BNT162b2 versus mRNA-1273 Third Dose COVID-19 Vaccine in Patients with CKD and Maintenance Dialysis Patients

Author:

Yau Kevin123ORCID,Tam Paul4ORCID,Chan Christopher T.23ORCID,Hu Queenie5,Qi Freda5ORCID,Abe Kento T.56,Kurtesi Alexandra5ORCID,Jiang Yidi7ORCID,Estrada-Codecido Jose1ORCID,Brown Tyler1,Liu Lisa1,Siwakoti Aswani1,Leis Jerome A.38ORCID,Levin Adeera9,Oliver Matthew J.1310ORCID,Colwill Karen5ORCID,Gingras Anne-Claude56ORCID,Hladunewich Michelle A.1310ORCID

Affiliation:

1. Division of Nephrology, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada

2. Division of Nephrology, Department of Medicine, University Health Network, Toronto, Ontario, Canada

3. Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada

4. Division of Nephrology, Department of Medicine, Scarborough Health Network, Toronto, Ontario, Canada

5. Lunenfeld-Tanenbaum Research Institute at Mount Sinai Hospital, Sinai Health System, Toronto, Ontario, Canada

6. Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada

7. Clinical Trial Support, Sunnybrook Research Institute, Toronto, Ontario, Canada

8. Division of Infectious Diseases, Department of Medicine, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada

9. British Columbia Provincial Renal Agency, Vancouver, British Columbia, Canada

10. Ontario Renal Network, Ontario Health, Toronto, Ontario, Canada

Abstract

Background There is a lack of randomized controlled trial data regarding differences in immunogenicity of varying coronavirus disease 2019 (COVID-19) mRNA vaccine regimens in CKD populations. Methods We conducted a randomized controlled trial at three kidney centers in Toronto, Ontario, Canada, evaluating the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibody response after third dose vaccination. Participants (n=273) with CKD not on dialysis or receiving dialysis were randomized 1:1 to third dose 30-µg BNT162b2 (Pfizer-BioNTech) or 100-µg mRNA-1273 (Moderna). The primary outcome of this study was SARS-CoV-2 IgG-binding antibodies to the receptor-binding domain (anti-RBD). Spike protein (antispike), nucleocapsid protein, and vaccine reactogenicity were also evaluated. Serology was measured before third dose and 1, 3, and 6 months after third dose. A subset of participants (n=100) were randomly selected to assess viral pseudovirus neutralization against wild-type D614G, B.1.617.2 (Delta), and B.1.1.529 (Omicron BA.1). Results Among 273 participants randomized, 94% were receiving maintenance dialysis and 59% received BNT162b2 for initial two dose COVID-19 vaccination. Third dose of mRNA-1273 was associated with higher mean anti-RBD levels (1871 binding antibody units [BAU]/ml; 95% confidence interval [CI], 829 to 2988) over a 6-month period in comparison with third dose BNT162b2 (1332 BAU/ml; 95% CI, 367 to 2402) with a difference of 539 BAU/ml (95% CI, 139 to 910; P = 0.009). Neither antispike levels nor neutralizing antibodies to wild-type, Delta, and Omicron BA.1 pseudoviruses were statistically different. COVID-19 infection occurred in 10% of participants: 15 (11%) receiving mRNA-1273 and 11 (8%) receiving BNT162b2. Third dose BNT162b2 was not associated with a significant different risk for COVID-19 in comparison with mRNA-1273 (hazard ratio, 0.78; 95% CI, 0.27 to 2.2; P = 0.63). Conclusions In patients with CKD, third dose COVID-19 mRNA vaccination with mRNA-1273 elicited higher SARS-CoV-2 anti-RBD levels in comparison with BNT162b2 over a 6-month period. Clinical Trial registry name and registration number COVID-19 Vaccine Boosters in Patients With CKD (BOOST KIDNEY), NCT05022329.

Funder

COVID-19 Immunity Task Force

Oreopoulos/Baxter Home Dialysis Grant

Canadian Institutes of Health Research

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Transplantation,Nephrology,Critical Care and Intensive Care Medicine,Epidemiology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. COVID-19 Vaccination in Patients Receiving Dialysis;Clinical Journal of the American Society of Nephrology;2023-12-19

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