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J. K. Sandberg, N. M. Fast, E. H. Palacios, G. Fennelly, J. Dobroszycki, P. Palumbo, et al., “Selective Loss of Innate CD4(+) V Alpha 24 Natural Killer T cells in Human Immunodeficiency Virus Infection,” Journal of Virology, Vol. 76, No. 15, 2002, pp. 7528-7534. doi:10.1128/JVI.76.15.7528-7534.2002

has been cited by the following article:

• TITLE: Greater Expansion of IFN-γ﹣ CD4+ NKT Cells in HIV-1 Compared with HIV-2-Infected Subjects with Preserved CD4+ T Cell Counts

  AUTHORS: Samuel V. Nuvor, Hilton Whittle, Sarah Rowland-Jones, Assan Jaye

  KEYWORDS: NKT Cells; HIV-1; HIV-2; IFN-g; CD4 T Cells

  JOURNAL NAME: World Journal of AIDS, Vol.2 No.2, June 15, 2012

  ABSTRACT: Context: Human Natural Killer T cells are T lymphocytes that express an invariant αβ T cells receptors and NK cells receptors. They regulate innate and adaptive immune response but are susceptible to HIV-1 infection. Objective: We compare the frequency and the activity of NKT cells in HIV-1 and HIV-2 infected individuals with CD4+ counts greater than 500/mm3 using flow cytometry after overnight stimulation with phytohemagglutinin (PHA). Results: The frequency of NKT cells was similar between both groups and also to sero-negative control subjects. There were also no significant differences in the proportions of total NKT cells and the CD4+ NKT subset that secreted interferon gamma (IFN-γ) after polyclonal stimulation. However, there was a significantly higher frequency of IFN-γ﹣ CD4+ NKT cells in HIV-1-infected compared with HIV-2 infected subjects (p = 0.043). Conclusion: These data suggest there is no relationship between the functional activity of NKT cell subsets and the total NKT cell population in HIV infection. The expansion of IFN-γ﹣ CD4+ NKT cells in HIV-1 infection may serve as target for viral infection and may eventually result in their depletion during chronic infection.