COVID-19 Vaccine Reactogenicity and Immunogenicity
- Conditions
- COVID-19Vaccine Adverse ReactionVaccine Immune Response
- Registration Number
- NCT05258708
- Lead Sponsor
- Korea University Guro Hospital
- Brief Summary
Analysis of antibody kinetics after vaccination with mRNA-1273 and factors influencing the vaccine immunogenicity
- Detailed Description
We conducted a prospective study on healthy young adults who were to receive two doses of 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 addition, long-term anti-SARS-CoV-2 antibody kinetics will be assessed.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 179
- who were willing to receive the mRNA-1273 vaccine
- previously diagnosed with laboratory-confirmed COVID-19
- history of autoimmune disease
- immunocompromised, pregnant, or breastfeeding
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The correlation between humoral immune response and reactogenicity after vaccination The correlation between reactogenicity after dose 1 and immunogenicity at T1 (28 days after dose 1 prior to the 2nd dose) and T2 (28 days after dose 2); the correlation between reactogenicity after vaccine dose 2 and immunogenicity at T2 The correlation between humoral immune response and reactogenicity after vaccination
- Secondary Outcome Measures
Name Time Method neutralizing antibody titer before vaccination (T0), 28 days after the first dose prior to the second dose (T1), and 28 days after the second dose (T2) plaque reduction neutralization test was performed using wild-type SARS-CoV-2 virus (BetaCoV/Korea/KCDC03/2020)
Long-term persistence of anti-SARS-CoV-2 antibody and neutralizing antibody titer At 3 months and 6 months after dose 1 SARS-CoV-2 immunoglobulin G (IgG) assay (Abbott Laboratories, Chicago, IL, USA); plaque reduction neutralization test was performed using wild-type SARS-CoV-2 virus (BetaCoV/Korea/KCDC03/2020)
anti-SARS-CoV-2 antibody before vaccination (T0), 28 days after the first dose prior to the second dose (T1), and 28 days after the second dose (T2) SARS-CoV-2 immunoglobulin G (IgG) assay (Abbott Laboratories, Chicago, IL, USA)
reactogenicity after vaccination Seven days after each dose of vaccine record the occurrence, severity, and duration of solicited AEs using a standardized electronic questionnaire
Trial Locations
- Locations (5)
Korea University Anam Hospital
🇰🇷Seoul, Korea, Republic of
Catholic Kwandong University
🇰🇷Incheon, Korea, Republic of
Ajou University School of Medicine Hallym University
🇰🇷Suwon, Korea, Republic of
Kangnam Sacred Heart Hospital
🇰🇷Seoul, Korea, Republic of
Korea University Guro Hospital, International St. Mary's Hospital, Gangnam Sacred Heart Hospital, Ajou University School of Medicine, Korea University Anam Hospital
🇰🇷Seoul, Korea, Republic of