Reduced neutralization and Fc effector function to Omicron subvariants in sera from SARS‐CoV‐1 survivors after two doses of CoronaVac plus one dose subunit vaccine

Author:

Chen Danying1234,Li Xinglin1234,Hao Xiaohua13,Qiu Yaruo125,Song Yanjun1234,Sun Hui1234,Liu Yongmei1234,Du Juan1234,Zhang Yuanyuan1234,Xiao Fan1234,Song Chuan1234,Yan Yonghong1234,Song Rui13,Wang Xi1234,Zhao Xuesen1234ORCID,Jin Ronghua1234

Affiliation:

1. Beijing Key Laboratory of Emerging Infectious Diseases, Institute of Infectious Diseases, Beijing Ditan Hospital Capital Medical University Beijing China

2. Beijing Institute of Infectious Diseases Beijing China

3. National Center for Infectious Diseases, Beijing Ditan Hospital Capital Medical University Beijing China

4. National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases Beijing China

5. Peking University Ditan Teaching Hospital Beijing China

Abstract

AbstractSevere acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) Omicron harbors more than 30 mutations of the spike protein and exhibits substantial immune evasion. Although previous study indicated that BNT162b2 messenger RNA vaccine induces potent cross‐clade pan‐sarbecovirus neutralizing antibodies in survivors of the infection by SARS‐CoV‐1, the neutralization activity and Fc‐mediated effector functions of these cross‐reactive antibodies elicited in SARS‐CoV‐1 survivors to Omicron subvariants still remain largely unknown. In this study, the neutralization activity and Fc‐mediated effector functions of antibodies boosted by a third dose vaccination were characterized in SARS‐CoV‐1 convalescents and healthy individuals. Potent cross‐clade broadly neutralizing antibodies were observed in SARS‐CoV‐1 survivors who received a three‐dose vaccination regimen consisting of two priming doses of CoronaVac followed by one booster dose of the protein subunit vaccine ZF2001. However, the induced antibodies exhibited both reduced neutralization and impaired Fc effector functions targeting multiple Omicron subvariants. Importantly, the data also support the notion that immune imprints resulted from SARS‐CoV‐1 infection may exacerbate the impairment of neutralization activity and Fc‐mediated effector functions to Omicron subvariants and provided invaluable information to vaccination strategy in future.

Publisher

Wiley

Subject

Infectious Diseases,Virology

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