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Comparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study

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dc.contributor.authorKang , Ji man-
dc.contributor.authorLee, Ju Han-
dc.contributor.authorHuh, Kyu Ha-
dc.contributor.authorJoo, Dong Jin-
dc.contributor.authorLEE, JAE GEUN-
dc.contributor.authorKim, Ha Yan-
dc.contributor.authorLee, Myeongjee-
dc.contributor.authorJung, In Kyung-
dc.contributor.authorKim, Min Young-
dc.contributor.authorKim, Sin Young-
dc.contributor.authorPark, Youn Hee-
dc.contributor.authorKim, Myoung Soo-
dc.date.accessioned2023-03-22T02:05:26Z-
dc.date.available2023-03-22T02:05:26Z-
dc.date.created2023-04-14-
dc.date.issued2023-02-
dc.identifier.issn1386-6532-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/193521-
dc.description.abstractBackground: : Solid organ transplant recipients (SOTRs) are susceptible to severe coronavirus disease 2019 (COVID-19); however, immunogenicity studies of the Omicron variants per vaccination schedules are still lacking. We examined humoral immunogenicity following third-dose mRNA vaccine administration in Korean SOTRs who received primary COVID-19 vaccine series on homologous or heterologous schedules.Methods: : We recruited SOTRs at Severance Hospital from October 27, 2021, to March 31, 2022. Blood samples were collected between 14 days and 5 months after the second and third mRNA vaccine (BNT162b2 or mRNA-1273) doses. SARS-CoV-2 anti-spike IgG titer was analyzed. The neutralization inhibition rate was analyzed using the surrogate neutralization assay for the wild-type, Delta, and Omicron variants.Results: : No significant differences existed in the SARS-CoV-2 anti-spike IgG positivity rate between the ho-mologous BNT162b2/BNT162b2/BNT162b2 (85%) and other heterologous groups (83% of ChAdOx1/ChA-dOx1/BNT162b2, 90% of ChAdOx1/ChAdOx1/mRNA-1273, and 78% of ChAdOx1/BNT162b2/BNT162b2). No significant difference existed in the neutralization inhibition rates between the four groups for wild-type, Delta, and Omicron variants. Median neutralization inhibition rates against the Omicron variant (2-5%) were signif-icantly lower than those against the wild-type (87-97%) and Delta (55-89%) variants (P < 0.001).Conclusions: : Regardless of the schedule, the neutralization inhibition rate against the Omicron variant was poor; therefore, additional preventive measures are required in such high-risk populations.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherElsevier Science-
dc.relation.isPartOfJournal of Clinical Virology-
dc.relation.isPartOfJOURNAL OF CLINICAL VIROLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleComparison of humoral immunogenicity in solid organ transplant recipients after third-dose mRNA vaccine with homologous or heterologous schedules: An observational study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Pediatrics (소아과학교실)-
dc.contributor.googleauthorKang , Ji man-
dc.contributor.googleauthorLee, Ju Han-
dc.contributor.googleauthorHuh, Kyu Ha-
dc.contributor.googleauthorJoo, Dong Jin-
dc.contributor.googleauthorLEE, JAE GEUN-
dc.contributor.googleauthorKim, Ha Yan-
dc.contributor.googleauthorLee, Myeongjee-
dc.contributor.googleauthorJung, In Kyung-
dc.contributor.googleauthorKim, Min Young-
dc.contributor.googleauthorKim, Sin Young-
dc.contributor.googleauthorPark, Youn Hee-
dc.contributor.googleauthorKim, Myoung Soo-
dc.identifier.doi10.1016/j.jcv.2022.105374-
dc.relation.journalcodeJ01343-
dc.identifier.eissn1873-5967-
dc.identifier.pmid36592547-
dc.subject.keywordCOVID-19 vaccine-
dc.subject.keywordSARS-CoV-2 variants-
dc.subject.keywordOrgan transplantation-
dc.subject.keywordHeterologous-
dc.subject.keywordKorea-
dc.subject.keywordOmicron-
dc.contributor.alternativeNameKang, Ji-Man-
dc.contributor.affiliatedAuthorKang , Ji man-
dc.contributor.affiliatedAuthorLee, Ju Han-
dc.contributor.affiliatedAuthorHuh, Kyu Ha-
dc.contributor.affiliatedAuthorJoo, Dong Jin-
dc.contributor.affiliatedAuthorLEE, JAE GEUN-
dc.contributor.affiliatedAuthorKim, Ha Yan-
dc.contributor.affiliatedAuthorLee, Myeongjee-
dc.contributor.affiliatedAuthorJung, In Kyung-
dc.contributor.affiliatedAuthorKim, Min Young-
dc.contributor.affiliatedAuthorKim, Sin Young-
dc.contributor.affiliatedAuthorPark, Youn Hee-
dc.contributor.affiliatedAuthorKim, Myoung Soo-
dc.identifier.scopusid2-s2.0-85145329350-
dc.identifier.wosid000918593900001-
dc.citation.volume159-
dc.identifier.bibliographicCitationJournal of Clinical Virology, Vol.159, 2023-02-
dc.identifier.rimsid78409-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorCOVID-19 vaccine-
dc.subject.keywordAuthorSARS-CoV-2 variants-
dc.subject.keywordAuthorOrgan transplantation-
dc.subject.keywordAuthorHeterologous-
dc.subject.keywordAuthorKorea-
dc.subject.keywordAuthorOmicron-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryVirology-
dc.relation.journalResearchAreaVirology-
dc.identifier.articleno105374-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Biomedical Systems Informatics (의생명시스템정보학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers

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