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10.1126/sciimmunol.abe4782

http://scihub22266oqcxt.onion/10.1126/sciimmunol.abe4782
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33478949!8101257!33478949
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suck abstract from ncbi


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pmid33478949      Sci+Immunol 2021 ; 6 (55): ä
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  • Severely ill COVID-19 patients display impaired exhaustion features in SARS-CoV-2-reactive CD8(+) T cells #MMPMID33478949
  • Kusnadi A; Ramirez-Suastegui C; Fajardo V; Chee SJ; Meckiff BJ; Simon H; Pelosi E; Seumois G; Ay F; Vijayanand P; Ottensmeier CH
  • Sci Immunol 2021[Jan]; 6 (55): ä PMID33478949show ga
  • The molecular properties of CD8(+) T cells that respond to SARS-CoV-2 infection are not fully known. Here, we report on the single-cell transcriptomes of >80,000 virus-reactive CD8(+) T cells, obtained using a modified Antigen-Reactive T cell Enrichment (ARTE) assay, from 39 COVID-19 patients and 10 healthy subjects. COVID-19 patients segregated into two groups based on whether the dominant CD8(+) T cell response to SARS-CoV-2 was 'exhausted' or not. SARS-CoV-2-reactive cells in the exhausted subset were increased in frequency and displayed lesser cytotoxicity and inflammatory features in COVID-19 patients with mild compared to severe illness. In contrast, SARS-CoV-2-reactive cells in the dominant non-exhausted subset from patients with severe disease showed enrichment of transcripts linked to co-stimulation, pro-survival NF-kappaB signaling, and anti-apoptotic pathways, suggesting the generation of robust CD8(+) T cell memory responses in patients with severe COVID-19 illness. CD8(+) T cells reactive to influenza and respiratory syncytial virus from healthy subjects displayed polyfunctional features and enhanced glycolysis. Cells with such features were largely absent in SARS-CoV-2-reactive cells from both COVID-19 patients and healthy controls non-exposed to SARS-CoV-2. Overall, our single-cell analysis revealed substantial diversity in the nature of CD8(+) T cells responding to SARS-CoV-2.
  • |Adult[MESH]
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |CD8-Positive T-Lymphocytes/*immunology[MESH]
  • |COVID-19/*immunology[MESH]
  • |Female[MESH]
  • |Glycolysis/immunology[MESH]
  • |Humans[MESH]
  • |Immunologic Memory/immunology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |NF-kappa B/immunology[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Signal Transduction/immunology[MESH]
  • |Single-Cell Analysis/methods[MESH]


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