In Vitro Antibody-Dependent Enhancement of SARS-CoV-2 Infection Could Be Abolished by Adding Human IgG

Author:

Wang Xun1,Li Minghui1,Lu Panpan2,Li Chen1,Zhao Chaoyue1,Zhao Xiaoyu1,Qiao Rui1,Cui Yuchen1,Chen Yanjia1,Li Jiayan1,Cai Guonan1,Wang Pengfei1ORCID

Affiliation:

1. Shanghai Pudong Hospital, Fudan University Pudong Medical Center, Shanghai Institute of Infectious Disease and Biosecurity, State Key Laboratory of Genetic Engineering, MOE Engineering Research Center of Gene Technology, School of Life Sciences, Fudan University, Shanghai 200438, China

2. Reproductive Center, Women and Children’s Hospital, Qingdao University, Qingdao 266001, China

Abstract

Evidence of antibody-dependent enhancement (ADE) of other viruses has raised concerns about the safety of SARS-CoV-2 vaccines and antibody therapeutics. In vitro studies have shown ADE of SARS-CoV-2 infection. In this study, we also found that vaccination/convalescent sera and some approved monoclonal antibodies can enhance SARS-CoV-2 infection of FcR-expressing B cells in vitro. However, the enhancement of SARS-CoV-2 infection can be prevented by blocking Fc–FcR interaction through the addition of human serum/IgG or the introduction of mutations in the Fc portion of the antibody. It should be noted that ADE activity observed on FcR-expressing cells in vitro may not necessarily reflect the situation in vivo; therefore, animal and clinical data should be included for ADE evaluation.

Funder

National Natural Science Foundation of China

Shanghai Rising-Star Program

Program of Science and Technology Cooperation with Hong Kong, Macao and Taiwan

Natural Science Foundation of Shandong Province

Open Research Fund of the State Key Laboratory of Genetic Engineering, Fudan University

Publisher

MDPI AG

Subject

Infectious Diseases,Microbiology (medical),General Immunology and Microbiology,Molecular Biology,Immunology and Allergy

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