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10.1016/j.ymthe.2020.10.001

http://scihub22266oqcxt.onion/10.1016/j.ymthe.2020.10.001
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33186542!7543694!33186542
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suck abstract from ncbi


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pmid33186542      Mol+Ther 2020 ; 28 (12): 2691-2702
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  • COVID-19-Induced ARDS Is Associated with Decreased Frequency of Activated Memory/Effector T Cells Expressing CD11a(+) #MMPMID33186542
  • Anft M; Paniskaki K; Blazquez-Navarro A; Doevelaar A; Seibert FS; Holzer B; Skrzypczyk S; Kohut E; Kurek J; Zapka J; Wehler P; Kaliszczyk S; Bajda S; Thieme CJ; Roch T; Konik MJ; Berger MM; Brenner T; Kolsch U; Meister TL; Pfaender S; Steinmann E; Tempfer C; Watzl C; Dolff S; Dittmer U; Abou-El-Enein M; Westhoff TH; Witzke O; Stervbo U; Babel N
  • Mol Ther 2020[Dec]; 28 (12): 2691-2702 PMID33186542show ga
  • Preventing the progression to acute respiratory distress syndrome (ARDS) in COVID-19 is an unsolved challenge. The involvement of T cell immunity in this exacerbation remains unclear. To identify predictive markers of COVID-19 progress and outcome, we analyzed peripheral blood of 10 COVID-19-associated ARDS patients and 35 mild/moderate COVID-19 patients, not requiring intensive care. Using multi-parametric flow cytometry, we compared quantitative, phenotypic, and functional characteristics of circulating bulk immune cells, as well as SARS-CoV-2 S-protein-reactive T cells between the two groups. ARDS patients demonstrated significantly higher S-protein-reactive CD4(+) and CD8(+) T cells compared to non-ARDS patients. Of interest, comparison of circulating bulk T cells in ARDS patients to non-ARDS patients demonstrated decreased frequencies of CD4(+) and CD8(+) T cell subsets, with activated memory/effector T cells expressing tissue migration molecule CD11a(+)(+). Importantly, survival from ARDS (4/10) was accompanied by a recovery of the CD11a(+)(+) T cell subsets in peripheral blood. Conclusively, data on S-protein-reactive polyfunctional T cells indicate the ability of ARDS patients to generate antiviral protection. Furthermore, decreased frequencies of activated memory/effector T cells expressing tissue migratory molecule CD11a(+)(+) observed in circulation of ARDS patients might suggest their involvement in ARDS development and propose the CD11a-based immune signature as a possible prognostic marker.
  • |*Pandemics[MESH]
  • |Adult[MESH]
  • |Aged[MESH]
  • |CD4-Positive T-Lymphocytes/immunology[MESH]
  • |CD8-Positive T-Lymphocytes/immunology[MESH]
  • |COVID-19/*immunology/virology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunologic Memory/*immunology[MESH]
  • |Male[MESH]
  • |Membrane Glycoproteins/immunology[MESH]
  • |Middle Aged[MESH]
  • |Respiratory Distress Syndrome/*immunology/pathology/virology[MESH]
  • |SARS-CoV-2/immunology/pathogenicity[MESH]
  • |T-Lymphocyte Subsets/immunology[MESH]


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