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Immune Response Kinetics Following a Third Heterologous BNT162b2 Booster Dose After Primary 2-Dose ChAdOx1 Vaccination in Relation to Omicron Breakthrough Infection: A Prospective Nationwide Cohort Study in South Korea

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dc.contributor.author김용찬-
dc.contributor.author박윤수-
dc.contributor.author송영구-
dc.contributor.author안진영-
dc.contributor.author이경화-
dc.contributor.author최준용-
dc.date.accessioned2024-01-03T01:30:16Z-
dc.date.available2024-01-03T01:30:16Z-
dc.date.issued2023-07-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/197571-
dc.description.abstractBackground: Immune responses to each vaccine must be investigated to establish effective vaccination strategies for the ongoing coronavirus disease (COVID-19) pandemic. We investigated the long-term kinetics of immune responses after heterologous booster vaccination in relation to Omicron breakthrough infection (BI). Methods: Our study included 373 healthcare workers who received primary ChAdOx1 vaccine doses and a third BNT162b2 vaccine dose. BIs that occurred after the third vaccine were investigated. Blood specimens were collected before and 3 months after the booster dose from participants without BI and 1, 4, and 6 months after BI from participants who experienced BI. Spike-specific binding and neutralizing antibody levels against the wild-type virus, Omicron BA.1, and Omicron BA.5, as well as cellular responses, were analyzed. Results: A total of 346 participants (82 in the no BI group; 192 in the BI group during the BA.1/BA.2 period; 72 in the BI group during the BA.5 period) were included in the analysis. Participants without BI exhibited the highest binding and neutralizing antibody concentrations and greatest cellular response 1 month after the third vaccination, which reached a nadir by the ninth month. Antibody and cellular responses in participants who experienced BI substantially increased postinfection. Neutralizing antibody titers in individuals who experienced BI during the BA.1/BA.2 period showed more robust increase against wild-type virus than against BA.1 and BA.5. Conclusions: Our findings provide evidence of antigenic imprinting in participants who received a heterologous booster vaccination, thereby serving as a foundation for further studies on the impact of BIs on immune responses.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherOxford University Press on behalf of the Infectious Diseases Society of America-
dc.relation.isPartOfOPEN FORUM INFECTIOUS DISEASES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleImmune Response Kinetics Following a Third Heterologous BNT162b2 Booster Dose After Primary 2-Dose ChAdOx1 Vaccination in Relation to Omicron Breakthrough Infection: A Prospective Nationwide Cohort Study in South Korea-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorJin Young Ahn-
dc.contributor.googleauthorJae-Hoon Ko-
dc.contributor.googleauthorKyong Ran Peck-
dc.contributor.googleauthorSeongman Bae-
dc.contributor.googleauthorSung-Han Kim-
dc.contributor.googleauthorKyoung Hwa Lee-
dc.contributor.googleauthorYoung Goo Song-
dc.contributor.googleauthorYong Chan Kim-
dc.contributor.googleauthorYoon Soo Park-
dc.contributor.googleauthorKyoung-Ho Song-
dc.contributor.googleauthorEu Suk Kim-
dc.contributor.googleauthorHye Won Jeong-
dc.contributor.googleauthorShin-Woo Kim-
dc.contributor.googleauthorKi Tae Kwon-
dc.contributor.googleauthorWon Suk Choi-
dc.contributor.googleauthorJun Yong Choi-
dc.identifier.doi10.1093/ofid/ofad363-
dc.contributor.localIdA00752-
dc.contributor.localIdA01598-
dc.contributor.localIdA02037-
dc.contributor.localIdA02267-
dc.contributor.localIdA04620-
dc.contributor.localIdA04191-
dc.relation.journalcodeJ03621-
dc.identifier.eissn2328-8957-
dc.identifier.pmid37520424-
dc.subject.keywordCOVID-19-
dc.subject.keywordOmicron breakthrough infection-
dc.subject.keywordantigen imprinting-
dc.subject.keywordcoronavirus disease-
dc.subject.keywordheterologous booster vaccination-
dc.contributor.alternativeNameKim, Yong Chan-
dc.contributor.affiliatedAuthor김용찬-
dc.contributor.affiliatedAuthor박윤수-
dc.contributor.affiliatedAuthor송영구-
dc.contributor.affiliatedAuthor안진영-
dc.contributor.affiliatedAuthor이경화-
dc.contributor.affiliatedAuthor최준용-
dc.citation.volume10-
dc.citation.number7-
dc.citation.startPageofad363-
dc.identifier.bibliographicCitationOPEN FORUM INFECTIOUS DISEASES, Vol.10(7) : ofad363, 2023-07-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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