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...
Saved in:
Published in | European journal of immunology Vol. 38; no. 2; pp. 350 - 363 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY‐VCH Verlag
01.02.2008
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
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. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0014-2980 1521-4141 |
DOI: | 10.1002/eji.200737768 |