Correlates of Nucleocapsid Antibodies and a Combination of Spike and Nucleocapsid Antibodies Against Protection of SARS-CoV-2 Infection During the Omicron XBB.1.16/EG.5–Predominant Wave

Author:

Yamamoto Shohei1ORCID,Oshiro Yusuke2,Inamura Natsumi2,Nemoto Takashi2,Tan Tomofumi2,Horii Kumi3,Okudera Kaori4,Konishi Maki1,Mizoue Tetsuya1ORCID,Sugiyama Haruhito5,Aoyanagi Nobuyoshi6,Sugiura Wataru7,Ohmagari Norio8ORCID

Affiliation:

1. Department of Epidemiology and Prevention, Center for Clinical Sciences, National Center for Global Health and Medicine , Tokyo , Japan

2. Department of Laboratory Testing, Center Hospital of the National Center for the Global Health and Medicine , Tokyo , Japan

3. Infection Control Office, Center Hospital of the National Center for the Global Health and Medicine , Tokyo , Japan

4. Infection Control Office, Kohnodai Hospital of the National Center for the Global Health and Medicine , Chiba , Japan

5. Center Hospital of the National Center for the Global Health and Medicine , Tokyo , Japan

6. Kohnodai Hospital of the National Center for the Global Health and Medicine , Chiba , Japan

7. Center for Clinical Sciences, National Center for Global Health and Medicine , Tokyo , Japan

8. Disease Control and Prevention Center, National Center for Global Health and Medicine , Tokyo , Japan

Abstract

Abstract Background We aimed to examine the association among nucleocapsid (N) antibodies, a combination of N and spike (S) antibodies, and protection against SARS-CoV-2 reinfection. Methods We conducted a prospective cohort study among staff at a national medical research center in Tokyo and followed them for the incidence of SARS-CoV-2 infection between June and September 2023 (Omicron XBB.1.16/EG.5 wave). At baseline, participants donated blood samples to measure N- and S-specific antibodies. Cox regression was used to estimate the hazard ratio and protection ([1 – hazard ratio] × 100) against subsequent SARS-CoV-2 infection across these antibody levels. Results Among participants with previous infection, higher pre-reinfection N antibodies were associated with a lower risk of reinfection, even after adjusting S antibody levels (P < .01 for trend). Estimation of the protection matrix for N and S antibodies revealed that high levels in N and S antibodies conferred robust protection (>90%) against subsequent infection. In addition, a pattern of low pre-reinfection N antibodies but high vaccine-enhanced S antibodies showed high protection (>80%). Conclusions Pre-reinfection N antibody levels correlated with protection against reinfection, independent of S antibodies. If the N antibodies were low, vaccine-boosted S antibodies might enhance the reinfection protection.

Funder

NCGM COVID-19 Gift Fund

Japan Health Research Promotion Bureau Research Fund

National Center for Global Health and Medicine

Abbott Japan and Roche Diagnostics

, which

Publisher

Oxford University Press (OUP)

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