Quantitative Determination of Immunoglobulin G Specific for Group B Streptococcal β C Protein in Human Maternal Serum
Author(s) -
Catherine S. Lachenauer,
Carol J. Baker,
Miriam J. Baron,
Dennis L. Kasper,
Claudia Gravekamp,
Lawrence C. Madoff
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/338773
Subject(s) - antibody , group b , group a , epitope , immunoglobulin g , immunology , biology , beta (programming language) , streptococcus , medicine , bacteria , genetics , computer science , programming language
The beta C protein of group B streptococci (GBS) elicits antibody that is protective against GBS challenge in animals and is considered to be a potential component of a GBS conjugate vaccine. We developed a quantitative enzyme-linked immunosorbent assay to measure beta-specific serum immunoglobulin G (IgG) levels and used it to compare beta-specific IgG in a group of mothers of neonates with invasive type Ib/beta GBS disease and a group of mothers colonized with Ib/beta strains whose neonates remained well. beta-Specific IgG concentrations from these 2 groups were similar. To investigate differences in beta-specific antibody in animals and humans, protein fragments were generated that corresponded to major regions within the beta C protein. A single major region was predominantly recognized in human and rabbit serum samples. Thus, in contrast to immunized animals, no relationship was seen between levels of naturally acquired human beta-specific IgG and protection from neonatal disease. This difference was not explained by a major difference in epitope specificity.
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