SARS-COV-2 vaccine responses in renal patient populations.
cam.issuedOnline | 2022-05-31 | |
dc.contributor.author | Smith, Rona M | |
dc.contributor.author | Cooper, Daniel J | |
dc.contributor.author | Doffinger, Rainer | |
dc.contributor.author | Stacey, Hannah | |
dc.contributor.author | Al-Mohammad, Abdulrahman | |
dc.contributor.author | Goodfellow, Ian | |
dc.contributor.author | Baker, Stephen | |
dc.contributor.author | Lear, Sara | |
dc.contributor.author | Hosmilo, Myra | |
dc.contributor.author | Pritchard, Nicholas | |
dc.contributor.author | Torpey, Nicholas | |
dc.contributor.author | Jayne, David | |
dc.contributor.author | Yiu, Vivien | |
dc.contributor.author | Chalisey, Anil | |
dc.contributor.author | Lee, Jacinta | |
dc.contributor.author | Vilnar, Enric | |
dc.contributor.author | Cheung, Chee Kay | |
dc.contributor.author | Jones, Rachel B | |
dc.contributor.orcid | Cooper, Daniel [0000-0002-3643-7605] | |
dc.contributor.orcid | Baker, Stephen [0000-0003-1308-5755] | |
dc.contributor.orcid | Jayne, David [0000-0002-1712-0637] | |
dc.date.accessioned | 2022-06-07T08:11:47Z | |
dc.date.available | 2022-06-07T08:11:47Z | |
dc.date.issued | 2022-05-31 | |
dc.date.submitted | 2021-12-24 | |
dc.date.updated | 2022-06-07T08:11:46Z | |
dc.description.abstract | 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. | |
dc.identifier.doi | 10.17863/CAM.85172 | |
dc.identifier.eissn | 1471-2369 | |
dc.identifier.issn | 1471-2369 | |
dc.identifier.other | s12882-022-02792-w | |
dc.identifier.other | 2792 | |
dc.identifier.uri | https://www.repository.cam.ac.uk/handle/1810/337763 | |
dc.language | en | |
dc.language.iso | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.publisher.url | http://dx.doi.org/10.1186/s12882-022-02792-w | |
dc.subject | Antibody | |
dc.subject | Autoimmune | |
dc.subject | Dialysis | |
dc.subject | Immunosuppression | |
dc.subject | Mycophenolate | |
dc.subject | Rituximab | |
dc.subject | SARS-CoV-2 | |
dc.subject | Transplant | |
dc.subject | Vaccine | |
dc.subject | Autoimmune Diseases | |
dc.subject | BNT162 Vaccine | |
dc.subject | COVID-19 | |
dc.subject | COVID-19 Vaccines | |
dc.subject | Humans | |
dc.subject | Mycophenolic Acid | |
dc.subject | Renal Dialysis | |
dc.subject | Rituximab | |
dc.subject | SARS-CoV-2 | |
dc.subject | Viral Vaccines | |
dc.title | SARS-COV-2 vaccine responses in renal patient populations. | |
dc.type | Article | |
dcterms.dateAccepted | 2022-04-11 | |
prism.issueIdentifier | 1 | |
prism.publicationName | BMC Nephrol | |
prism.volume | 23 | |
pubs.funder-project-id | Wellcome Trust (207498/Z/17/Z) | |
rioxxterms.licenseref.uri | http://creativecommons.org/licenses/by/4.0/ | |
rioxxterms.version | VoR | |
rioxxterms.versionofrecord | 10.1186/s12882-022-02792-w |
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