tetano
Editor, Senior Moderator
Front Immunol
. 2022 Jun 1;13:859019.
doi: 10.3389/fimmu.2022.859019. eCollection 2022.
Humoral and Cellular Responses to BNT162b2 as a Booster Following Two Doses of ChAdOx1 nCov-19 Determined Using Three SARS-CoV-2 Antibody Assays and an Interferon-Gamma Release Assay: A Prospective Longitudinal Study in Healthcare Workers
Seri Jeong[SUP] 1 [/SUP], Nuri Lee[SUP] 1 [/SUP], Su Kyung Lee[SUP] 2 [/SUP], Eun-Jung Cho[SUP] 2 [/SUP], Jungwon Hyun[SUP] 2 [/SUP], Min-Jeong Park[SUP] 1 [/SUP], Wonkeun Song[SUP] 1 [/SUP], Hyun Soo Kim[SUP] 2 [/SUP]
Affiliations
Abstract
Data on humoral and cellular responses to BNT162b2 as a booster dose, following two doses of ChAdOx1 nCov-19 vaccine, have seldom been reported. The aim of this study was to assess the positivity rates of three representative antibody assays targeting total, IgG, and neutralizing antibodies, and an interferon-γ release assay (IGRA), and to determine the longitudinal changes in quantitative antibody titers after each vaccination. A total of 1027 samples were collected from healthcare workers. The number of participants after the booster dose was 153, and they all completed a questionnaire on adverse reactions. All antibody assays showed 100.0% positivity at 1 month after booster vaccination. The median antibody titers of the assays were significantly increased compared with those after the second dose (22.1-fold increase for Roche total antibody, 14.0-fold increase for Abbott IgG, and 1.1-fold increase (97.5% inhibition) for GenScript neutralizing antibody). Cellular responses determined using the IGRA were positive in 92.8% of the participants. Most participants (72.5%) reported mild adverse reactions. Correlations between the three antibody assays and IGRA were weak or negligible, indicating a difference between humoral and cellular responses. Overall, our study provides information about booster vaccine strategies and laboratory settings, which could subsequently contribute to the control of the spread of coronavirus disease 2019.
Keywords: BNT162b2; ChAdOx1 nCov-19; INF-γ; SARS-CoV-2; antibody; assay; booster; vaccine.
. 2022 Jun 1;13:859019.
doi: 10.3389/fimmu.2022.859019. eCollection 2022.
Humoral and Cellular Responses to BNT162b2 as a Booster Following Two Doses of ChAdOx1 nCov-19 Determined Using Three SARS-CoV-2 Antibody Assays and an Interferon-Gamma Release Assay: A Prospective Longitudinal Study in Healthcare Workers
Seri Jeong[SUP] 1 [/SUP], Nuri Lee[SUP] 1 [/SUP], Su Kyung Lee[SUP] 2 [/SUP], Eun-Jung Cho[SUP] 2 [/SUP], Jungwon Hyun[SUP] 2 [/SUP], Min-Jeong Park[SUP] 1 [/SUP], Wonkeun Song[SUP] 1 [/SUP], Hyun Soo Kim[SUP] 2 [/SUP]
Affiliations
- PMID: 35720318
- PMCID: PMC9198331
- DOI: 10.3389/fimmu.2022.859019
Abstract
Data on humoral and cellular responses to BNT162b2 as a booster dose, following two doses of ChAdOx1 nCov-19 vaccine, have seldom been reported. The aim of this study was to assess the positivity rates of three representative antibody assays targeting total, IgG, and neutralizing antibodies, and an interferon-γ release assay (IGRA), and to determine the longitudinal changes in quantitative antibody titers after each vaccination. A total of 1027 samples were collected from healthcare workers. The number of participants after the booster dose was 153, and they all completed a questionnaire on adverse reactions. All antibody assays showed 100.0% positivity at 1 month after booster vaccination. The median antibody titers of the assays were significantly increased compared with those after the second dose (22.1-fold increase for Roche total antibody, 14.0-fold increase for Abbott IgG, and 1.1-fold increase (97.5% inhibition) for GenScript neutralizing antibody). Cellular responses determined using the IGRA were positive in 92.8% of the participants. Most participants (72.5%) reported mild adverse reactions. Correlations between the three antibody assays and IGRA were weak or negligible, indicating a difference between humoral and cellular responses. Overall, our study provides information about booster vaccine strategies and laboratory settings, which could subsequently contribute to the control of the spread of coronavirus disease 2019.
Keywords: BNT162b2; ChAdOx1 nCov-19; INF-γ; SARS-CoV-2; antibody; assay; booster; vaccine.