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Cross-neutralizing antibody responses among individuals with or without bivalent vaccine: a six-month prospective cohort studyopen access:Cross-neutralizing antibody responses among individuals with or without bivalent vaccine : a six-month prospective cohort study

Other Titles
:Cross-neutralizing antibody responses among individuals with or without bivalent vaccine : a six-month prospective cohort study
Authors
Cha, Hye HeeKim, Ji YeunKim, Seung BeomCha, JunhoKwon, Ji-SooKim, WooriSon, Ju YeonJang, Choi YoungKim, Min-ChulLim, So YunKim, Sung-Han
Issue Date
May-2026
Publisher
대한내과학회
Keywords
Antibodies, Neutralizing; Bivalent vaccine; COVID-19; Neutralization tests; SARS-CoV-2
Citation
Korean Journal of Internal Medicine, v.41, no.3, pp 516 - 523
Pages
8
Indexed
SCIE
SCOPUS
KCI
Journal Title
Korean Journal of Internal Medicine
Volume
41
Number
3
Start Page
516
End Page
523
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/212766
DOI
10.3904/kjim.2025.246
ISSN
1226-3303
2005-6648
Abstract
Background/Aims: Although the COVID-19 pandemic has officially ended, SARS-CoV-2 continues to circulate with periodic surges and may exhibit seasonal patterns. Understanding the importance of prompt immunization, particularly in individuals with prior infection, is crucial for developing future vaccination protocols. This study aimed to assess the durability and breadth of neutralizing antibody (nAb) responses against Omicron subvariants based on infection and bivalent vaccination status. Methods: In this six-month prospective cohort study, we evaluated nAb responses to the original SARS-CoV-2 strain (D614G), as well as Omicron subvariants BA.4/5 and XBB.1.5 variants, in 79 healthcare workers stratified by prior Omicron infection and bivalent vaccination status. Blood samples were collected at baseline, 3 months, and 6 months, and nAb titers were measured using an optimized pseudovirus neutralization assay. Results: At 3 months, individuals with prior Omicron infection followed by bivalent vaccination showed significantly higher nAb titers against BA.4/5 and XBB.1.5 compared to those with infection alone or vaccination alone. At 6 months, the highest titers persisted in the group with both prior infection and bivalent vaccination, while titers declined in previously infected but unvaccinated individuals. Notably, individuals with prior infection alone exhibited comparable nAb titers to infection-naïve vaccinated individuals, suggesting limited durability of infection-induced immunity without vaccine-induced boosting. Conclusions: These findings underscore the importance of timely vaccination, even among previously infected individuals, to ensure sustained humoral immunity and broader cross-nAb responses against emerging SARS-CoV-2 variants.
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서울 의과대학 (DEPARTMENT OF MEDICAL MICROBIOLOGY)
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