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      Predictive Value of Reactogenicity for Anti-SARS-CoV-2 Antibody Response in mRNA-1273 Recipients: A Multicenter Prospective Cohort Study.

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          Abstract

          Messenger RNA (mRNA) vaccination was developed to mitigate the coronavirus disease 2019 pandemic. However, data on antibody kinetics and factors influencing these vaccines' immunogenicity are limited. We conducted a prospective study on healthy young adults who received two doses of the mRNA-1273 vaccine at 28-day intervals. After each dose, adverse events were prospectively evaluated, and blood samples were collected. The correlation between humoral immune response and reactogenicity after vaccination was determined. In 177 participants (19-55 years), the geometric mean titers of anti-S IgG antibody were 178.07 and 4409.61 U/mL, while those of 50% neutralizing titers were 479.95 and 2851.67 U/mL four weeks after the first and second vaccine doses, respectively. Anti-S IgG antibody titers were not associated with local reactogenicity but were higher in participants who experienced systemic adverse events (headache and muscle pain). Antipyretic use was an independent predictive factor of a robust anti-SARS-CoV-2 antibody response after receiving both vaccine doses. Systemic reactogenicity after the first dose influenced antibody response after the second dose. In conclusion, mRNA-1273 induced a robust antibody response in healthy young adults. Antipyretic use did not decrease the anti-SARS-CoV-2 antibody response after mRNA-1273 vaccination.

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          Author and article information

          Journal
          Vaccines (Basel)
          Vaccines
          MDPI AG
          2076-393X
          2076-393X
          Jan 03 2023
          : 11
          : 1
          Affiliations
          [1 ] Department of Internal Medicine, International St. Mary's Hospital, Catholic Kwandong University College of Medicine, Incheon 22711, Republic of Korea.
          [2 ] Department of Infectious Diseases, Ajou University School of Medicine, Suwon 16499, Republic of Korea.
          [3 ] Division of Infectious Diseases, Department of Internal Medicine, Kangnam Sacred Heart Hospital, Hallym University College of Medicine, Seoul 07441, Republic of Korea.
          [4 ] Department of Internal Medicine, Korea University Anam Hospital, Korea University College of Medicine, Seoul 02841, Republic of Korea.
          [5 ] Department of Internal Medicine, Korea University Guro Hospital, Korea University College of Medicine, Seoul 08308, Republic of Korea.
          [6 ] Vaccine Innovation Center-KU Medicine (VIC-K), Seoul 08308, Republic of Korea.
          [7 ] Division of Vaccine Clinical Research Center for Vaccine Research, National Institute of Infectious Diseases, Cheongju 28159, Republic of Korea.
          Article
          vaccines11010120
          10.3390/vaccines11010120
          9862064
          36679965
          5a1ec641-efae-4cdb-b862-ec0f2e730f53
          History

          COVID-19,vaccine,reactogenicity,immunogenicity,SARS-CoV-2
          COVID-19, vaccine, reactogenicity, immunogenicity, SARS-CoV-2

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