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Efficacy of COVID-19 vaccines in patients taking immunosuppressants.
Shen, Chen; Risk, Malcolm; Schiopu, Elena; Hayek, Salim S; Xie, Tiankai; Holevinski, Lynn; Akin, Cem; Freed, Gary; Zhao, Lili.
  • Shen C; Department of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA.
  • Risk M; Department of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA.
  • Schiopu E; Department of Rheumatology, University of Michigan Michigan Medicine, Ann Arbor, Michigan, USA.
  • Hayek SS; Department of Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Xie T; Department of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA.
  • Holevinski L; Data Office for Clinical and Translational Research, University of Michigan Medical School, Ann Arbor, Michigan, USA.
  • Akin C; Division of Allergy, University of Michigan, Ann Arbor, Michigan, USA.
  • Freed G; Department of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA.
  • Zhao L; Department of Biostatistics, University of Michigan, Ann Arbor, Michigan, USA zhaolili@med.umich.edu.
Ann Rheum Dis ; 81(6): 875-880, 2022 06.
Article in English | MEDLINE | ID: covidwho-1701139
ABSTRACT

OBJECTIVES:

We intended to assess the effectiveness of all three US Food and Drug Administration approved COVID-19 vaccines at preventing SARS-CoV-2 infection and COVID-19 hospitalisation in a large cohort of individuals on immunosuppressants for a diverse range of conditions.

METHODS:

We studied the effectiveness of BNT162b2 (Pfizer-BioNTech), mRNA-1273 (Moderna) and Ad26.COV2.S (Johnson & Johnson-Janssen) vaccines among individuals who take immunosuppressants (including disease-modifying antirheumatic drugs and glucocorticoids) by comparing vaccinated (n=97688) and unvaccinated (n=42094) individuals in the Michigan Medicine healthcare system from 1 January to 7 December 2021, using Cox proportional hazards modelling with time-varying covariates.

RESULTS:

Among vaccinated and unvaccinated individuals, taking immunosuppressants increased the risk of SARS-CoV-2 infection (adjusted HR (aHR)=2.17, 95% CI 1.69 to 2.79 for fully vaccinated and aHR=1.40, 95% CI 1.07 to 1.83 for unvaccinated). Among individuals taking immunosuppressants, we found (1) vaccination reduced the risk of SARS-CoV-2 infection (aHR=0.55, 95% CI 0.39 to 0.78); (2) the BNT162b2 and mRNA-1273 vaccines were highly effective at reducing the risk of SARS-CoV-2 infection (n=2046, aHR=0.59, 95% CI 0.38 to 0.91 for BNT162b2; n=2064, aHR=0.52, 95% CI 0.33 to 0.82 for mRNA-1273); (3) with a smaller sample size (n=173), Ad26.COV2.S vaccine protection did not reach statistical significance (aHR=0.34, 95% CI 0.09 to 1.30, p=0.17); and (4) receiving a booster dose reduced the risk of SARS-CoV-2 infection (aHR=0.42, 95% CI 0.24 to 0.76).

CONCLUSIONS:

The mRNA-1273 and BNT162b2 vaccines are effective in individuals who take immunosuppressants. However, individuals who are vaccinated but on immunosuppressants are still at higher risk of SARS-CoV-2 infection and COVID-19 hospitalisation than the broader vaccinated population. Booster doses are effective and crucially important for individuals on immunosuppressants.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Ann Rheum Dis Year: 2022 Document Type: Article Affiliation country: Annrheumdis-2021-222045

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Vaccines / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Ann Rheum Dis Year: 2022 Document Type: Article Affiliation country: Annrheumdis-2021-222045