| Literature DB >> 32846135 |
Ioana Sandu1, Dario Cerletti1, Nathalie Oetiker2, Mariana Borsa2, Franziska Wagen2, Ilaria Spadafora2, Suzanne P M Welten2, Ugne Stolz2, Annette Oxenius3, Manfred Claassen4.
Abstract
A hallmark of chronic infections is the presence of exhausted CD8 T cells, characterized by a distinct transcriptional program compared with functional effector or memory cells, co-expression of multiple inhibitory receptors, and impaired effector function, mainly driven by recurrent T cell receptor engagement. In the context of chronic lymphocytic choriomeningitis virus (LCMV) infection in mice, most studies focused on studying splenic virus-specific CD8 T cells. Here, we provide a detailed characterization of exhausted CD8 T cells isolated from six different tissues during established LCMV infection, using single-cell RNA sequencing. Our data reveal that exhausted cells are heterogeneous, adopt organ-specific transcriptomic profiles, and can be divided into five main functional subpopulations: advanced exhaustion, effector-like, intermediate, proliferating, or memory-like. Adoptive transfer experiments showed that these phenotypes are plastic, suggesting that the tissue microenvironment has a major impact in shaping the phenotype and function of virus-specific CD8 T cells during chronic infection.Entities:
Keywords: CD8 T cells; chronic viral infection; phenotypic plasticity; singe cell RNA sequencing; tissue-specific phenotypes
Mesh:
Year: 2020 PMID: 32846135 DOI: 10.1016/j.celrep.2020.108078
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423