Polyfunctional T cell responses are a hallmark of HIV‐2 infection

HIV‐2 is distinguished clinically and immunologically from HIV‐1 infection by delayed disease progression and maintenance of HIV‐specific CD4+ T cell help in most infected subjects. Thus, HIV‐2 provides a unique natural human model in which to investigate correlates of immune protection against HIV...

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Published inEuropean journal of immunology Vol. 38; no. 2; pp. 350 - 363
Main Authors Duvall, Melody G., Precopio, Melissa L., Ambrozak, David A., Jaye, Assan, McMichael, Andrew J., Whittle, Hilton C., Roederer, Mario, Rowland‐Jones, Sarah L., Koup, Richard A.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY‐VCH Verlag 01.02.2008
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Summary:HIV‐2 is distinguished clinically and immunologically from HIV‐1 infection by delayed disease progression and maintenance of HIV‐specific CD4+ T cell help in most infected subjects. Thus, HIV‐2 provides a unique natural human model in which to investigate correlates of immune protection against HIV disease progression. Here, we report a detailed assessment of the HIV‐2‐specific CD4+ and CD8+ T cell response compared to HIV‐1, using polychromatic flow cytometry to assess the quality of the HIV‐specific T cell response by measuring IFN‐γ, IL‐2, TNF‐α, MIP‐1β, and CD107a mobilization (degranulation) simultaneously following Gag peptide stimulation. We find that HIV‐2‐specific CD4+ and CD8+ T cells are more polyfunctional that those specific for HIV‐1 and that polyfunctional HIV‐2‐specific T cells produce more IFN‐γ and TNF‐α on a per‐cell basis than monofunctional T cells. Polyfunctional HIV‐2‐specific CD4+ T cells were generally more differentiated and expressed CD57, while there was no association between function and phenotype in the CD8+ T cell fraction. Polyfunctional HIV‐specific T cell responses are a hallmark of non‐progressive HIV‐2 infection and may be related to good clinical outcome in this setting.
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ISSN:0014-2980
1521-4141
DOI:10.1002/eji.200737768