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dc.contributor.authorJuno, Jennifer A
dc.contributor.authorLajoie, Julie
dc.contributor.authorStalker, Andrew T
dc.contributor.authorOyugi, Julius
dc.contributor.authorKimani, Makobu
dc.contributor.authorKimani, Joshua
dc.contributor.authorPlummer, Francis A
dc.contributor.authorFowke, Keith R
dc.date.accessioned2014-12-30T12:38:28Z
dc.date.available2014-12-30T12:38:28Z
dc.date.issued2014-12
dc.identifier.citationAmerican Journal of Reproductive Immunology Volume 72, Issue 6, pages 534–540, December 2014en_US
dc.identifier.urihttp://onlinelibrary.wiley.com/doi/10.1111/aji.12308/abstract?deniedAccessCustomisedMessage=&userIsAuthenticated=false
dc.identifier.urihttp://hdl.handle.net/11295/78591
dc.description.abstractProblem The expression of inhibitory markers such as LAG-3 and PD-1 on T lymphocytes regulates immune function. Their expression at the genital mucosa is poorly understood, but regulation of immune activation at the female genital tract likely controls susceptibility to sexually transmitted infections. Method of study Cervical mononuclear cells were phenotyped by flow cytometry. Concentrations of cytokines were determined in cervical-vaginal lavage samples by bead array. Results LAG-3 expression was significantly elevated at the genital mucosa and was associated with expression of CCR5 and CD69. Double negative (DN) T cells expressed the highest levels of LAG-3, but not PD-1, and were more activated than other T lymphocytes. Conclusion The elevated expression of LAG-3 at the genital tract suggests it may regulate T-cell activation, and identify cells susceptible to HIV infection. The enrichment of LAG-3 on DN T cells suggests LAG-3 may contribute to the immunoregulatory activity of these cells.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.subjectCervical; exhaustion; HIV ; LAG-3; sexually transmitted infectionen_US
dc.titleEnrichment of LAG-3, but not PD-1, on Double Negative T Cells at the Female Genital Tracten_US
dc.typeArticleen_US
dc.type.materialenen_US


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