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Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19
Author(s) -
Jason Neidleman,
Xiaoyu Luo,
Ashley F. George,
Matthew McGregor,
Junkai Yang,
Cassandra Yun,
Victoria Murray,
Gurjot Gill,
Warner C. Greene,
Joshua Vasquez,
Sulggi A. Lee,
Eliver Ghosn,
Kara L. Lynch,
Nadia R. Roan
Publication year - 2021
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2021.109414
Subject(s) - immunology , covid-19 , coronavirus , pathogenesis , homing (biology) , biology , bystander effect , t cell , medicine , virology , immune system , disease , pathology , infectious disease (medical specialty) , ecology
Although T cells are likely players in SARS-CoV-2 immunity, little is known about the phenotypic features of SARS-CoV-2-specific T cells associated with recovery from severe COVID-19. We analyze T cells from 34 COVID-19 patients with severities ranging from mild (outpatient) to critical culminating in death. Relative to patients that succumbed, individuals that recovered from severe COVID-19 harbor elevated and increasing numbers of SARS-CoV-2-specific T cells capable of homeostatic proliferation. In contrast, fatal COVID-19 displays elevated numbers of SARS-CoV-2-specific regulatory T cells and a time-dependent escalation in activated bystander CXCR4+ T cells as assessed by longitudinal sampling. Together with the demonstration of increased proportions of inflammatory CXCR4+ T cells in the lungs of severe COVID-19 patients, these results support a model whereby lung-homing T cells activated through bystander effects contribute to immunopathology, while a robust, non-suppressive SARS-CoV-2-specific T cell response limits pathogenesis and promotes recovery from severe COVID-19.

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