient were high without major variations between infusions and ranged from 7.24 to 7.86 g/l. Safety, in terms of adverse events including systemic adverse reactions and local tissue reactions at infusions sites, was monitored throughout the study. Six mild, local tissue reactions were observed during the study in one patient. No systemic adverse reactions related to the study drug were observed and no serious other adverse event occurred during the study. It is concluded that the bi-weekly SCIG therapy was well tolerated in the study and that it results in high and stable serum IgG levels, offering an alternative therapy regimen to patients suffering from PAD.

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Figures

Fig. 2
Fig. 2
Increase in total serum immunoglobulin G (IgG) trough level over baseline after subcutaneous infusion (medians, interquartile spreads and ranges) for the pharmacokinetic phase of 14 days (normalized values shown).
Fig. 1
Fig. 1
Serum immunoglobulin G (IgG) trough levels (medians, interquartile spreads and ranges) over the study period of 24 weeks.

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References

    1. Primary Immunodeficiency Diseases. Report of an IUIS Scientific Committee. Clin Exp Immunol. 1999;118:1–28. - PMC - PubMed
    1. Eibl MM, Wedgwood RJ. Intravenous immunoglobulin: a review. Immunodef Rev. 1989;1(Suppl.):1–42. - PubMed
    1. Gardulf A. Immunoglobulin treatment for primary antibody deficiencies: advantages of the subcutaneous route. Biodrugs. 2007;21:105–16. - PubMed
    1. Gardulf A, Hammarström L, Smith CIE. Home treatment for hypogammaglobulinaemia with subcutaneous gammaglobulin by rapid infusion. Lancet. 1991;338:162–6. - PubMed
    1. Gardulf A, Andersen V, Björkander J, et al. Subcutaneous immunoglobulin replacement in patients with primary antibody deficiencies: safety and costs. Lancet. 1995;345:365–9. - PubMed

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