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Hepatitis C virus-specific CD8+ T cell frequencies are associated with the responses of pegylated interferon-(alpha) and ribavirin combination therapy in patients with chronic hepatitis C virus infection (from Hepatology Research 2011, 41, 30-38)
Bibliografi
Author:
Tatsumi, Tomohide
;
Takehara, Tetsuo
;
Miyagi, Takuya
;
Nakazuru, Shoichi
;
Mita, Eiji
;
Kanto, Tatsuya
;
Hiramatsu, Naoki
;
Hayashi, Norio
Topik:
Chronic hepatitis C
;
HCV-specific CTL
;
IFN-g ELISPOT
;
Peg-IFNa
;
Ribavirin
;
Validation ref - 6
Bahasa:
(EN )
Penerbit:
The Japan Society of Hepatology
Tahun Terbit:
2011
Jenis:
Article - diterbitkan di jurnal ilmiah internasional
Fulltext:
tatsumi2010.pdf
(582.04KB;
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)
Abstract
Aim: Hepatitis C virus (HCV)-specific cytotoxic T lymphocytes (CTLs) play critical roles in elimination of the HCV-infected hepatocytes. However, the mechanism of HCV elimination by pegylated interferon-a (peg-IFNa) plus ribavirin is not fully understood. We examined HCV-specific CTL responses during this combination therapy.
Methods: CD8+ T cells were isolated from 16 HCV infected patients treated by this combination therapy and were subjected to IFN-g enzyme-linked immunospot (ELISPOT) assay.
Results: The numbers of IFN-g spots against HCV Core or NS3 protein-derived peptides in HCV patients before treatment were similar to those in healthy donors, and those in HCV patients significantly increased 4 weeks after the initiation of combination therapy. All HCV Core or NS3 proteins-derived peptides specific CD8+ T cells responses in pre-treated patients were not associated with ALT levels and HCV viral loads of HCV patients before treatment. And those in pre-treated patients were similar between sustained virologic responder (SVR) patients and non-SVR patients. Significant increase of HCV Core or NS3 proteins-derived peptides specific CD8+ T cells responses between before and 4 weeks after this combination therapy were observed in SVR patients, but not in non-SVR patients.
Conclusions: These results demonstrated that significant increase of HCV-specific CD8+ T cells at 4 weeks after the initiation of IFN treatment might be associated with the elimination of HCV. Our findings suggest that the reactivity against HCV Core and NS3 proteins-derived peptides might be useful in predicting the clinical outcome of the combination therapy of peg-IFNa and ribavirin.
[validation ref - 6]
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