Neutralizing Antibody Activity to Severe Acute Respiratory Syndrome Coronavirus 2 Delta (B.1.617.2) and Omicron (B.1.1.529) After 1 or 2 Doses of BNT162b2 Vaccine in Infection-Naive and Previously Infected Individuals

Author:

Moy James N1,Anderson Mark2,Shen Xiaoying3,Fu Jia1,Stec Michael2,Gosha Amy1,Naquiallah Dina1,Kinslow Jennifer1,Montefiori David C3,Cloherty Gavin2,Landay Alan1

Affiliation:

1. Division of Allergy and Immunology and Division of Gerontology, Department of Internal Medicine, Rush University Medical Center, Rush University , Chicago, Illinois , USA

2. Abbott Laboratories, Abbott Diagnostics Division , Abbott Park, Illinois , USA

3. Department of Surgery and Duke Human Vaccine Institute, Duke University Medical Center , Durham, North Carolina , USA

Abstract

Abstract Previous reports demonstrated that severe acute respiratory syndrome coronavirus (SARS-CoV-2) binding immunoglobulin G levels did not increase significantly between the first and second doses of the BNT162b2 vaccine in previously infected individuals. We tested neutralizing antibodies (nAbs) against SARS-CoV-2 Delta and Omicron variants after the first and second doses of this vaccine in infection-naive and previously infected individuals. Delta, but not Omicron, nAb titers significantly increased from the first to the second dose in both groups of individuals. Importantly, we found that Omicron nAb titers were much lower than Delta nAb titers and that even after 2 doses of vaccine, 17 of 29 individuals in the infection-naive group and 2 of 27 in the previously infected group did not have detectable Omicron nAb titers. Infection history alone did not adequately predict whether a second dose resulted in adequate nAb. For future variants of concern, the discussion on the optimal number of vaccine doses should be based on studies testing for nAb against the specific variant.

Funder

Abbott Diagnostics Division Research and Development

Department of Health and Human Services

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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