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Effects of Group B Streptococci on Cord and Adult Mononuclear Cell Interleukin‐12 and Interferon‐γ mRNA Accumulation and Protein Secretion
Author(s) -
Joanna JoynerMatos,
Nancy H. Augustine,
Kristen A. Taylor,
Timothy R. La Pine,
Harry R. Hill
Publication year - 2000
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 - 10.1086/315796
Subject(s) - secretion , peripheral blood mononuclear cell , group a , interferon , microbiology and biotechnology , immunology , group b , interleukin , biology , messenger rna , interleukin 4 , cytokine , virology , medicine , endocrinology , gene , in vitro , biochemistry
Group B streptococci (GBS) are a major cause of early-onset infection in neonates. Neonates, who have defects in neutrophil function that likely contribute to susceptibility to GBS infection, are deficient in the production of the phagocyte activator interferon (IFN)-gamma. GBS-stimulated mRNA accumulation and protein secretion of IFN-gamma and interleukin (IL)-12, a major enhancer of IFN-gamma production, by mixed mononuclear cells (MMCs) from umbilical cord and adult peripheral blood was examined. GBS-exposed cord blood MMCs secreted lower concentrations of both IL-12 and IFN-gamma proteins than did MMCs from adults. IL-12 and IFN-gamma mRNA accumulation was examined by use of comparative reverse transcriptase-polymerase chain reaction. Cord blood MMCs accumulated less mRNA for both IL-12 and IFN-gamma than did adult blood MMC. The deficiency in cord blood cell production of IL-12 may have a role in inadequate IFN-gamma production, which contributes to the unique susceptibility of neonates to GBS infections.

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