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Fourth BNT162b2 vaccination neutralization of omicron infection after heart transplantation
We investigated changes in receptor-binding domain IgG and neutralizing antibodies against the omicron and delta variants, vs the wild-type virus, in response to a fourth BNT162b2 dose in 90 heart transplant (HT) recipients. The fourth dose induced anti-RBD IgG antibodies and a higher neutralization...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Society for Heart and Lung Transplantation.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068265/ https://www.ncbi.nlm.nih.gov/pubmed/35794051 http://dx.doi.org/10.1016/j.healun.2022.04.014 |
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author | Peled, Yael Afek, Arnon Nemet, Ital Rahav, Galia Raanani, Ehud Patel, Jignesh K. Mandelboim, Michal |
author_facet | Peled, Yael Afek, Arnon Nemet, Ital Rahav, Galia Raanani, Ehud Patel, Jignesh K. Mandelboim, Michal |
author_sort | Peled, Yael |
collection | PubMed |
description | We investigated changes in receptor-binding domain IgG and neutralizing antibodies against the omicron and delta variants, vs the wild-type virus, in response to a fourth BNT162b2 dose in 90 heart transplant (HT) recipients. The fourth dose induced anti-RBD IgG antibodies and a higher neutralization efficiency against the wild-type virus and the variants; however, neutralization efficiency against the omicron variant was lower than that against the delta variant (the latter demonstrating efficacy similar to that against the wild-type virus). Notably, while IgG anti-RBD antibodies were detectable in >80% of the HT recipients, only about half demonstrated neutralization efficiency against the omicron variant. A SARS-CoV-2-specific-T-cell response following the fourth dose was evident in the majority of transplant recipients. Boosting vulnerable groups improves antibody responses (including neutralizing responses) and cellular immunity, but the incomplete immunological response, particularly for omicron, suggests continued preventive measures and optimization of vaccination strategies that elicit strong, and long-lasting immune responses, in this high-risk population, should remain a priority. |
format | Online Article Text |
id | pubmed-9068265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | International Society for Heart and Lung Transplantation. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90682652022-05-05 Fourth BNT162b2 vaccination neutralization of omicron infection after heart transplantation Peled, Yael Afek, Arnon Nemet, Ital Rahav, Galia Raanani, Ehud Patel, Jignesh K. Mandelboim, Michal J Heart Lung Transplant Article We investigated changes in receptor-binding domain IgG and neutralizing antibodies against the omicron and delta variants, vs the wild-type virus, in response to a fourth BNT162b2 dose in 90 heart transplant (HT) recipients. The fourth dose induced anti-RBD IgG antibodies and a higher neutralization efficiency against the wild-type virus and the variants; however, neutralization efficiency against the omicron variant was lower than that against the delta variant (the latter demonstrating efficacy similar to that against the wild-type virus). Notably, while IgG anti-RBD antibodies were detectable in >80% of the HT recipients, only about half demonstrated neutralization efficiency against the omicron variant. A SARS-CoV-2-specific-T-cell response following the fourth dose was evident in the majority of transplant recipients. Boosting vulnerable groups improves antibody responses (including neutralizing responses) and cellular immunity, but the incomplete immunological response, particularly for omicron, suggests continued preventive measures and optimization of vaccination strategies that elicit strong, and long-lasting immune responses, in this high-risk population, should remain a priority. International Society for Heart and Lung Transplantation. 2022-09 2022-05-05 /pmc/articles/PMC9068265/ /pubmed/35794051 http://dx.doi.org/10.1016/j.healun.2022.04.014 Text en © 2022 International Society for Heart and Lung Transplantation. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Peled, Yael Afek, Arnon Nemet, Ital Rahav, Galia Raanani, Ehud Patel, Jignesh K. Mandelboim, Michal Fourth BNT162b2 vaccination neutralization of omicron infection after heart transplantation |
title | Fourth BNT162b2 vaccination neutralization of omicron infection after heart transplantation |
title_full | Fourth BNT162b2 vaccination neutralization of omicron infection after heart transplantation |
title_fullStr | Fourth BNT162b2 vaccination neutralization of omicron infection after heart transplantation |
title_full_unstemmed | Fourth BNT162b2 vaccination neutralization of omicron infection after heart transplantation |
title_short | Fourth BNT162b2 vaccination neutralization of omicron infection after heart transplantation |
title_sort | fourth bnt162b2 vaccination neutralization of omicron infection after heart transplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9068265/ https://www.ncbi.nlm.nih.gov/pubmed/35794051 http://dx.doi.org/10.1016/j.healun.2022.04.014 |
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