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Analysis of successful immune responses in persons infected with hepatitis C virus
被引:1064
作者:
Lechner, F
Wong, DKH
Dunbar, PR
Chapman, R
Chung, RT
Dohrenwend, P
Robbins, G
Phillips, R
Klenerman, P
Walker, BD
机构:
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Clin Med, Oxford OX3 9DU, England
[2] Univ Oxford, John Radcliffe Hosp, MRC, Human Immunol Unit, Oxford OX3 9DU, England
[3] Massachusetts Gen Hosp, Gastrointestinal Unit, Boston, MA 02129 USA
[4] Massachusetts Gen Hosp, Infect Dis Unit, Boston, MA 02129 USA
[5] Massachusetts Gen Hosp, AIDS Res Ctr, Boston, MA 02129 USA
[6] Harvard Univ, Sch Med, Boston, MA 02129 USA
基金:
英国惠康基金;
关键词:
acute infection;
cytotoxic T lymphocytes;
T helper cells;
tetramer staining;
interferon gamma;
D O I:
10.1084/jem.191.9.1499
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Although hepatitis C virus (HCV) infection is very common, identification of patients during acute infection is rare. Consequently, little is known about the immune response during this critical stage of the disease. We analyzed the T lymphocyte response during and after acute resolving HCV infection in three persons, using interferon (IFN)-gamma enzyme-linked immunospot (ELISPOT) and human histocompatibility leukocyte antigen (HLA) peptide tetramer assays. Acute infection was associated with a broadly directed T helper and cytotoxic T lymphocyte (CTL) response, which persisted after resolution of clinical hepatitis and clearance of viremia. At the earliest time point studied, highly activated CTL populations were observed that temporarily failed to secrete IFN-gamma, a "stunned" phenotype, from which they recovered as viremia declined, in long-term HCV-seropositive persons, CTL responses were more common in persons who had cleared viremia compared with those with persistent viremia, although the frequencies of HCV-specific CTLs were lower than those found in persons during and after resolution of acute HCV infection. These studies demonstrate a strong and persistent CTL response in resolving acute HCV infection, and provide rationale to explore immune augmentation as a therapeutic intervention in chronic HCV infection.
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页码:1499 / 1512
页数:14
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