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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.
Afiliação
  • Smith RM; Department of Medicine, University of Cambridge, Cambridge, UK.
  • Cooper DJ; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Doffinger R; Department of Renal Medicine, Addenbrooke's Hospital, Hills Road, Box 118, Cambridge, CB2 0QQ, UK.
  • Stacey H; Department of Medicine, University of Cambridge, Cambridge, UK.
  • Al-Mohammad A; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Goodfellow I; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Baker S; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Lear S; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Hosmilo M; Division of Virology, Department of Pathology, University of Cambridge, Cambridge, UK.
  • Pritchard N; Department of Medicine, University of Cambridge, Cambridge, UK.
  • Torpey N; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Jayne D; Division of Virology, Department of Pathology, University of Cambridge, Cambridge, UK.
  • Yiu V; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Chalisey A; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Lee J; Department of Medicine, University of Cambridge, Cambridge, UK.
  • Vilnar E; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
  • Cheung CK; West Suffolk Hospital NHS Foundation Trust, Bury St Edmunds, UK.
  • Jones RB; Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
BMC Nephrol ; 23(1): 199, 2022 05 31.
Article em En | MEDLINE | ID: mdl-35641961
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Vacinas Virais / COVID-19 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doenças Autoimunes / Vacinas Virais / COVID-19 Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article