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SARS-COV-2 vaccine responses in renal patient populations
BACKGROUND: Dialysis patients and immunosuppressed renal patients are at increased risk of COVID-19 and were excluded from vaccine trials. We conducted a prospective multicentre study to assess SARS-CoV-2 vaccine antibody responses in dialysis patients and renal transplant recipients, and patients r...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153874/ https://www.ncbi.nlm.nih.gov/pubmed/35641961 http://dx.doi.org/10.1186/s12882-022-02792-w |
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author | Smith, Rona M. Cooper, Daniel J. Doffinger, Rainer Stacey, Hannah Al-Mohammad, Abdulrahman Goodfellow, Ian Baker, Stephen Lear, Sara Hosmilo, Myra Pritchard, Nicholas Torpey, Nicholas Jayne, David Yiu, Vivien Chalisey, Anil Lee, Jacinta Vilnar, Enric Cheung, Chee Kay Jones, Rachel B. |
author_facet | Smith, Rona M. Cooper, Daniel J. Doffinger, Rainer Stacey, Hannah Al-Mohammad, Abdulrahman Goodfellow, Ian Baker, Stephen Lear, Sara Hosmilo, Myra Pritchard, Nicholas Torpey, Nicholas Jayne, David Yiu, Vivien Chalisey, Anil Lee, Jacinta Vilnar, Enric Cheung, Chee Kay Jones, Rachel B. |
author_sort | Smith, Rona M. |
collection | PubMed |
description | BACKGROUND: Dialysis patients and immunosuppressed renal patients are at increased risk of COVID-19 and were excluded from vaccine trials. We conducted a prospective multicentre study to assess SARS-CoV-2 vaccine antibody responses in dialysis patients and renal transplant recipients, and patients receiving immunosuppression for autoimmune disease. METHODS: Patients were recruited from three UK centres (ethics:20/EM/0180) and compared to healthy controls (ethics:17/EE/0025). SARS-CoV-2 IgG antibodies to spike protein were measured using a multiplex Luminex assay, after first and second doses of Pfizer BioNTech BNT162b2(Pfizer) or Oxford-AstraZeneca ChAdOx1nCoV-19(AZ) vaccine. RESULTS: Six hundred ninety-two patients were included (260 dialysis, 209 transplant, 223 autoimmune disease (prior rituximab 128(57%)) and 144 healthy controls. 299(43%) patients received Pfizer vaccine and 379(55%) received AZ. Following two vaccine doses, positive responses occurred in 96% dialysis, 52% transplant, 70% autoimmune patients and 100% of healthy controls. In dialysis patients, higher antibody responses were observed with the Pfizer vaccination. Predictors of poor antibody response were triple immunosuppression (adjusted odds ratio [aOR]0.016;95%CI0.002–0.13;p < 0.001) and mycophenolate mofetil (MMF) (aOR0.2;95%CI 0.1–0.42;p < 0.001) in transplant patients; rituximab within 12 months in autoimmune patients (aOR0.29;95%CI 0.008–0.096;p < 0.001) and patients receiving immunosuppression with eGFR 15-29 ml/min (aOR0.031;95%CI 0.11–0.84;p = 0.021). Lower antibody responses were associated with a higher chance of a breakthrough infection. CONCLUSIONS: Amongst dialysis, kidney transplant and autoimmune populations SARS-CoV-2 vaccine antibody responses are reduced compared to healthy controls. A reduced response to vaccination was associated with rituximab, MMF, triple immunosuppression CKD stage 4. Vaccine responses increased after the second dose, suggesting low-responder groups should be prioritised for repeated vaccination. Greater antibody responses were observed with the mRNA Pfizer vaccine compared to adenovirus AZ vaccine in dialysis patients suggesting that Pfizer SARS-CoV-2 vaccine should be the preferred vaccine choice in this sub-group. |
format | Online Article Text |
id | pubmed-9153874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91538742022-06-02 SARS-COV-2 vaccine responses in renal patient populations Smith, Rona M. Cooper, Daniel J. Doffinger, Rainer Stacey, Hannah Al-Mohammad, Abdulrahman Goodfellow, Ian Baker, Stephen Lear, Sara Hosmilo, Myra Pritchard, Nicholas Torpey, Nicholas Jayne, David Yiu, Vivien Chalisey, Anil Lee, Jacinta Vilnar, Enric Cheung, Chee Kay Jones, Rachel B. BMC Nephrol Research BACKGROUND: Dialysis patients and immunosuppressed renal patients are at increased risk of COVID-19 and were excluded from vaccine trials. We conducted a prospective multicentre study to assess SARS-CoV-2 vaccine antibody responses in dialysis patients and renal transplant recipients, and patients receiving immunosuppression for autoimmune disease. METHODS: Patients were recruited from three UK centres (ethics:20/EM/0180) and compared to healthy controls (ethics:17/EE/0025). SARS-CoV-2 IgG antibodies to spike protein were measured using a multiplex Luminex assay, after first and second doses of Pfizer BioNTech BNT162b2(Pfizer) or Oxford-AstraZeneca ChAdOx1nCoV-19(AZ) vaccine. RESULTS: Six hundred ninety-two patients were included (260 dialysis, 209 transplant, 223 autoimmune disease (prior rituximab 128(57%)) and 144 healthy controls. 299(43%) patients received Pfizer vaccine and 379(55%) received AZ. Following two vaccine doses, positive responses occurred in 96% dialysis, 52% transplant, 70% autoimmune patients and 100% of healthy controls. In dialysis patients, higher antibody responses were observed with the Pfizer vaccination. Predictors of poor antibody response were triple immunosuppression (adjusted odds ratio [aOR]0.016;95%CI0.002–0.13;p < 0.001) and mycophenolate mofetil (MMF) (aOR0.2;95%CI 0.1–0.42;p < 0.001) in transplant patients; rituximab within 12 months in autoimmune patients (aOR0.29;95%CI 0.008–0.096;p < 0.001) and patients receiving immunosuppression with eGFR 15-29 ml/min (aOR0.031;95%CI 0.11–0.84;p = 0.021). Lower antibody responses were associated with a higher chance of a breakthrough infection. CONCLUSIONS: Amongst dialysis, kidney transplant and autoimmune populations SARS-CoV-2 vaccine antibody responses are reduced compared to healthy controls. A reduced response to vaccination was associated with rituximab, MMF, triple immunosuppression CKD stage 4. Vaccine responses increased after the second dose, suggesting low-responder groups should be prioritised for repeated vaccination. Greater antibody responses were observed with the mRNA Pfizer vaccine compared to adenovirus AZ vaccine in dialysis patients suggesting that Pfizer SARS-CoV-2 vaccine should be the preferred vaccine choice in this sub-group. BioMed Central 2022-05-31 /pmc/articles/PMC9153874/ /pubmed/35641961 http://dx.doi.org/10.1186/s12882-022-02792-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Smith, Rona M. Cooper, Daniel J. Doffinger, Rainer Stacey, Hannah Al-Mohammad, Abdulrahman Goodfellow, Ian Baker, Stephen Lear, Sara Hosmilo, Myra Pritchard, Nicholas Torpey, Nicholas Jayne, David Yiu, Vivien Chalisey, Anil Lee, Jacinta Vilnar, Enric Cheung, Chee Kay Jones, Rachel B. SARS-COV-2 vaccine responses in renal patient populations |
title | SARS-COV-2 vaccine responses in renal patient populations |
title_full | SARS-COV-2 vaccine responses in renal patient populations |
title_fullStr | SARS-COV-2 vaccine responses in renal patient populations |
title_full_unstemmed | SARS-COV-2 vaccine responses in renal patient populations |
title_short | SARS-COV-2 vaccine responses in renal patient populations |
title_sort | sars-cov-2 vaccine responses in renal patient populations |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9153874/ https://www.ncbi.nlm.nih.gov/pubmed/35641961 http://dx.doi.org/10.1186/s12882-022-02792-w |
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