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10.1172/jci.insight.151571

http://scihub22266oqcxt.onion/10.1172/jci.insight.151571
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suck abstract from ncbi


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pmid34283810      JCI+Insight 2021 ; 6 (18): ä
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  • CD8+PD-L1+CXCR3+ polyfunctional T cell abundances are associated with survival in critical SARS-CoV-2-infected patients #MMPMID34283810
  • Adam L; Rosenbaum P; Quentric P; Parizot C; Bonduelle O; Guillou N; Corneau A; Dorgham K; Miyara M; Luyt CE; Guihot A; Gorochov G; Combadiere C; Combadiere B
  • JCI Insight 2021[Sep]; 6 (18): ä PMID34283810show ga
  • The importance of the adaptive T cell response in the control and resolution of viral infection has been well established. However, the nature of T cell-mediated viral control mechanisms in life-threatening stages of COVID-19 has yet to be determined. The aim of the present study was to determine the function and phenotype of T cell populations associated with survival or death of patients with COVID-19 in intensive care as a result of phenotypic and functional profiling by mass cytometry. Increased frequencies of circulating, polyfunctional CD4+CXCR5+HLA-DR+ stem cell memory T cells (Tscms) and decreased proportions of granzyme B-expressing and perforin-expressing effector memory T cells were detected in recovered and deceased patients, respectively. The higher abundance of polyfunctional PD-L1+CXCR3+CD8+ effector T cells (Teffs), CXCR5+HLA-DR+ Tscms, and anti-nucleocapsid (anti-NC) cytokine-producing T cells permitted us to differentiate between recovered and deceased patients. The results from a principal component analysis show an imbalance in the T cell compartment that allowed for the separation of recovered and deceased patients. The paucity of circulating PD-L1+CXCR3+CD8+ Teffs and NC-specific CD8+ T cells accurately forecasts fatal disease outcome. This study provides insight into the nature of the T cell populations involved in the control of COVID-19 and therefore might impact T cell-based vaccine designs for this infectious disease.
  • |*Immunity, Cellular[MESH]
  • |Adult[MESH]
  • |B7-H1 Antigen/*immunology[MESH]
  • |CD4-Positive T-Lymphocytes/*immunology[MESH]
  • |CD8 Antigens/*immunology[MESH]
  • |CD8-Positive T-Lymphocytes/*immunology[MESH]
  • |COVID-19/*immunology/mortality/pathology[MESH]
  • |Epitopes, T-Lymphocyte/immunology[MESH]
  • |Female[MESH]
  • |France/epidemiology[MESH]
  • |Humans[MESH]
  • |Immunologic Memory[MESH]
  • |Lymphocyte Activation[MESH]
  • |Male[MESH]
  • |Receptors, CXCR3/*immunology[MESH]
  • |SARS-CoV-2[MESH]


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