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Effectiveness, Immunogenicity and Harms of Additional SARS-CoV-2 Vaccine Doses in Kidney Transplant Recipients: A Systematic Review

Background: Kidney transplant recipients (KTRs) who have a highly impaired immune response are in need of intensified and safe vaccination strategies to achieve seroconversion and prevent severe disease. Methods: We searched the Web of Science Core Collection, the Cochrane COVID-19 Study Register an...

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Autores principales: Hausinger, Renate Ilona, Bachmann, Quirin, Crone-Rawe, Timotius, Hannane, Nora, Monsef, Ina, Haller, Bernhard, Heemann, Uwe, Skoetz, Nicole, Kreuzberger, Nina, Schmaderer, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141039/
https://www.ncbi.nlm.nih.gov/pubmed/37112775
http://dx.doi.org/10.3390/vaccines11040863
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author Hausinger, Renate Ilona
Bachmann, Quirin
Crone-Rawe, Timotius
Hannane, Nora
Monsef, Ina
Haller, Bernhard
Heemann, Uwe
Skoetz, Nicole
Kreuzberger, Nina
Schmaderer, Christoph
author_facet Hausinger, Renate Ilona
Bachmann, Quirin
Crone-Rawe, Timotius
Hannane, Nora
Monsef, Ina
Haller, Bernhard
Heemann, Uwe
Skoetz, Nicole
Kreuzberger, Nina
Schmaderer, Christoph
author_sort Hausinger, Renate Ilona
collection PubMed
description Background: Kidney transplant recipients (KTRs) who have a highly impaired immune response are in need of intensified and safe vaccination strategies to achieve seroconversion and prevent severe disease. Methods: We searched the Web of Science Core Collection, the Cochrane COVID-19 Study Register and the WHO COVID-19 global literature on coronavirus disease from January 2020 to 22 July 2022 for prospective studies that assessed immunogenicity and efficacy after three or more SARS-CoV-2 vaccine doses. Results: In 37 studies on 3429 patients, de novo seroconversion after three and four vaccine doses ranged from 32 to 60% and 25 to 37%. Variant-specific neutralization was 59 to 70% for Delta and 12 to 52% for Omicron. Severe disease after infection was rarely reported but all concerned KTRs lacked immune responses after vaccination. Studies investigating the clinical course of COVID-19 found remarkably higher rates of severe disease than in the general population. Serious adverse events and acute graft rejections were very rare. Substantial heterogeneity between the studies limited their comparability and summary. Conclusion: Additional SARS-CoV-2 vaccine doses are potent and safe in general terms as well as regarding transplant-specific outcomes whilst the Omicron wave remains a significant threat to KTRs without adequate immune responses.
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spelling pubmed-101410392023-04-29 Effectiveness, Immunogenicity and Harms of Additional SARS-CoV-2 Vaccine Doses in Kidney Transplant Recipients: A Systematic Review Hausinger, Renate Ilona Bachmann, Quirin Crone-Rawe, Timotius Hannane, Nora Monsef, Ina Haller, Bernhard Heemann, Uwe Skoetz, Nicole Kreuzberger, Nina Schmaderer, Christoph Vaccines (Basel) Systematic Review Background: Kidney transplant recipients (KTRs) who have a highly impaired immune response are in need of intensified and safe vaccination strategies to achieve seroconversion and prevent severe disease. Methods: We searched the Web of Science Core Collection, the Cochrane COVID-19 Study Register and the WHO COVID-19 global literature on coronavirus disease from January 2020 to 22 July 2022 for prospective studies that assessed immunogenicity and efficacy after three or more SARS-CoV-2 vaccine doses. Results: In 37 studies on 3429 patients, de novo seroconversion after three and four vaccine doses ranged from 32 to 60% and 25 to 37%. Variant-specific neutralization was 59 to 70% for Delta and 12 to 52% for Omicron. Severe disease after infection was rarely reported but all concerned KTRs lacked immune responses after vaccination. Studies investigating the clinical course of COVID-19 found remarkably higher rates of severe disease than in the general population. Serious adverse events and acute graft rejections were very rare. Substantial heterogeneity between the studies limited their comparability and summary. Conclusion: Additional SARS-CoV-2 vaccine doses are potent and safe in general terms as well as regarding transplant-specific outcomes whilst the Omicron wave remains a significant threat to KTRs without adequate immune responses. MDPI 2023-04-18 /pmc/articles/PMC10141039/ /pubmed/37112775 http://dx.doi.org/10.3390/vaccines11040863 Text en © 2023 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 Systematic Review
Hausinger, Renate Ilona
Bachmann, Quirin
Crone-Rawe, Timotius
Hannane, Nora
Monsef, Ina
Haller, Bernhard
Heemann, Uwe
Skoetz, Nicole
Kreuzberger, Nina
Schmaderer, Christoph
Effectiveness, Immunogenicity and Harms of Additional SARS-CoV-2 Vaccine Doses in Kidney Transplant Recipients: A Systematic Review
title Effectiveness, Immunogenicity and Harms of Additional SARS-CoV-2 Vaccine Doses in Kidney Transplant Recipients: A Systematic Review
title_full Effectiveness, Immunogenicity and Harms of Additional SARS-CoV-2 Vaccine Doses in Kidney Transplant Recipients: A Systematic Review
title_fullStr Effectiveness, Immunogenicity and Harms of Additional SARS-CoV-2 Vaccine Doses in Kidney Transplant Recipients: A Systematic Review
title_full_unstemmed Effectiveness, Immunogenicity and Harms of Additional SARS-CoV-2 Vaccine Doses in Kidney Transplant Recipients: A Systematic Review
title_short Effectiveness, Immunogenicity and Harms of Additional SARS-CoV-2 Vaccine Doses in Kidney Transplant Recipients: A Systematic Review
title_sort effectiveness, immunogenicity and harms of additional sars-cov-2 vaccine doses in kidney transplant recipients: a systematic review
topic Systematic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141039/
https://www.ncbi.nlm.nih.gov/pubmed/37112775
http://dx.doi.org/10.3390/vaccines11040863
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