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Influence of vitamin D supplementation on SARS-CoV-2 vaccine efficacy and immunogenicity
David A Jolliffe; Giulia Vivaldi; Emma S Chambers; Weigang Cai; Wenhao Li; Sian E Faustini; Joseph M Gibbons; Corinna Pade; Alex Richter; Aine McKnight; Adrian R Martineau.
Affiliation
  • David A Jolliffe; Queen Mary University of London
  • Giulia Vivaldi; Queen Mary University of London
  • Emma S Chambers; Queen Mary University of London
  • Weigang Cai; Queen Mary University of London
  • Wenhao Li; Queen Mary University of London
  • Sian E Faustini; University of Birmingham
  • Joseph M Gibbons; Barts and The London School of Medicine and Dentistry Blizard Institute
  • Corinna Pade; Queen Mary University of London
  • Alex Richter; University of Birminghan
  • Aine McKnight; Barts and The London School of Medicine and Dentistry Blizard Institute
  • Adrian R Martineau; Queen Mary University of London
Preprint de En | PREPRINT-MEDRXIV | ID: ppmedrxiv-22277678
ABSTRACT
SUMMARYO_ST_ABSBackground & AimsC_ST_ABSVitamin D deficiency has been reported to associate with impaired development of antigen-specific responses following vaccination. We aimed to determine whether vitamin D supplements might boost immunogenicity and efficacy of SARS-CoV-2 vaccination. MethodsWe conducted three sub-studies nested within the CORONAVIT randomised controlled trial, which investigated effects of offering vitamin D supplements at a dose of 800 IU/day or 3200 IU/day vs. no offer on risk of acute respiratory infections, including COVID-19, in UK adults with circulating 25-hydroxyvitamin D concentrations <75 nmol/L. Sub-study 1 (n=2808) investigated effects of vitamin D supplementation on risk of breakthrough SARS-CoV-2 infection following two doses of SARS-CoV-2 vaccine. Sub-study 2 (n=1853) investigated effects of vitamin D supplementation on titres of combined IgG, IgA and IgM (IgGAM) anti-Spike antibodies in eluates of dried blood spots collected after SARS-CoV-2 vaccination. Sub-study 3 (n=100) investigated effects of vitamin D supplementation on neutralising antibody and cellular responses in venous blood samples collected after SARS-CoV-2 vaccination. Results1945/2808 (69.3%) sub-study 1 participants received two doses of ChAdOx1 nCoV-19 (Oxford-AstraZeneca); the remainder received two doses of BNT162b2 (Pfizer). Vitamin D supplementation did not influence risk of breakthrough SARS-CoV-2 infection (800 IU/day vs. no offer adjusted hazard ratio 1.28, 95% CI 0.89 to 1.84; 3200 IU/day vs. no offer 1.17, 0.81 to 1.70). Neither did it influence IgGAM anti-Spike titres, neutralising antibody titres or IFN-{gamma} concentrations in supernatants of S peptide-stimulated whole blood. ConclusionsAmong adults with sub-optimal baseline vitamin D status, vitamin D replacement at a dose of 800 or 3200 IU/day did not influence protective efficacy or immunogenicity of SARS-CoV-2 vaccination. Clinical Trial RegistrationClinicalTrials.gov NCT04579640.
Licence
cc_by_nc_nd
Texte intégral: 1 Collection: 09-preprints Base de données: PREPRINT-MEDRXIV Type d'étude: Experimental_studies / Prognostic_studies / Rct Langue: En Année: 2022 Type de document: Preprint
Texte intégral: 1 Collection: 09-preprints Base de données: PREPRINT-MEDRXIV Type d'étude: Experimental_studies / Prognostic_studies / Rct Langue: En Année: 2022 Type de document: Preprint