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10.1016/j.celrep.2021.109414

http://scihub22266oqcxt.onion/10.1016/j.celrep.2021.109414
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suck abstract from ncbi


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pmid34260965      Cell+Rep 2021 ; 36 (3): 109414
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  • Distinctive features of SARS-CoV-2-specific T cells predict recovery from severe COVID-19 #MMPMID34260965
  • Neidleman J; Luo X; George AF; McGregor M; Yang J; Yun C; Murray V; Gill G; Greene WC; Vasquez J; Lee SA; Ghosn E; Lynch KL; Roan NR
  • Cell Rep 2021[Jul]; 36 (3): 109414 PMID34260965show ga
  • Although T cells are likely players in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) immunity, little is known about the phenotypic features of SARS-CoV-2-specific T cells associated with recovery from severe coronavirus disease 2019 (COVID-19). We analyze T cells from 34 individuals with COVID-19 with severity ranging from mild (outpatient) to critical, culminating in death. Relative to individuals who succumbed, individuals who 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 cases display 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 individuals with severe COVID-19, these results support a model where lung-homing T cells activated through bystander effects contribute to immunopathology, whereas a robust, non-suppressive SARS-CoV-2-specific T cell response limits pathogenesis and promotes recovery from severe COVID-19.
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