HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Comparative Effectiveness of BNT162b2 and mRNA-1273 Vaccines Against COVID-19 Infection Among Patients With Systemic Autoimmune Rheumatic Diseases on Immunomodulatory Medications.

AbstractOBJECTIVE:
To compare the effectiveness of mRNA vaccines (BNT162b2 vs mRNA-1273) against coronavirus disease 2019 (COVID-19) infection among patients with systemic autoimmune rheumatic diseases (SARDs) on immunomodulatory medications.
METHODS:
We identified patients with SARDs being treated with disease-modifying antirheumatic drugs (DMARDs) and/or glucocorticoids in the Mass General Brigham healthcare system who received either BNT162b2 or mRNA-1273 as their initial vaccine series. Patients were followed until positive SARS-CoV-2 test, death, or February 22, 2022. We compared the risk of breakthrough infection between BNT162b2 and mRNA-1273 vaccine recipients using time-stratified, overlap propensity score (PS)-weighted Cox proportional hazard models.
RESULTS:
We identified 9838 patients with SARDs who received BNT162b2 or mRNA-1273. Demographic and clinical characteristics were similar in both groups after overlap weighting: mean age 61 years, 75% female, 52% with rheumatoid arthritis, 74% receiving conventional synthetic DMARDs, and 43% receiving biologic DMARDs. Of 5516 BNT162b2 and 4322 mRNA-1273 recipients, 446 and 329 had a breakthrough infection, respectively. The corresponding time-stratified PS-weighted rate difference of breakthrough infection was 0.71 (95% CI -0.70 to 2.12) per 1000 person-months with a weighted hazard ratio (HR) of 1.12 (95% CI 0.90 to 1.39). When follow-up was censored prior to the Omicron wave, there was a trend toward higher breakthrough risk with BNT162b2 vs mRNA-1273 (weighted HR 1.34, 95% CI 0.91 to 1.98).
CONCLUSION:
Among patients with SARDs, the risk of breakthrough COVID-19 infection is similar after receiving either BNT162b2 or mRNA-1273. Patients with SARDs initiating the vaccine series should be encouraged to receive whichever mRNA vaccine is available.
AuthorsClaire E Cook, Naomi J Patel, Xiaoqing Fu, Xiaosong Wang, Yumeko Kawano, Kathleen M M Vanni, Grace Qian, Emily Banasiak, Emily Kowalski, Hyon K Choi, Yuqing Zhang, Jeffrey A Sparks, Zachary S Wallace
JournalThe Journal of rheumatology (J Rheumatol) Vol. 50 Issue 5 Pg. 697-703 (05 2023) ISSN: 0315-162X [Print] Canada
PMID36642428 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2023 by the Journal of Rheumatology.
Chemical References
  • BNT162 Vaccine
  • 2019-nCoV Vaccine mRNA-1273
  • COVID-19 Vaccines
  • mRNA Vaccines
  • Antirheumatic Agents
Topics
  • Humans
  • Female
  • Middle Aged
  • Male
  • BNT162 Vaccine
  • 2019-nCoV Vaccine mRNA-1273
  • COVID-19
  • COVID-19 Vaccines
  • SARS-CoV-2
  • mRNA Vaccines
  • Antirheumatic Agents
  • Arthritis, Rheumatoid

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: