Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/9585
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dc.contributor.authorNuvor, Samuel Victor-
dc.contributor.authorRowland-jones, Sarah-
dc.contributor.authorWhittle, Hilton-
dc.contributor.authorJaye, Assan-
dc.date.accessioned2023-10-17T16:41:32Z-
dc.date.available2023-10-17T16:41:32Z-
dc.date.issued2010-
dc.identifier.urihttp://hdl.handle.net/123456789/9585-
dc.description.abstractBackground The role of NK cells in slowing disease progression in HIV-2 infected individuals compare to HIV-1 infected individuals. Methods In this study peripheral blood mononuclear cells were obtained from 30 HIV-1 and 30 HIV-2 infected subjects from each of 3 categories of CD4 T-cell counts (>500, 200-500 and <200 cells/ul) together with 50 HIV uninfected control subjects. Lytic activity and IFN-g secretion by NK cells from HIV-1 and HIV-2 infected subjects were measured by chromium-release and ELISPOT assays respectively following incubation of PBMC with the NK-sensitive K562 cells. Viral load was also measured from the plasma samples of the subjects. Results The cytotoxic response by NK cells was significantly higher in HIV-2 than in HIV-1 infection in subjects with CD4-T cell count >500 cell/ul (p < 0.05) and was similar to that of the healthy controls. There was a significant correlation between the magnitude of the NK population and cytolytic activity in HIV-2 individuals (r = 0.27, p = 0.01). There was also an inverse relationship between the cytolytic activity and plasma viral load in HIV-2 infected subjects (r = -0.27, p = 0.009). Interferon-g secretion by NK cells in ELISPOT assays was similar in HIV-1 and HIV-2 infections at all categories of CD4+T cell counts.en_US
dc.language.isoenen_US
dc.publisherRetrovirologyen_US
dc.subjectCytotoxicen_US
dc.subjectInterferon-g secretionen_US
dc.subjectNatural Killer Cellsen_US
dc.subjectHIV-1en_US
dc.subjectHIV-2en_US
dc.subjectinfected individualsen_US
dc.titleComparison of Cytotoxic activity and Interferon-g secretion by Natural Killer Cells in HIV-1 and HIV-2 infected individualsen_US
dc.typeArticleen_US
Appears in Collections:School of Medical Sciences



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