Risk of Autoimmune Diseases Associated with Biologic Agents Targeting Type 2 Immunity: An Observational Study Using a Claims Database
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Objective.
Biologic agents targeting type 2 immunity (anti-type 2 agents) have been implicated in the risk of autoimmune diseases. This study aimed to assess the association between anti-type 2 agents and the risk of developing autoimmune diseases.
Methods.
This retrospective cohort, nested case-control study utilized a large claims database in Japan. Patients diagnosed with bronchial asthma, atopic dermatitis, chronic urticaria, or eosinophilic chronic rhinosinusitis after April 2018 were included. The exposures of interest were anti-interleukin (IL)-5, anti-IL-4, and anti-IgE agents. The study outcomes included 11 autoimmune diseases and their composite. The risk of developing autoimmune diseases was assessed using two statistical models: nested case-control analysis (NCC) and time-dependent Cox proportional hazard model (tCox).
Results.
A total of 886,908 patients were included, with a median age of 42 years (interquartile range: 32.0–52.0). The use of the anti-IL-5 agent and anti-IgE agent showed consistent associations with the composite outcome: adjusted relative risk (RR) 2.50 (95% confidence interval [CI] 1.35, 4.64) in NCC and 3.02 (1.86, 4.90) in tCox, and 2.25 (1.37, 3.67) in NCC and 2.33 (1.61, 3.39) in tCox, respectively. Regarding individual outcomes, rheumatoid arthritis, systemic lupus erythematosus, and anti-neutrophil cytoplasmic antibody-associated vasculitis were associated with the use of anti-IL-5 agents. In patients with atopic dermatitis, anti-IL-4 agents appear to reduce the risk of psoriasis.
Conclusion.
Although causal interpretation is limited, it provides valuable insights into the association between anti-type 2 agents and autoimmune diseases in real-world clinical practice.
Significance and Innovations
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Anti-IL-5 and anti-IgE agents are associated with an increased risk of autoimmune diseases.
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Anti-IL-4 agents show no remarkable link to autoimmune diseases but reduce psoriasis risk in atopic dermatitis.
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This study explores the effects of anti-type 2 agents and autoimmune diseases in real-world settings.