Antibody Responses to the SARS-CoV-2 Ancestral Strain and Omicron Variants in Moderna mRNA-1273 Vaccinated Active-Duty US Navy Sailors and Marines

Author:

Sun Peifang1,Balinsky Corey A12,Jiang Le12,Jani Vihasi12,Long Tran Khanh3,Cheng Ying14,Serote Mary Ann3,Smith Andrew B5,Fears Burnetta F5,Gatrell Stephanie K14,Sugiharto Victor A12,Chen Huawei12,Zhang Zhiwen12,Belinskaya Tatyana12,Qiu Qi12,Graham William D1,Schilling Megan A1,Jones Anthony R6,Corson Karen S7,Martin Nicholas J7,Letizia Andrew G7,Hontz Robert D7

Affiliation:

1. Naval Medical Research Center , Silver Spring, Maryland , USA

2. Henry Jackson Foundation for the Advancement of Military Medicine , Bethesda, Maryland , USA

3. Vysnova Partners, Inc , Landover, Maryland , USA

4. Leidos , Reston, Virginia , USA

5. Third Marine Logistics Group , Okinawa , Japan

6. Armed Forces Research Institute of Medical Sciences , Bangkok , Thailand

7. US Naval Medical Research Unit TWO , Singapore , Singapore

Abstract

Abstract Omicron and its subvariants have steadily gained greater capability of immune escape compared to other variants of concern, resulting in an increased incidence of reinfections even among vaccinated individuals. We evaluated the antibody response to Omicron BA.1, BA.2, and BA.4/5 in US military members vaccinated with the primary 2-dose series of Moderna mRNA-1273 in a cross-sectional study. While nearly all vaccinated participants had sustained spike (S) IgG and neutralizing antibodies (ND50) to the ancestral strain, only 7.7% participants had detectable ND50 to Omicron BA.1 at 8 months postvaccination. The neutralizing antibody response to BA.2 and BA.5 was similarly reduced. The reduced antibody neutralization of Omicron correlated with the decreased antibody binding to the receptor-binding domain. The participants’ seropositivity to the nuclear protein positively correlated with ND50. Our data emphasizes the need for continuous vigilance in monitoring for emerging variants and the need to identify potential alternative targets for vaccine design.

Funder

Joint Program Executive Office

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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