Differentiation and fate of virus-specific CD8(+) T cells after cessation of chronic antigen stimulation is unclear. Here we show that a TCF1(+)CD127(+)PD1(+) hepatitis C virus (HCV)-specific CD8(+) T-cell subset exists in chronically infected patients with phenotypic features of T-cell exhaustion and memory, both before and after treatment with direct acting antiviral (DAA) agents. This subset is maintained during, and for a long duration after, HCV elimination. After antigen re-challenge the less differentiated TCF1(+)CD127(+)PD1(+) population expands, which is accompanied by emergence of terminally exhausted TCF1-CD127-PD1(hi) HCV-specific CD8(+) T cells. These results suggest the TCF1(+)CD127(+)PD1(+) HCV-specific CD8(+) T-cell subset has memory-like characteristics, including antigen-independent survival and recall proliferation. We thus provide evidence for the establishment of memory-like virus-specific CD8(+) T cells in a clinically relevant setting of chronic viral infection and we uncover their fate after cessation of chronic antigen stimulation, implicating a potential strategy for antiviral immunotherapy.
TCF1(+) hepatitis C virus-specific CD8(+) T cells are maintained after cessation of chronic antigen stimulation.
慢性抗原刺激停止后,TCF1(+)丙型肝炎病毒特异性CD8(+)T细胞得以维持
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作者:Wieland Dominik, Kemming Janine, Schuch Anita, Emmerich Florian, Knolle Percy, Neumann-Haefelin Christoph, Held Werner, Zehn Dietmar, Hofmann Maike, Thimme Robert
| 期刊: | Nature Communications | 影响因子: | 15.700 |
| 时间: | 2017 | 起止号: | 2017 May 3; 8:15050 |
| doi: | 10.1038/ncomms15050 | 靶点: | CD8 |
| 研究方向: | 细胞生物学 | ||
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