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10.1002/eji.202048908

http://scihub22266oqcxt.onion/10.1002/eji.202048908
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33073359!ä!33073359

suck abstract from ncbi


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pmid33073359      Eur+J+Immunol 2020 ; 50 (12): 1998-2012
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  • Divergent SARS-CoV-2-specific T- and B-cell responses in severe but not mild COVID-19 patients #MMPMID33073359
  • Oja AE; Saris A; Ghandour CA; Kragten NAM; Hogema BM; Nossent EJ; Heunks LMA; Cuvalay S; Slot E; Linty F; Swaneveld FH; Vrielink H; Vidarsson G; Rispens T; van der Schoot E; van Lier RAW; Ten Brinke A; Hombrink P
  • Eur J Immunol 2020[Dec]; 50 (12): 1998-2012 PMID33073359show ga
  • Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the current coronavirus disease 2019 (COVID-19) pandemic. Understanding the immune response that provides specific immunity but may also lead to immunopathology is crucial for the design of potential preventive and therapeutic strategies. Here, we characterized and quantified SARS-CoV-2-specific immune responses in patients with different clinical courses. Compared to individuals with a mild clinical presentation, CD4(+) T-cell responses were qualitatively impaired in critically ill patients. Strikingly, however, in these patients the specific IgG antibody response was remarkably strong. Furthermore, in these critically ill patients, a massive influx of circulating T cells into the lungs was observed, overwhelming the local T-cell compartment, and indicative of vascular leakage. The observed disparate T- and B-cell responses could be indicative of a deregulated immune response in critically ill COVID-19 patients.
  • |Adult[MESH]
  • |Aged[MESH]
  • |Antibodies, Viral/*immunology[MESH]
  • |B-Lymphocytes/*immunology/pathology[MESH]
  • |CD4-Positive T-Lymphocytes/*immunology/pathology[MESH]
  • |COVID-19/*immunology/pathology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Immunoglobulin G/*immunology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |SARS-CoV-2/*immunology[MESH]


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