tetano
Editor, Senior Moderator
Front Immunol
. 2022 Mar 24;13:856657.
doi: 10.3389/fimmu.2022.856657. eCollection 2022.
Specific Anti-SARS-CoV-2 Humoral and Cellular Immune Responses After Booster Dose of BNT162b2 Pfizer-BioNTech mRNA-Based Vaccine: Integrated Study of Adaptive Immune System Components
Rosalia Busà[SUP] 1 [/SUP], Maria Concetta Sorrentino[SUP] 2 [/SUP], Giovanna Russelli[SUP] 1 [/SUP], Giandomenico Amico[SUP] 1 3 [/SUP], Vitale Miceli[SUP] 1 [/SUP], Monica Miele[SUP] 1 3 [/SUP], Mariangela Di Bella[SUP] 1 3 [/SUP], Francesca Timoneri[SUP] 1 3 [/SUP], Alessia Gallo[SUP] 1 [/SUP], Giovanni Zito[SUP] 1 [/SUP], Daniele Di Carlo[SUP] 2 [/SUP], Pier Giulio Conaldi[SUP] 1 [/SUP], Matteo Bulati[SUP] 1 [/SUP]
Affiliations
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes coronavirus disease 2019 (COVID-19), is modifying human activity all over the world with significant health and economic burden. The advent of the SARS-CoV-2 pandemic prompted the scientific community to learn the virus dynamics concerning transmissibility, epidemiology, and usefulness of vaccines in fighting emerging health hazards. Pieces of evidence suggest that the first and second doses of mRNA vaccines induce a significant antibody response in vaccinated subjects or patients who recovered from SARS-CoV-2 infection, demonstrating the importance of the previously formed memory. The aim of this work has been to investigate the effects of BNT162b2 Pfizer-BioNTech mRNA-based vaccine booster dose in a cohort of 11 uninfected immunocompetent (ICs), evaluating the humoral and cellular responses, with more carefulness on memory B and T cells. Our findings underscore the potential benefit of the third dose of mRNA vaccine on the lifespan of memory B and T cells, suggesting that booster doses could increase protection against SARS-CoV-2 infection.
Keywords: B cells; BNT162b2; SARS-CoV-2; T cells; booster dose; mRNA vaccine.
. 2022 Mar 24;13:856657.
doi: 10.3389/fimmu.2022.856657. eCollection 2022.
Specific Anti-SARS-CoV-2 Humoral and Cellular Immune Responses After Booster Dose of BNT162b2 Pfizer-BioNTech mRNA-Based Vaccine: Integrated Study of Adaptive Immune System Components
Rosalia Busà[SUP] 1 [/SUP], Maria Concetta Sorrentino[SUP] 2 [/SUP], Giovanna Russelli[SUP] 1 [/SUP], Giandomenico Amico[SUP] 1 3 [/SUP], Vitale Miceli[SUP] 1 [/SUP], Monica Miele[SUP] 1 3 [/SUP], Mariangela Di Bella[SUP] 1 3 [/SUP], Francesca Timoneri[SUP] 1 3 [/SUP], Alessia Gallo[SUP] 1 [/SUP], Giovanni Zito[SUP] 1 [/SUP], Daniele Di Carlo[SUP] 2 [/SUP], Pier Giulio Conaldi[SUP] 1 [/SUP], Matteo Bulati[SUP] 1 [/SUP]
Affiliations
- PMID: 35401503
- PMCID: PMC8987231
- DOI: 10.3389/fimmu.2022.856657
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which causes coronavirus disease 2019 (COVID-19), is modifying human activity all over the world with significant health and economic burden. The advent of the SARS-CoV-2 pandemic prompted the scientific community to learn the virus dynamics concerning transmissibility, epidemiology, and usefulness of vaccines in fighting emerging health hazards. Pieces of evidence suggest that the first and second doses of mRNA vaccines induce a significant antibody response in vaccinated subjects or patients who recovered from SARS-CoV-2 infection, demonstrating the importance of the previously formed memory. The aim of this work has been to investigate the effects of BNT162b2 Pfizer-BioNTech mRNA-based vaccine booster dose in a cohort of 11 uninfected immunocompetent (ICs), evaluating the humoral and cellular responses, with more carefulness on memory B and T cells. Our findings underscore the potential benefit of the third dose of mRNA vaccine on the lifespan of memory B and T cells, suggesting that booster doses could increase protection against SARS-CoV-2 infection.
Keywords: B cells; BNT162b2; SARS-CoV-2; T cells; booster dose; mRNA vaccine.