Hepatitis C virus variants circumventing cytotoxic T lymphocyte activity as a mechanism of chronicity
SL Tsai, YM Chen, MH Chen, CY Huang, IS Sheen… - Gastroenterology, 1998 - Elsevier
SL Tsai, YM Chen, MH Chen, CY Huang, IS Sheen, CT Yeh, JH Huang, GC Kuo, YF Liaw
Gastroenterology, 1998•ElsevierBackground & Aims: High rate of chronicity after acute hepatitis C virus (HCV) infection
cannot be explained in the presence of a multispecific cytotoxic T lymphocyte (CTL)
response. The aim of this study was to investigate the effect of virus variants on CTL activity
in patients in whom chronicity developed. Methods: CTL clones specific to a decapeptide
epitope derived from hypervariable region 1 were generated from 5 HLA-A2–positive
patients with acute hepatitis C by in vitro stimulation with synthetic peptides. The sequential …
cannot be explained in the presence of a multispecific cytotoxic T lymphocyte (CTL)
response. The aim of this study was to investigate the effect of virus variants on CTL activity
in patients in whom chronicity developed. Methods: CTL clones specific to a decapeptide
epitope derived from hypervariable region 1 were generated from 5 HLA-A2–positive
patients with acute hepatitis C by in vitro stimulation with synthetic peptides. The sequential …
Background & Aims
High rate of chronicity after acute hepatitis C virus (HCV) infection cannot be explained in the presence of a multispecific cytotoxic T lymphocyte (CTL) response. The aim of this study was to investigate the effect of virus variants on CTL activity in patients in whom chronicity developed.
Methods
CTL clones specific to a decapeptide epitope derived from hypervariable region 1 were generated from 5 HLA-A2–positive patients with acute hepatitis C by in vitro stimulation with synthetic peptides. The sequential change of this CTL epitope and its influence on the CTL recognition were examined.
Results
Virus variants did not appear in 3 patients with recovery, whereas variants with altered peptide ligands capable of antagonizing CTL activity emerged rapidly in the remaining 2 patients in whom chronicity developed. Importantly, these HLA-A2–restricted, hypervariable region 1–specific CTL clones shared the use of T-cell receptor (TCR) genes AV6 and BV17.
Conclusions
These data suggest that there is only a narrow T-cell repertoire responding to a single viral peptide/HLA ligand. The emergence of HCV variants with altered peptide ligands as TCR antagonists accompanied by a limited TCR repertoire may provide a mechanism for HCV chronicity. GASTROENTEROLOGY 1998;115:954-966
Elsevier