Kinetics of adaptive immune responses after administering mRNA-Based COVID-19 vaccination in individuals with and without prior SARS-CoV-2 infections

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dc.contributor.authorS W Yoon-
dc.contributor.authorK Widyasari-
dc.contributor.authorJ Jang-
dc.contributor.authorS Lee-
dc.contributor.authorTaejoon Kang-
dc.contributor.authorS Kim-
dc.date.accessioned2023-10-30T16:33:04Z-
dc.date.available2023-10-30T16:33:04Z-
dc.date.issued2023-
dc.identifier.issn1471-2334-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/32914-
dc.description.abstractObjective: We aimed to compare the adaptive immune response in individuals with or without prior SARS-CoV-2 infections following the administration of mRNA-based COVID-19 vaccines. Methods: A total of 54 participants with ages ranging from 37 to 56 years old, consisting of 23 individuals without a history of SARS-CoV-2 infection (uninfected group) and 31 individuals with prior infection of SARS-CoV-2 (infected group) who have received two doses of mRNA SARS-CoV-2 vaccines were enrolled in this study. We measured the IFN-γ level upon administration of BNT162b2 (PF) or mRNA-1273 (MO) by QuantiFERON SARS-CoV-2. The production of neutralizing antibodies was evaluated by a surrogate virus neutralization assay, and the neutralizing capacity was assessed by a plaque reduction neutralization test (PRNT50). The immune response was compared between the two groups. Results: A significantly higher level of IFN-γ (p < 0.001) and neutralization antibodies (p < 0.001) were observed in the infected group than those in the uninfected group following the first administration of vaccines. The infected group demonstrated a significantly higher PRNT50 titer than the uninfected group against the Wuhan strain (p < 0.0001). Still, the two groups were not significantly different against Delta (p = 0.07) and Omicron (p = 0.14) variants. Following the second vaccine dose, T- and B-cell levels were not significantly increased in the infected group. Conclusion: A single dose of mRNA-based COVID-19 vaccines would boost immune responses in individuals who had previously contracted SARS-CoV-2.-
dc.publisherSpringer-BMC-
dc.titleKinetics of adaptive immune responses after administering mRNA-Based COVID-19 vaccination in individuals with and without prior SARS-CoV-2 infections-
dc.title.alternativeKinetics of adaptive immune responses after administering mRNA-Based COVID-19 vaccination in individuals with and without prior SARS-CoV-2 infections-
dc.typeArticle-
dc.citation.titleBMC Infectious Diseases-
dc.citation.number0-
dc.citation.endPage732-
dc.citation.startPage732-
dc.citation.volume23-
dc.contributor.affiliatedAuthorTaejoon Kang-
dc.contributor.alternativeName윤선우-
dc.contributor.alternativeNameWidyasari-
dc.contributor.alternativeName장지은-
dc.contributor.alternativeName이승준-
dc.contributor.alternativeName강태준-
dc.contributor.alternativeName김선주-
dc.identifier.bibliographicCitationBMC Infectious Diseases, vol. 23, pp. 732-732-
dc.identifier.doi10.1186/s12879-023-08728-5-
dc.subject.keywordCOVID-19-
dc.subject.keywordmRNA vaccine-
dc.subject.keywordImmune response-
dc.subject.keywordIFN-γ-
dc.subject.keywordNeutralizing antibody-
dc.subject.localCOVID-19-
dc.subject.localCovid19-
dc.subject.localCOVID19-
dc.subject.localCCOVID 19-
dc.subject.localCOVID?19-
dc.subject.localmRNA vaccine-
dc.subject.localImmune response-
dc.subject.localimmune response-
dc.subject.localImmune responses-
dc.subject.localIFN-gamma-
dc.subject.localIFN-γ-
dc.subject.localIfn-γ-
dc.subject.localNeutralizing antibody-
dc.subject.localneutralizing antibody-
dc.subject.localNeutrallizing antibody-
dc.subject.localNeutralizing antibofdy-
dc.subject.localneutrallizing antibody-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
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