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Theraputic Potential of Human Antisera to Group B Streptococcal Glycoconjugate Vaccines in Neonatal Mice
Author(s) -
Lawrence C. Paoletti,
Julieanne Pinel,
A K Rodewald,
Dennis L. Kasper
Publication year - 1997
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 - 10.1086/593678
Subject(s) - antiserum , toxoid , antibody , group b , immunization , conjugate vaccine , immunology , streptococcus , group a , microbiology and biotechnology , immunoglobulin g , glycoconjugate , tetanus , biology , medicine , vaccination , bacteria , bioinformatics , genetics
Experimental immunoglobulin preparations for treatment of group B streptococcal (GBS) infections contain low levels of functional antibody and exhibit lot-to-lot variability. GBS capsular polysaccharide-protein conjugate vaccines have recently been shown to produce high serum levels of type-specific antibody in healthy volunteers. Treatment of neonatal mice 4 h after inoculation with an ordinarily lethal dose of GBS type Ia, Ib, or III with pooled human serum from adults who had received GBS type Ia capsular polysaccharide-tetanus toxoid vaccine (Ia CPS-TT), Ib CPS-TT, or III CPS-TT resulted in 63%, 70%, and 75% survival, respectively. In contrast, < or = 17% of the infected mice treated with normal human serum or saline survived. These results demonstrate the therapeutic activity of GBS polysaccharide conjugate vaccine-induced antiserum and provide a rationale for the use of these vaccines in producing a functional, high-titered intravenous immunoglobulin preparation for clinical use.

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