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One-year antibody durability induced by EuCorVac-19, a liposome-displayed COVID-19 receptor binding domain subunit vaccine, in healthy Korean subjects

Authors :
Jonathan F. Lovell
Kazutoyo Miura
Yeong Ok Baik
Chankyu Lee
Jeong-Yoon Lee
Young-Shin Park
Ingi Hong
Jung Hyuk Lee
Taewoo Kim
Sang Hwan Seo
Jae-Ouk Kim
Manki Song
Chung-Jong Kim
Jae-Ki Choi
Jieun Kim
Eun Ju Choo
Jung-Hyun Choi
Source :
International Journal of Infectious Diseases, Vol 138, Iss , Pp 73-80 (2024)
Publication Year :
2024
Publisher :
Elsevier, 2024.

Abstract

Objective: EuCorVac-19 (ECV-19), an adjuvanted liposome-displayed receptor binding domain (RBD) COVID-19 vaccine, previously reported interim Phase 2 trial results showing induction of neutralizing antibodies 3 weeks after prime-boost immunization. The objective of this study was to determine the longer-term antibody response of the vaccine. Methods: To assess immunogenicity 6 and 12 months after vaccination, participants in the Phase 2 trial (NCT04783311) were excluded if they: 1) withdrew, 2) reported COVID-19 infection or additional vaccination, or 3) exhibited increasing Spike (S) antibodies (representing possible non-reported infection). Following exclusions, of the 197 initial subjects, anti-S IgG antibodies and neutralizing antibodies were further assessed in 124 subjects at the 6-month timepoint, and 36 subjects at the 12-month timepoint. Results: Median anti-S antibody half-life was 52 days (interquartile range [IQR]:42-70), in the “early” period from 3 weeks to 6 months, and 130 days (IQR:97-169) in the “late” period from 6 to 12 months. There was a negative correlation between initial antibody titer and half-life. Anti-S and neutralizing antibody responses were correlated. Neutralizing antibody responses showed longer half-lives; the early period had a median half-life of 120 days (IQR:81-207), and the late period had a median half-life of 214 days (IQR:140-550). Conclusion: These data establish antibody durability of ECV-19, using a framework to analyze COVID-19 vaccine-induced antibodies during periods of high infection.

Details

Language :
English
ISSN :
12019712
Volume :
138
Issue :
73-80
Database :
Directory of Open Access Journals
Journal :
International Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.92e258add5c642e19060a10330ea19f8
Document Type :
article
Full Text :
https://doi.org/10.1016/j.ijid.2023.11.004