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Updated: Apr 27, 2026

Determination of the Relative Potency of an Anti-TNF Monoclonal Antibody mAb by Neutralizing TNF Using an In Vitro Bioanalytical Method
Published on: September 16, 2017
The use of non-TNF targeted biologics in Behçet's disease: real-life data from the International AIDA Network
Gizem Sevik1, Giuseppe Lopalco2, Florenzo Iannone2
1Department of Internal Medicine, Division of Rheumatology, Faculty of Medicine, Marmara University, Istanbul, Turkey.
Objectives:
Refractory manifestations of Behçet's disease (BD) are commonly treated with TNF-α inhibitors; however, a subset of patients do not respond or are intolerant, prompting the need for alternative therapies. This study aimed to assess the real-life use, efficacy, and safety of non-TNF targeted biologic agents in BD.
Methods:
Data were retrieved from the International AutoInflammatory Disease Alliance (AIDA) Network Registry for BD. Patients who received any biologic agent other than TNF-α inhibitors at any point during follow-up were included in the study. Clinical and demographic characteristics, prior treatments, and treatment responses at the 3-, 6- and 12-month follow-ups were collected.
Results:
In total, 65 patients (36 female/29 male) with a mean age of 45.8 ± 13.3 years were included in the sample population for this study. Anakinra was the most frequently used agent (n = 31), with 34.7% of patients with mucocutaneous, 73.3% with musculoskeletal, and 77.7% with ocular involvement showing a partial or complete response. Canakinumab (n = 11) was effective in mucocutaneous, musculoskeletal and ocular involvement, including in some patients previously unresponsive to anakinra. Tocilizumab (n = 15) showed favourable outcomes in ocular and neurological involvement (a complete response in 5 of 6 patients), while 40% experienced worsening or no response in mucocutaneous manifestations. Secukinumab and ixekizumab were effective in patients with mucocutaneous-articular phenotypes, especially those with axial SpA. Ustekinumab (n = 3) and rituximab (n = 5) also demonstrated clinical improvement in selected refractory cases. No new major safety concerns were reported across the treatment groups.
Conclusion:
Biologics targeting IL-1, IL-6, IL-17 and the IL-12/23 pathways may offer therapeutic alternatives in BD patients unresponsive to TNF-α inhibitors. The treatment efficacy varied across phenotypes, highlighting the need for individualized treatment decisions.
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