Use of infliximab and other biologics in Behçet disease
1Department of Clinical Immunology and Allergy, Royal North Shore Hospital, Sydney, New South Wales, Australia.
Insights
Behçet disease, a rare vasculitis, can affect the nervous system. Tumor necrosis factor antagonists, like infliximab, show promise for treating neuro-Behçet disease, improving outcomes for affected young men.
Area of Science:
- Immunology
- Neurology
- Rheumatology
Background:
- Behçet disease is a rare multisystem vasculitis.
- Characterized by recurrent oral ulcers and other systemic manifestations.
- Neurological involvement, or neuro-Behçet disease, is a severe complication.
Observation:
- Neuro-Behçet disease typically affects young men aged 20-40.
- This condition is associated with significant long-term morbidity and mortality.
- Case literature suggests potential treatment avenues.
Findings:
- Tumor necrosis factor (TNF) antagonists are a potential therapeutic option.
- Infliximab, a specific TNF antagonist, has demonstrated efficacy in case studies.
- Evidence supports its use in managing neuro-Behçet disease.
Implications:
- Targeted immunosuppression with TNF antagonists may alter disease course.
- Infliximab offers a treatment strategy for severe neuro-Behçet disease.
- Further research could solidify the role of biologics in managing this rare vasculitis.
Abstract:
Behçet disease is a multisystem vasculitis characterised by recurrent oral ulceration in conjunction with other manifestations. Neurological involvement or neuro-Behçet disease is not common, but typically affects young men at its onset between the ages of 20 and 40 with significant long-term morbidity and mortality. There is substantial case literature to support the use of tumour necrosis factor antagonists, notably infliximab, in the treatment of neuro-Behçet disease.
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