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10.3389/fimmu.2020.567710

http://scihub22266oqcxt.onion/10.3389/fimmu.2020.567710
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33178193!7594548!33178193
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suck abstract from ncbi


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pmid33178193      Front+Immunol 2020 ; 11 (ä): 567710
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  • Is Cross-Reactive Immunity Triggering COVID-19 Immunopathogenesis? #MMPMID33178193
  • Beretta A; Cranage M; Zipeto D
  • Front Immunol 2020[]; 11 (ä): 567710 PMID33178193show ga
  • The serological responses to both SARS-CoV-1 and SARS-CoV-2 virus have some unique characteristics that suggest cross-reactive priming by other human coronaviruses (hCoVs). The early kinetics and magnitude of these responses are, in some cases, associated with worse clinical outcomes in SARS and COVID-19. Cross-reactive hCoV antibody responses have been detected in both SARS and COVID-19 patients. There is also evidence that pre-existing T cell immunity to common cold coronaviruses can prime the response to SARS-CoV-2. Studies in non-human primates show that SARS-CoV-1 S-protein vaccine-induced antibodies are associated with acute lung injury in macaques challenged with SARS-CoV-1. Here we discuss the potential of cross-reactive immunity to drive the immunopathogenesis of COVID-19 and its implications for current efforts to develop immune-based therapies and vaccines.
  • |Animals[MESH]
  • |Antibodies, Viral/*immunology[MESH]
  • |Antibody-Dependent Enhancement[MESH]
  • |CD4-Positive T-Lymphocytes/immunology[MESH]
  • |COVID-19/*immunology/prevention & control/therapy/virology[MESH]
  • |Cross Reactions[MESH]
  • |Humans[MESH]
  • |Immunologic Memory[MESH]
  • |SARS-CoV-2/*immunology[MESH]
  • |Severe Acute Respiratory Syndrome/*immunology/prevention & control/therapy/virology[MESH]
  • |Severe acute respiratory syndrome-related coronavirus/*immunology[MESH]


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