细胞毒性T细胞
CD8型
免疫学
丙型肝炎病毒
生物
T细胞
病毒学
抗原
病毒
慢性感染
免疫系统
生物化学
体外
作者
Nina Hensel,Zuguang Gu,Sagar Sagar,Dominik Wieland,Katharina Jechow,Janine Kemming,Sian Llewellyn‐Lacey,Emma Gostick,Oezlem Sogukpinar,Florian Emmerich,David A. Price,Bertram Bengsch,Tobias Boettler,Christoph Neumann–Haefelin,Roland Eils,Christian Conrad,Ralf Bartenschlager,Dominic Grün,Naveed Ishaque,Robert Thimme,Maike Hofmann
标识
DOI:10.1038/s41590-020-00817-w
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.
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