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dc.contributor.authorCohen, C.R
dc.contributor.authorKoochesfahani, K.M
dc.contributor.authorMeier, A S
dc.contributor.authorShen, C
dc.contributor.authorKarunakaran, K
dc.contributor.authorOndondo, B
dc.contributor.authorKinyari, T
dc.contributor.authorMugo, N R
dc.contributor.authorNguti, R
dc.contributor.authorBrunham., R C
dc.date.accessioned2013-04-22T13:12:05Z
dc.date.available2013-04-22T13:12:05Z
dc.date.issued2005
dc.identifier.citationJ Infect Dis. 2005 Aug 15;192(4):591-9. Epub 2005 Jul 7en
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/16503
dc.description.abstractEpidemiological, animal, and in vitro investigations suggest that Chlamydia trachomatis infection engenders acquired immunity, the basis for which is incompletely defined, especially in humans. In a prospective cohort study of women at high risk for C. trachomatis infection, we found that, at baseline and after adjustment for age and other potential confounding variables, production of interferon- gamma by peripheral-blood mononuclear cells (PBMCs) stimulated with chlamydia heat-shock protein 60 strongly correlated with protection against incident C. trachomatis infection. This investigation supports a direct role for C. trachomatis-specific immune responses in altering the risk of infection and suggests immune correlates of protection that are potentially useful in vaccine development.en
dc.language.isoenen
dc.titleImmunoepidemiologic profile of Chlamydia trachomatis infection:Importance of Heat-Shock Protein 60 and Interferon-γen
dc.title.alternativeimportance of heat-shock protein 60 and interferon- gamma.en
dc.typeArticleen


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