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10.1016/j.ebiom.2020.102885

http://scihub22266oqcxt.onion/10.1016/j.ebiom.2020.102885
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32650275!7338277!32650275
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suck abstract from ncbi


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pmid32650275      EBioMedicine 2020 ; 57 (ä): 102885
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  • Reappearance of effector T cells is associated with recovery from COVID-19 #MMPMID32650275
  • Odak I; Barros-Martins J; Bosnjak B; Stahl K; David S; Wiesner O; Busch M; Hoeper MM; Pink I; Welte T; Cornberg M; Stoll M; Goudeva L; Blasczyk R; Ganser A; Prinz I; Forster R; Koenecke C; Schultze-Florey CR
  • EBioMedicine 2020[Jul]; 57 (ä): 102885 PMID32650275show ga
  • BACKGROUND: Elucidating the role of T cell responses in COVID-19 is of utmost importance to understand the clearance of SARS-CoV-2 infection. METHODS: 30 hospitalized COVID-19 patients and 60 age- and gender-matched healthy controls (HC) participated in this study. We used two comprehensive 11-colour flow cytometric panels conforming to Good Laboratory Practice and approved for clinical diagnostics. FINDINGS: Absolute numbers of lymphocyte subsets were differentially decreased in COVID-19 patients according to clinical severity. In severe disease (SD) patients, all lymphocyte subsets were reduced, whilst in mild disease (MD) NK, NKT and gammadelta T cells were at the level of HC. Additionally, we provide evidence of T cell activation in MD but not SD, when compared to HC. Follow up samples revealed a marked increase in effector T cells and memory subsets in convalescing but not in non-convalescing patients. INTERPRETATION: Our data suggest that activation and expansion of innate and adaptive lymphocytes play a major role in COVID-19. Additionally, recovery is associated with formation of T cell memory as suggested by the missing formation of effector and central memory T cells in SD but not in MD. Understanding T cell-responses in the context of clinical severity might serve as foundation to overcome the lack of effective anti-viral immune response in severely affected COVID-19 patients and can offer prognostic value as biomarker for disease outcome and control. FUNDING: Funded by State of Lower Saxony grant 14-76,103-184CORONA-11/20 and German Research Foundation, Excellence Strategy - EXC2155"RESIST"-Project ID39087428, and DFG-SFB900/3-Project ID158989968, grants SFB900-B3, SFB900-B8.
  • |Adult[MESH]
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |Betacoronavirus/*immunology[MESH]
  • |Biomarkers[MESH]
  • |CD4-Positive T-Lymphocytes/cytology/*immunology[MESH]
  • |CD8-Positive T-Lymphocytes/cytology/*immunology[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*immunology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunologic Memory/immunology[MESH]
  • |Lymphocyte Activation/*immunology[MESH]
  • |Lymphocyte Count[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*immunology[MESH]
  • |Prognosis[MESH]
  • |SARS-CoV-2[MESH]
  • |Severity of Illness Index[MESH]


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