Functional Activities of Various Preparations of Human Intravenous Immunoglobulin Against Type III Group B Streptococcus
- 1 June 1986
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Infectious Diseases
- Vol. 153 (6) , 1092-1097
- https://doi.org/10.1093/infdis/153.6.1092
Abstract
Two preparations of human immunoglobulin modified for intravenous use (iv immunoglobulin) by different methods (reduction-and-alkylation, or pH 4 treatment) were evaluated for in vitro and in vivo activity against a strain of type III group B Streptococcus (OBS). Both preparations contained similar amounts of total IgO and specific IgO antibody against the type-specific polysaccharide. In vitro, opsonophagocytic studies revealed that pH 4-treated iv immunoglobulin was significantly more effective than reduced-andalkylated iv immunoglobulin in supporting neutrophil-mediated killing of the type III OBS strain. In vivo, both preparations resulted in similar levelsof serum antibody in newborn rats, but pH 4-treated iv immunoglobulin was signficantly more protective against the type III OBS strain. This was demonstrated by the lower magnitude of bacteremia, improved survival, and lower protective dose (PD50) in recipients of pH 4-treated iv immunoglobulin. Thus, reduced-and-alkylated iv immunoglobulin was less effective in vitro and in vivo against the strain of type III GBS than was pH 4-treated iv immunoglobulin. Further studies are needed to elucidate the mechanisms for this apparent discrepancy in functional activities of iv immunoglobulin.This publication has 4 references indexed in Scilit:
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- Deficiency of IgG Subclasses in Mothers of Infants with Group B Streptococcal SepticemiaInternational Archives of Allergy and Immunology, 1983
- Expression of biological effector functions by immunoglobulin G molecules lacking the hinge region.Proceedings of the National Academy of Sciences, 1981
- Correlation between Serum IgG-2 Concentrations and the Antibody Response to Bacterial Polysaccharide AntigensNew England Journal of Medicine, 1980