Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/43410
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dc.contributor.authorZhang, Q.en
dc.contributor.authorBagrade, L.en
dc.contributor.authorBernatoniene, J.en
dc.contributor.authorClarke, E.en
dc.contributor.authorPaton, J.en
dc.contributor.authorMitchell, T.en
dc.contributor.authorNunez, D.en
dc.contributor.authorFinn, A.en
dc.date.issued2007en
dc.identifier.citationJournal of Infectious Diseases, 2007; 195(8):1194-1202en
dc.identifier.issn0022-1899en
dc.identifier.issn1537-6613en
dc.identifier.urihttp://hdl.handle.net/2440/43410-
dc.description© 2007 by the Infectious Diseases Society of America. All rights reserved.en
dc.description.abstract<h4>Background</h4>Recent studies in mice have suggested that T cell immunity may be protective against pneumococcal infection.<h4>Methods</h4>CD4 T cell proliferative responses to the pneumococcal proteins pneumolysin (Ply), Ply toxoid (F433), and choline-binding protein A were investigated in peripheral blood mononuclear cells (PBMCs) and adenoidal mononuclear cells (MNCs) obtained from children undergoing adenoidectomy.<h4>Results</h4>Ply and F433 induce significant proliferation of CD4 T cells in both PBMCs and adenoidal MNCs, and both memory and naive phenotypes of CD4 T cells proliferated after stimulation. In PBMCs, CD4 T cell proliferation induced by Ply and F433, which was associated with increased production of interferon (IFN)- gamma and tumor necrosis factor (TNF)- alpha , was significantly lower in children who were culture positive for pneumococcus than in those who were culture negative for pneumococcus (P<.05). Between groups, no such difference was observed in adenoidal MNC CD4 T cell proliferation, which was associated with production of IFN- gamma and interleukin (IL)-10. The CD4 T cell proliferation induced by Ply and F433 was inhibited by antibodies to Toll-like receptor 4.<h4>Conclusion</h4>These data suggest that Ply induces CD4 T cell proliferative responses with production of IFN- gamma and TNF- alpha in PBMCs or of IFN- gamma and IL-10 in adenoidal MNCs, which may be important in modulating pneumococcal carriage in children.en
dc.description.statementofresponsibilityQibo Zhang, Linda Bagrade, Jolanta Bernatoniene, Ed Clarke, James C. Paton, Tim J. Mitchell, Desmond A. Nunez, and Adam Finnen
dc.language.isoenen
dc.publisherUniv Chicago Pressen
dc.source.urihttp://www.journals.uchicago.edu/doi/abs/10.1086/512617en
dc.subjectNasopharynx; CD4-Positive T-Lymphocytes; Cells, Cultured; Humans; Streptococcus pneumoniae; Pneumococcal Infections; Tumor Necrosis Factor-alpha; Bacterial Proteins; Streptolysins; Antibodies, Bacterial; Carrier State; Cell Proliferation; Time Factors; Child; Child, Preschool; Female; Male; Toll-Like Receptors; Interferon-gammaen
dc.titleLow CD4 T cell immunity to pneumolysin is associated with nasopharyngeal carriage of pneumococci in childrenen
dc.typeJournal articleen
dc.identifier.doi10.1086/512617en
pubs.publication-statusPublisheden
dc.identifier.orcidPaton, J. [0000-0001-9807-5278]en
Appears in Collections:Molecular and Biomedical Science publications

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