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

  • 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

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

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.

Original languageEnglish
Pages (from-to)73-80
Number of pages8
JournalInternational Journal of Infectious Diseases
Volume138
DOIs
StatePublished - Jan 2024

Bibliographical note

Publisher Copyright:
© 2023 The Author(s)

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • COVID-19
  • Durability
  • Humoral immunity
  • Liposome
  • RBD
  • SARS-CoV-2
  • Vaccine

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