DC Field | Value | Language |
---|---|---|
dc.contributor.author | S W Yoon | - |
dc.contributor.author | K Widyasari | - |
dc.contributor.author | J Jang | - |
dc.contributor.author | S Lee | - |
dc.contributor.author | Taejoon Kang | - |
dc.contributor.author | S Kim | - |
dc.date.accessioned | 2023-10-30T16:33:04Z | - |
dc.date.available | 2023-10-30T16:33:04Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 1471-2334 | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/32914 | - |
dc.description.abstract | Objective: 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.publisher | Springer-BMC | - |
dc.title | Kinetics of adaptive immune responses after administering mRNA-Based COVID-19 vaccination in individuals with and without prior SARS-CoV-2 infections | - |
dc.title.alternative | Kinetics of adaptive immune responses after administering mRNA-Based COVID-19 vaccination in individuals with and without prior SARS-CoV-2 infections | - |
dc.type | Article | - |
dc.citation.title | BMC Infectious Diseases | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 732 | - |
dc.citation.startPage | 732 | - |
dc.citation.volume | 23 | - |
dc.contributor.affiliatedAuthor | Taejoon Kang | - |
dc.contributor.alternativeName | 윤선우 | - |
dc.contributor.alternativeName | Widyasari | - |
dc.contributor.alternativeName | 장지은 | - |
dc.contributor.alternativeName | 이승준 | - |
dc.contributor.alternativeName | 강태준 | - |
dc.contributor.alternativeName | 김선주 | - |
dc.identifier.bibliographicCitation | BMC Infectious Diseases, vol. 23, pp. 732-732 | - |
dc.identifier.doi | 10.1186/s12879-023-08728-5 | - |
dc.subject.keyword | COVID-19 | - |
dc.subject.keyword | mRNA vaccine | - |
dc.subject.keyword | Immune response | - |
dc.subject.keyword | IFN-γ | - |
dc.subject.keyword | Neutralizing antibody | - |
dc.subject.local | COVID-19 | - |
dc.subject.local | Covid19 | - |
dc.subject.local | COVID19 | - |
dc.subject.local | CCOVID 19 | - |
dc.subject.local | COVID?19 | - |
dc.subject.local | mRNA vaccine | - |
dc.subject.local | Immune response | - |
dc.subject.local | immune response | - |
dc.subject.local | Immune responses | - |
dc.subject.local | IFN-gamma | - |
dc.subject.local | IFN-γ | - |
dc.subject.local | Ifn-γ | - |
dc.subject.local | Neutralizing antibody | - |
dc.subject.local | neutralizing antibody | - |
dc.subject.local | Neutrallizing antibody | - |
dc.subject.local | Neutralizing antibofdy | - |
dc.subject.local | neutrallizing antibody | - |
dc.description.journalClass | Y | - |
There are no files associated with this item.
Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.