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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...

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Autores principales: Giannella, Maddalena, Pierrotti, Lígia C., Helanterä, Ilkka, Manuel, Oriol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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