CD4 T Helper Type 1 and Regulatory T Cells Induced against the Same Epitopes on the Core Protein in Hepatitis C Virus-Infected Persons
The factors that determine persistence or clearance of hepatitis C virus (HCV) infection are poorly understood. The CD4 T cell responses to the HCV core protein were examined in a cohort of women infected with a single genotype of HCV. CD4 T cells from HCV-infected patients secreted interferon (IFN)...
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Published in | The Journal of infectious diseases Vol. 185; no. 6; pp. 720 - 727 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chicago, IL
The University of Chicago Press
15.03.2002
University of Chicago Press Oxford University Press |
Subjects | |
Online Access | Get full text |
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Summary: | The factors that determine persistence or clearance of hepatitis C virus (HCV) infection are poorly understood. The CD4 T cell responses to the HCV core protein were examined in a cohort of women infected with a single genotype of HCV. CD4 T cells from HCV-infected patients secreted interferon (IFN)-γ in response to peptides from 4 immunodominant regions of the core protein, and these responses were stronger in persistently infected women. Interleukin (IL)-10 was also produced by CD4 T cells from HCV-infected subjects in response to the same core peptides. Furthermore, HCV core-specific CD4 T cell clones secreted either IFN-γ or IL-10 but not IL-4. These findings demonstrate that T helper type 1 and regulatory T cells are induced against the same epitopes on the core protein during HCV infection. |
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Bibliography: | ark:/67375/HXZ-RNBNGHK0-S Present affiliations: Molecular Parasitology, New York Blood Center, New York (A.J.M.); Liver Center, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, Massachusetts (M.C.). istex:2038727B57E0978197631B60D8973BC58F86B0F4 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
ISSN: | 0022-1899 1573-6613 1537-6613 |
DOI: | 10.1086/339340 |