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SARS‐CoV‐2 vaccination in solid‐organ transplant recipients: What the clinician needs to know
In response to the COVID‐19 pandemic, SARS‐CoV‐2 vaccines have been developed at an unparalleled speed, with 14 SARS‐CoV‐2 vaccines currently authorized. Solid‐organ transplant (SOT) recipients are at risk for developing a higher rate of COVID‐19‐related complications and therefore they are at prior...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8646251/ https://www.ncbi.nlm.nih.gov/pubmed/34450686 http://dx.doi.org/10.1111/tri.14029 |
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author | Giannella, Maddalena Pierrotti, Lígia C. Helanterä, Ilkka Manuel, Oriol |
author_facet | Giannella, Maddalena Pierrotti, Lígia C. Helanterä, Ilkka Manuel, Oriol |
author_sort | Giannella, Maddalena |
collection | PubMed |
description | In response to the COVID‐19 pandemic, SARS‐CoV‐2 vaccines have been developed at an unparalleled speed, with 14 SARS‐CoV‐2 vaccines currently authorized. Solid‐organ transplant (SOT) recipients are at risk for developing a higher rate of COVID‐19‐related complications and therefore they are at priority for immunization against SARS‐CoV‐2. Preliminary data suggest that although SARS‐CoV‐2 vaccines are safe in SOT recipients (with similar rate of adverse events than in the general population), the antibody responses are decreased in this population. Risk factors for poor vaccine immunogenicity include older age, shorter time from transplantation, use of mycophenolate and belatacept, and worse allograft function. SOT recipients should continue to be advised to maintain hand hygiene, use of facemasks, and social distancing after SARS‐CoV‐2 vaccine. Vaccination of household contacts should be also prioritized. Although highly encouraged for research purposes, systematic assessment in clinical practice of humoral and cellular immune responses after SARS‐CoV‐2 vaccination is controversial, since correlation between immunological findings and clinical protection from severe COVID‐19, and cutoffs for protection are currently unknown in SOT recipients. Alternative immunization schemes, including a booster dose, higher doses, and modulation of immunosuppression during vaccination, need to be assessed in the context of well‐designed clinical trials. |
format | Online Article Text |
id | pubmed-8646251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86462512021-12-06 SARS‐CoV‐2 vaccination in solid‐organ transplant recipients: What the clinician needs to know Giannella, Maddalena Pierrotti, Lígia C. Helanterä, Ilkka Manuel, Oriol Transpl Int Reviews in Clinical Transplantation In response to the COVID‐19 pandemic, SARS‐CoV‐2 vaccines have been developed at an unparalleled speed, with 14 SARS‐CoV‐2 vaccines currently authorized. Solid‐organ transplant (SOT) recipients are at risk for developing a higher rate of COVID‐19‐related complications and therefore they are at priority for immunization against SARS‐CoV‐2. Preliminary data suggest that although SARS‐CoV‐2 vaccines are safe in SOT recipients (with similar rate of adverse events than in the general population), the antibody responses are decreased in this population. Risk factors for poor vaccine immunogenicity include older age, shorter time from transplantation, use of mycophenolate and belatacept, and worse allograft function. SOT recipients should continue to be advised to maintain hand hygiene, use of facemasks, and social distancing after SARS‐CoV‐2 vaccine. Vaccination of household contacts should be also prioritized. Although highly encouraged for research purposes, systematic assessment in clinical practice of humoral and cellular immune responses after SARS‐CoV‐2 vaccination is controversial, since correlation between immunological findings and clinical protection from severe COVID‐19, and cutoffs for protection are currently unknown in SOT recipients. Alternative immunization schemes, including a booster dose, higher doses, and modulation of immunosuppression during vaccination, need to be assessed in the context of well‐designed clinical trials. John Wiley and Sons Inc. 2021-09-20 2021-10 /pmc/articles/PMC8646251/ /pubmed/34450686 http://dx.doi.org/10.1111/tri.14029 Text en © 2021 The Authors. Transplant International published by John Wiley & Sons Ltd on behalf of Steunstichting ESOT https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Reviews in Clinical Transplantation Giannella, Maddalena Pierrotti, Lígia C. Helanterä, Ilkka Manuel, Oriol SARS‐CoV‐2 vaccination in solid‐organ transplant recipients: What the clinician needs to know |
title | SARS‐CoV‐2 vaccination in solid‐organ transplant recipients: What the clinician needs to know |
title_full | SARS‐CoV‐2 vaccination in solid‐organ transplant recipients: What the clinician needs to know |
title_fullStr | SARS‐CoV‐2 vaccination in solid‐organ transplant recipients: What the clinician needs to know |
title_full_unstemmed | SARS‐CoV‐2 vaccination in solid‐organ transplant recipients: What the clinician needs to know |
title_short | SARS‐CoV‐2 vaccination in solid‐organ transplant recipients: What the clinician needs to know |
title_sort | sars‐cov‐2 vaccination in solid‐organ transplant recipients: what the clinician needs to know |
topic | Reviews in Clinical Transplantation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8646251/ https://www.ncbi.nlm.nih.gov/pubmed/34450686 http://dx.doi.org/10.1111/tri.14029 |
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