In:
Journal of Virology, American Society for Microbiology, Vol. 79, No. 12 ( 2005-06-15), p. 7860-7867
Abstract:
Chronic hepatitis C virus (HCV) infection is associated with impaired proliferative, cytokine, and cytotoxic effector functions of HCV-specific CD8 + T cells that probably contribute significantly to viral persistence. Here, we investigated the potential role of T cells with a CD4 + CD25 + regulatory phenotype in suppressing virus-specific CD8 + T-cell proliferation during chronic HCV infection. In vitro depletion studies and coculture experiments revealed that peptide specific proliferation as well as gamma interferon production of HCV-specific CD8 + T cells were inhibited by CD4 + CD25 + T cells. This inhibition was dose dependent, required direct cell-cell contact, and was independent of interleukin-10 and transforming growth factor beta. Interestingly, the T-cell-mediated suppression in chronically HCV-infected patients was not restricted to HCV-specific CD8 + T cells but also to influenza virus-specific CD8 + T cells. Importantly, CD4 + CD25 + T cells from persons recovered from HCV infection and from healthy blood donors exhibited significantly less suppressor activity. Thus, the inhibition of virus-specific CD8 + T-cell proliferation was enhanced in chronically HCV-infected patients. This was associated with a higher frequency of circulating CD4 + CD25 + cells observed in this patient group. Taken together, our results suggest that chronic HCV infection leads to the expansion of CD4 + CD25 + T cells that are able to suppress CD8 + T-cell responses to different viral antigens. Our results further suggest that CD4 + CD25 + T cells may contribute to viral persistence in chronically HCV-infected patients and may be a target for immunotherapy of chronic hepatitis C.
Type of Medium:
Online Resource
ISSN:
0022-538X
,
1098-5514
DOI:
10.1128/JVI.79.12.7860-7867.2005
Language:
English
Publisher:
American Society for Microbiology
Publication Date:
2005
detail.hit.zdb_id:
1495529-5
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