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Immune Assessment of BNT162b2 m-RNA-Spike Based Vaccine Response in Adults
Vaccine efficacy is based on clinical data. Currently, the assessment of immune response after SARS-CoV-2 vaccination is scarce. A total of 52 healthcare workers were immunized with the same lot of BNT162b2 vaccine. The immunological response against the vaccine was tested using a T-specific assay b...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389701/ https://www.ncbi.nlm.nih.gov/pubmed/34440072 http://dx.doi.org/10.3390/biomedicines9080868 |
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author | San Segundo, David Comins-Boo, Alejandra Irure-Ventura, Juan Renuncio-García, Mónica Roa-Bautista, Adriel González-López, Elena Merino-Fernández, David Lamadrid-Perojo, Patricia Alonso-Peña, Marta Ocejo-Vinyals, Javier Gonzalo Gutiérrez-Larrañaga, Maria Guiral-Foz, Sandra López-Hoyos, Marcos |
author_facet | San Segundo, David Comins-Boo, Alejandra Irure-Ventura, Juan Renuncio-García, Mónica Roa-Bautista, Adriel González-López, Elena Merino-Fernández, David Lamadrid-Perojo, Patricia Alonso-Peña, Marta Ocejo-Vinyals, Javier Gonzalo Gutiérrez-Larrañaga, Maria Guiral-Foz, Sandra López-Hoyos, Marcos |
author_sort | San Segundo, David |
collection | PubMed |
description | Vaccine efficacy is based on clinical data. Currently, the assessment of immune response after SARS-CoV-2 vaccination is scarce. A total of 52 healthcare workers were immunized with the same lot of BNT162b2 vaccine. The immunological response against the vaccine was tested using a T-specific assay based on the expression of CD25 and CD134 after stimulation with anti-N, -S, and -M specific peptides of SARS-CoV-2. Moreover, IgG anti-S2 and -RBD antibodies were detected using ELISA. Furthermore, the cell subsets involved in the response to the vaccine were measured in peripheral blood by flow cytometry. Humoral-specific responses against the vaccine were detected in 94% and 100% after the first and second doses, respectively. Therefore, anti-S T-specific responses were observed in 57% and 90% of the subjects after the first and second doses of the vaccine, respectively. Thirty days after the second dose, significant increases in T helper 1 memory cells (p < 0.001), peripheral memory T follicular helper (pT(FH)) cells (p < 0.032), and switched memory (p = 0.005) were observed. This study describes the specific humoral and cellular immune responses after vaccination with the new mRNA-based BNT162b2 vaccine. A mobilization of T(FH) into the circulation occurs, reflecting a specific activation of the immune system. |
format | Online Article Text |
id | pubmed-8389701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83897012021-08-27 Immune Assessment of BNT162b2 m-RNA-Spike Based Vaccine Response in Adults San Segundo, David Comins-Boo, Alejandra Irure-Ventura, Juan Renuncio-García, Mónica Roa-Bautista, Adriel González-López, Elena Merino-Fernández, David Lamadrid-Perojo, Patricia Alonso-Peña, Marta Ocejo-Vinyals, Javier Gonzalo Gutiérrez-Larrañaga, Maria Guiral-Foz, Sandra López-Hoyos, Marcos Biomedicines Article Vaccine efficacy is based on clinical data. Currently, the assessment of immune response after SARS-CoV-2 vaccination is scarce. A total of 52 healthcare workers were immunized with the same lot of BNT162b2 vaccine. The immunological response against the vaccine was tested using a T-specific assay based on the expression of CD25 and CD134 after stimulation with anti-N, -S, and -M specific peptides of SARS-CoV-2. Moreover, IgG anti-S2 and -RBD antibodies were detected using ELISA. Furthermore, the cell subsets involved in the response to the vaccine were measured in peripheral blood by flow cytometry. Humoral-specific responses against the vaccine were detected in 94% and 100% after the first and second doses, respectively. Therefore, anti-S T-specific responses were observed in 57% and 90% of the subjects after the first and second doses of the vaccine, respectively. Thirty days after the second dose, significant increases in T helper 1 memory cells (p < 0.001), peripheral memory T follicular helper (pT(FH)) cells (p < 0.032), and switched memory (p = 0.005) were observed. This study describes the specific humoral and cellular immune responses after vaccination with the new mRNA-based BNT162b2 vaccine. A mobilization of T(FH) into the circulation occurs, reflecting a specific activation of the immune system. MDPI 2021-07-22 /pmc/articles/PMC8389701/ /pubmed/34440072 http://dx.doi.org/10.3390/biomedicines9080868 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article San Segundo, David Comins-Boo, Alejandra Irure-Ventura, Juan Renuncio-García, Mónica Roa-Bautista, Adriel González-López, Elena Merino-Fernández, David Lamadrid-Perojo, Patricia Alonso-Peña, Marta Ocejo-Vinyals, Javier Gonzalo Gutiérrez-Larrañaga, Maria Guiral-Foz, Sandra López-Hoyos, Marcos Immune Assessment of BNT162b2 m-RNA-Spike Based Vaccine Response in Adults |
title | Immune Assessment of BNT162b2 m-RNA-Spike Based Vaccine Response in Adults |
title_full | Immune Assessment of BNT162b2 m-RNA-Spike Based Vaccine Response in Adults |
title_fullStr | Immune Assessment of BNT162b2 m-RNA-Spike Based Vaccine Response in Adults |
title_full_unstemmed | Immune Assessment of BNT162b2 m-RNA-Spike Based Vaccine Response in Adults |
title_short | Immune Assessment of BNT162b2 m-RNA-Spike Based Vaccine Response in Adults |
title_sort | immune assessment of bnt162b2 m-rna-spike based vaccine response in adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8389701/ https://www.ncbi.nlm.nih.gov/pubmed/34440072 http://dx.doi.org/10.3390/biomedicines9080868 |
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