Antibody-dependent enhancement and SARS-CoV-2 vaccines and therapies

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 thr...

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Published inNature microbiology Vol. 5; no. 10; pp. 1185 - 1191
Main Authors Lee, Wen Shi, Wheatley, Adam K., Kent, Stephen J., DeKosky, Brandon J.
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.10.2020
Nature Publishing Group
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Abstract 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. Mechanisms of antibody-dependent enhancement of disease and mitigation strategies for SARS-CoV-2 vaccines and therapies are discussed.
AbstractList 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-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-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-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.Mechanisms of antibody-dependent enhancement of disease and mitigation strategies for SARS-CoV-2 vaccines and therapies are discussed.
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. Mechanisms of antibody-dependent enhancement of disease and mitigation strategies for SARS-CoV-2 vaccines and therapies are discussed.
Author Kent, Stephen J.
DeKosky, Brandon J.
Lee, Wen Shi
Wheatley, Adam K.
Author_xml – sequence: 1
  givenname: Wen Shi
  orcidid: 0000-0001-7285-4054
  surname: Lee
  fullname: Lee, Wen Shi
  organization: Department of Microbiology and Immunology, University of Melbourne at the Peter Doherty Institute for Infection and Immunity
– sequence: 2
  givenname: Adam K.
  orcidid: 0000-0002-5593-9387
  surname: Wheatley
  fullname: Wheatley, Adam K.
  organization: Department of Microbiology and Immunology, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, ARC Centre for Excellence in Convergent Bio-Nano Science and Technology, University of Melbourne
– sequence: 3
  givenname: Stephen J.
  orcidid: 0000-0002-8539-4891
  surname: Kent
  fullname: Kent, Stephen J.
  email: skent@unimelb.edu.au
  organization: Department of Microbiology and Immunology, University of Melbourne at the Peter Doherty Institute for Infection and Immunity, ARC Centre for Excellence in Convergent Bio-Nano Science and Technology, University of Melbourne, Melbourne Sexual Health Centre and Department of Infectious Diseases, Alfred Hospital and Central Clinical School, Monash University
– sequence: 4
  givenname: Brandon J.
  orcidid: 0000-0001-6406-0836
  surname: DeKosky
  fullname: DeKosky, Brandon J.
  email: dekosky@ku.edu
  organization: Department of Pharmaceutical Chemistry, The University of Kansas, Department of Chemical Engineering, The University of Kansas, Bioengineering Graduate Program, The University of Kansas
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32908214$$D View this record in MEDLINE/PubMed
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Snippet Antibody-based drugs and vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are being expedited through preclinical and clinical...
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pubmed
crossref
springer
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StartPage 1185
SubjectTerms 13/1
631/250/255
631/61/24
Animals
Antibodies
Antibodies, Monoclonal - administration & dosage
Antibodies, Neutralizing - administration & dosage
Antibodies, Viral - administration & dosage
Antibodies, Viral - immunology
Antibody-Dependent Enhancement - immunology
Betacoronavirus - immunology
Biomedical and Life Sciences
Clinical trials
Coronavirus Infections - drug therapy
Coronavirus Infections - immunology
Coronavirus Infections - prevention & control
Coronavirus Infections - therapy
Coronaviruses
COVID-19
COVID-19 Drug Treatment
COVID-19 Serotherapy
COVID-19 Vaccines
Dengue fever
Humans
Immunization, Passive - adverse effects
In Vitro Techniques
Infectious Diseases
Life Sciences
Medical Microbiology
Microbiology
Models, Immunological
Pandemics - prevention & control
Parasitology
Perspective
Pneumonia, Viral - immunology
Pneumonia, Viral - prevention & control
Pneumonia, Viral - therapy
Respiratory syncytial virus
Respiratory Tract Diseases - etiology
Respiratory Tract Diseases - immunology
Risk Factors
Safety
SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2
Vaccines
Viral Vaccines - adverse effects
Viral Vaccines - immunology
Virology
Title Antibody-dependent enhancement and SARS-CoV-2 vaccines and therapies
URI https://link.springer.com/article/10.1038/s41564-020-00789-5
https://www.ncbi.nlm.nih.gov/pubmed/32908214
https://www.proquest.com/docview/2474988359
https://www.proquest.com/docview/2441607890
Volume 5
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