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Comparative Effectiveness of Abatacept Versus Adalimumab in Shared Epitope Positive and Negative Patients With Rheumatoid Arthritis

Lookup NU author(s): Professor John IsaacsORCiD

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

© 2025 The Author(s). Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology. Objective: The effect of the shared epitope (SE) and valine at position 11 (Val11) of HLA–DRB1 on the activation of CD4+ T cells is expected to be diminished by abatacept, a costimulation blocker. However, published evidence on the value of genetic stratification for abatacept treatment is conflicting. We aimed to compare the difference in effectiveness of abatacept and adalimumab in patients carrying the SE (or Val11). Methods: The Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate is a nationwide observational cohort study recruiting patients from 53 centers across the United Kingdom before the initiation of biologic treatment and following them up prospectively for 12 months. Three hundred forty-two patients starting either abatacept or adalimumab were eligible for this analysis. Serum drug levels for abatacept, adalimumab, and methotrexate were determined at multiple time points. Multivariate modeling integrating demographic, clinical, and pharmacological variables was used to test for associations between the number of copies of the SE or Val11 and response to treatment (EULAR response; Disease Activity Score in 28 joints [DAS28] remission; change in DAS28). Differential effectiveness between drugs and genetic markers was assessed by the significance of their interaction term. Results: There was no difference in the efficacy of abatacept versus adalimumab. We found weak evidence for an independent association of genetic markers with response to treatment (Val11 with EULAR response: P = 0.02), but there was no significant difference in this effect between drugs. Conclusion: We found no evidence that HLA typing is clinically useful to support prescription decisions for these two drugs. (Figure presented.).


Publication metadata

Author(s): Yap CF, Nair N, Sharma SD, Bowes J, Ariff ABM, Morgan AW, Isaacs JD, Wilson AG, Hyrich KL, Verstappen S, Bluett J, Morris AP, Barton A, Plant D, Viatte S

Publication type: Article

Publication status: Published

Journal: Arthritis and Rheumatology

Year: 2025

Pages: Epub ahead of print

Online publication date: 26/06/2025

Acceptance date: 10/06/2025

Date deposited: 06/10/2025

ISSN (print): 2326-5191

ISSN (electronic): 2326-5205

Publisher: John Wiley and Sons Inc.

URL: https://doi.org/10.1002/art.43298

DOI: 10.1002/art.43298

PubMed id: 40567118


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Funding

Funder referenceFunder name
Bristol Myers Squibb
Leeds Biomedical Research Centre. Grant Number: NIHR203331
NIHR Manchester Biomedical Research Centre. Grant Number: NIHR203308
NIHR Newcastle Biomedical Research Centre
Versus Arthritis. Grant Number: 21754

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