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A perspective on potential antibody-dependent enhancement of SARS-CoV-2

Author

Listed:
  • Ann M. Arvin

    (Vir Biotechnology
    Stanford University School of Medicine)

  • Katja Fink

    (Vir Biotechnology
    a subsidiary of Vir Biotechnology)

  • Michael A. Schmid

    (Vir Biotechnology
    a subsidiary of Vir Biotechnology)

  • Andrea Cathcart

    (Vir Biotechnology)

  • Roberto Spreafico

    (Vir Biotechnology)

  • Colin Havenar-Daughton

    (Vir Biotechnology)

  • Antonio Lanzavecchia

    (Vir Biotechnology
    a subsidiary of Vir Biotechnology)

  • Davide Corti

    (Vir Biotechnology
    a subsidiary of Vir Biotechnology)

  • Herbert W. Virgin

    (Vir Biotechnology
    Washington University School of Medicine)

Abstract

Antibody-dependent enhancement (ADE) of disease is a general concern for the development of vaccines and antibody therapies because the mechanisms that underlie antibody protection against any virus have a theoretical potential to amplify the infection or trigger harmful immunopathology. This possibility requires careful consideration at this critical point in the pandemic of coronavirus disease 2019 (COVID-19), which is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Here we review observations relevant to the risks of ADE of disease, and their potential implications for SARS-CoV-2 infection. At present, there are no known clinical findings, immunological assays or biomarkers that can differentiate any severe viral infection from immune-enhanced disease, whether by measuring antibodies, T cells or intrinsic host responses. In vitro systems and animal models do not predict the risk of ADE of disease, in part because protective and potentially detrimental antibody-mediated mechanisms are the same and designing animal models depends on understanding how antiviral host responses may become harmful in humans. The implications of our lack of knowledge are twofold. First, comprehensive studies are urgently needed to define clinical correlates of protective immunity against SARS-CoV-2. Second, because ADE of disease cannot be reliably predicted after either vaccination or treatment with antibodies—regardless of what virus is the causative agent—it will be essential to depend on careful analysis of safety in humans as immune interventions for COVID-19 move forward.

Suggested Citation

  • Ann M. Arvin & Katja Fink & Michael A. Schmid & Andrea Cathcart & Roberto Spreafico & Colin Havenar-Daughton & Antonio Lanzavecchia & Davide Corti & Herbert W. Virgin, 2020. "A perspective on potential antibody-dependent enhancement of SARS-CoV-2," Nature, Nature, vol. 584(7821), pages 353-363, August.
  • Handle: RePEc:nat:nature:v:584:y:2020:i:7821:d:10.1038_s41586-020-2538-8
    DOI: 10.1038/s41586-020-2538-8
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    Cited by:

    1. Dapeng Li & David R. Martinez & Alexandra Schäfer & Haiyan Chen & Maggie Barr & Laura L. Sutherland & Esther Lee & Robert Parks & Dieter Mielke & Whitney Edwards & Amanda Newman & Kevin W. Bock & Mahn, 2022. "Breadth of SARS-CoV-2 neutralization and protection induced by a nanoparticle vaccine," Nature Communications, Nature, vol. 13(1), pages 1-15, December.

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