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

被引:359
作者
Arvin, Ann M. [1 ,2 ]
Fink, Katja [1 ,3 ]
Schmid, Michael A. [1 ,3 ]
Cathcart, Andrea [1 ]
Spreafico, Roberto [1 ]
Havenar-Daughton, Colin [1 ]
Lanzavecchia, Antonio [1 ,3 ]
Corti, Davide [1 ,3 ]
Virgin, Herbert W. [1 ,4 ]
机构
[1] Vir Biotechnol, San Francisco, CA 94158 USA
[2] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[3] Humabs Biomed SA, Bellinzona, Switzerland
[4] Washington Univ, Sch Med, St Louis, MO 63110 USA
关键词
RESPIRATORY SYNDROME CORONAVIRUS; HUMAN MONOCLONAL-ANTIBODY; PARAINFLUENZA VIRUS-VACCINE; SARS-CORONAVIRUS; CONVALESCENT PLASMA; EFFECTOR FUNCTIONS; PROTECTIVE EFFICACY; SPIKE GLYCOPROTEIN; IMMUNE-RESPONSE; INFECTION;
D O I
10.1038/s41586-020-2538-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The antibody-dependent enhancement of disease is reviewed, with an emphasis on implications for the prevention and treatment of SARS-CoV-2 infection. 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.
引用
收藏
页码:353 / 363
页数:11
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