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10.1038/s41564-020-00789-5

http://scihub22266oqcxt.onion/10.1038/s41564-020-00789-5
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32908214!ä!32908214

suck abstract from ncbi


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pmid32908214      Nat+Microbiol 2020 ; 5 (10): 1185-1191
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  • Antibody-dependent enhancement and SARS-CoV-2 vaccines and therapies #MMPMID32908214
  • Lee WS; Wheatley AK; Kent SJ; DeKosky BJ
  • Nat Microbiol 2020[Oct]; 5 (10): 1185-1191 PMID32908214show ga
  • Antibody-based drugs and vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are being expedited through preclinical and clinical development. Data from the study of SARS-CoV and other respiratory viruses suggest that anti-SARS-CoV-2 antibodies could exacerbate COVID-19 through antibody-dependent enhancement (ADE). Previous respiratory syncytial virus and dengue virus vaccine studies revealed human clinical safety risks related to ADE, resulting in failed vaccine trials. Here, we describe key ADE mechanisms and discuss mitigation strategies for SARS-CoV-2 vaccines and therapies in development. We also outline recently published data to evaluate the risks and opportunities for antibody-based protection against SARS-CoV-2.
  • |*Antibody-Dependent Enhancement/immunology[MESH]
  • |*Betacoronavirus/immunology[MESH]
  • |Animals[MESH]
  • |Antibodies, Monoclonal/administration & dosage[MESH]
  • |Antibodies, Neutralizing/administration & dosage[MESH]
  • |Antibodies, Viral/administration & dosage/immunology[MESH]
  • |COVID-19[MESH]
  • |COVID-19 Drug Treatment[MESH]
  • |COVID-19 Serotherapy[MESH]
  • |COVID-19 Vaccines[MESH]
  • |Coronavirus Infections/drug therapy/*immunology/prevention & control/*therapy[MESH]
  • |Humans[MESH]
  • |Immunization, Passive/adverse effects[MESH]
  • |In Vitro Techniques[MESH]
  • |Models, Immunological[MESH]
  • |Pandemics/prevention & control[MESH]
  • |Pneumonia, Viral/*immunology/prevention & control/*therapy[MESH]
  • |Respiratory Tract Diseases/etiology/immunology[MESH]
  • |Risk Factors[MESH]
  • |SARS-CoV-2[MESH]
  • |Safety[MESH]


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