Neutralizing Antibodies Against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants Induced by Natural Infection or Vaccination: A Systematic Review and Pooled Analysis

Author:

Chen Xinhua1,Chen Zhiyuan1,Azman Andrew S23,Sun Ruijia1,Lu Wanying1,Zheng Nan1,Zhou Jiaxin1,Wu Qianhui1,Deng Xiaowei1,Zhao Zeyao1,Chen Xinghui1,Ge Shijia4,Yang Juan1,Leung Daniel T56,Yu Hongjie147ORCID

Affiliation:

1. School of Public Health, Fudan University, Key Laboratory of Public Health Safety, Ministry of Education, Shanghai, China

2. Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA

3. Institute of Global Health, Faculty of Medicine, University of Geneva, Geneva, Switzerland

4. Department of Infectious Diseases, Huashan Hospital, Fudan University, Shanghai, China

5. Division of Infectious Diseases, University of Utah School of Medicine, Salt Lake City, Utah, USA

6. Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, Utah, USA

7. Shanghai Institute of Infectious Disease and Biosecurity, Fudan University, Shanghai, China

Abstract

Abstract Recently emerged severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants may pose a threat to immunity. A systematic landscape of neutralizing antibodies against emerging variants is needed. We systematically searched for studies that evaluated neutralizing antibody titers induced by previous infection or vaccination against SARS-CoV-2 variants and collected individual data. We identified 106 studies meeting the eligibility criteria. Lineage B.1.351 (beta), P.1 (gamma) and B.1.617.2 (delta) significantly escaped natural infection–mediated neutralization, with an average of 4.1-fold (95% confidence interval [CI]: 3.6–4.7-fold), 1.8-fold (1.4–2.4-fold), and 3.2-fold (2.4–4.1-fold) reduction in live virus neutralization assay, while neutralizing titers against B.1.1.7 (alpha) decreased slightly (1.4-fold [95% CI: 1.2–1.6-fold]). Serum from vaccinees also led to significant reductions in neutralization of B.1.351 across different platforms, with an average of 7.1-fold (95% CI: 5.5–9.0-fold) for nonreplicating vector platform, 4.1-fold (3.7–4.4-fold) for messenger RNA platform, and 2.5-fold (1.7–2.9-fold) for protein subunit platform. Neutralizing antibody levels induced by messenger RNA vaccines against SARS-CoV-2 variants were similar to, or higher, than that derived from naturally infected individuals.

Funder

National Science Fund for Distinguished Young Scholars

Program of Shanghai Academic/Technology Research Leader

National Science and Technology Major project of China

US National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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