Memory-like HCV-specific CD8+ T cells retain a molecular scar after cure of chronic HCV infection

被引:114
作者
Hensel, Nina [1 ,2 ,3 ]
Gu, Zuguang [4 ]
Sagar [1 ,5 ]
Wieland, Dominik [1 ,2 ]
Jechow, Katharina [6 ,7 ]
Kemming, Janine [1 ,2 ,3 ]
Llewellyn-Lacey, Sian [8 ]
Gosticle, Emma [8 ]
Sogukpinar, Oezlem [1 ,2 ]
Emmerich, Florian [2 ,9 ]
Price, David A. [8 ,10 ]
Bengsch, Bertram [1 ,2 ,11 ]
Boettler, Tobias [1 ,2 ]
Neumann-Haefelin, Christoph [1 ,2 ]
Eils, Roland [6 ,7 ,12 ]
Conrad, Christian [6 ,7 ]
Bartenschlager, Ralf [13 ,14 ,15 ]
Gruen, Dominic [5 ,11 ]
Ishaque, Naveed [6 ,7 ]
Thimme, Robert [1 ,2 ]
Hofmann, Maike [1 ,2 ]
机构
[1] Univ Hosp Freiburg, Dept Med 2, Freiburg, Germany
[2] Univ Freiburg, Fac Med, Freiburg, Germany
[3] Univ Freiburg, Fac Biol, Freiburg, Germany
[4] German Canc Res Ctr, Heidelberg Ctr Personalised Oncol DKFZ HIPO, Heidelberg, Germany
[5] Max Planck Inst Immunobiol & Epigenet, Freiburg, Germany
[6] Charite Univ Med Berlin, Berlin, Germany
[7] Berlin Inst Hlth, Digital Hlth Ctr, Berlin, Germany
[8] Cardiff Univ, Div Infect & Immun, Sch Med, Cardiff, Wales
[9] Univ Freiburg, Univ Med Ctr, Inst Transfus Med & Gene Therapy, Freiburg, Germany
[10] Cardiff Univ, Syst Immun Res Inst, Sch Med, Cardiff, Wales
[11] Univ Freiburg, Signalling Res Ctr BIOSS & CIBSS, Freiburg, Germany
[12] Heidelberg Univ, Fac Med, Hlth Data Sci Unit, Heidelberg, Germany
[13] Heidelberg Univ, Dept Infect Dis, Mol Virol, Heidelberg, Germany
[14] German Canc Res Ctr, Div Virus Associated Carcinogenesis, Heidelberg, Germany
[15] German Ctr Infect Res DZIF, Partner Site Heidelberg, Heidelberg, Germany
基金
英国惠康基金;
关键词
VIRUS PERSISTENCE; PD-1; EXPRESSION; EXHAUSTION; DIFFERENTIATION; DYSFUNCTION; RESTORATION; ALIGNMENT; SUBSETS;
D O I
10.1038/s41590-020-00817-w
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In chronic hepatitis C virus (HCV) infection, exhausted HCV-specific CD8(+) T cells comprise memory-like and terminally exhausted subsets. However, little is known about the molecular profile and fate of these two subsets after the elimination of chronic antigen stimulation by direct-acting antiviral (DAA) therapy. Here, we report a progenitor-progeny relationship between memory-like and terminally exhausted HCV-specific CD8(+) T cells via an intermediate subset. Single-cell transcriptomics implicated that memory-like cells are maintained and terminally exhausted cells are lost after DAA-mediated cure, resulting in a memory polarization of the overall HCV-specific CD8(+) T cell response. However, an exhausted core signature of memory-like CD8(+) T cells was still detectable, including, to a smaller extent, in HCV-specific CD8(+) T cells targeting variant epitopes. These results identify a molecular signature of T cell exhaustion that is maintained as a chronic scar in HCV-specific CD8(+) T cells even after the cessation of chronic antigen stimulation. Thimme and colleagues identify a molecular signature of T cell exhaustion resembling a 'chronic scar' that is imprinted in hepatitis C virus-specific CD8(+) T cells and cannot simply be reversed by viral clearance.
引用
收藏
页码:229 / U246
页数:27
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