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Review of anti-TL1A therapies for hidradenitis suppurativa with no reported outcomes or safety data

Review of anti-TL1A therapies for hidradenitis suppurativa with no reported outcomes or safety data
Photo by Brett Jordan / Unsplash
Key Takeaway
Note that this review of anti-TL1A therapies lacks reported outcomes or safety data.

This publication is a narrative review focusing on the potential role of anti-TL1A therapies, including tulisokibart, in the management of hidradenitis suppurativa. The scope of the article is limited to discussing this specific mechanism of action within the context of the disease. No quantitative data regarding patient numbers or specific trial results are provided within the source text.

The authors note that critical information regarding the study population, sample size, and setting was not reported. Furthermore, primary and secondary outcomes, as well as follow-up duration, are absent from the provided data. Safety profiles, including adverse events and tolerability, are similarly not reported in this review.

Given the lack of reported outcomes and safety data, the practice relevance of this specific review is currently unclear. Clinicians should interpret these findings with caution, recognizing that the source does not provide the numerical evidence required to support specific clinical decisions regarding tulisokibart or anti-TL1A therapies at this time.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
Hidradenitis suppurativa (HS) is a chronic inflammatory disorder that presents with both cutaneous manifestations and extracutaneous comorbidities. Current treatment options include antibiotics and biologics; however, treatment failure is common and often surgical intervention is required for acceptable control. Anti-TL1A therapies have recently gained attention in HS treatment due to their ability to inhibit the TL1A/DR3 axis, a key signaling pathway driving immune cell activity and fibrosis. Participant recruitment for the phase 2b trial (NCT06956235) assessing the efficacy of anti-TL1A therapy tulisokibart in moderate-to severe HS was reported on 1 December, 2025 to be completed. This review aims to explore the potential links between the TL1A and HS by synthesizing immune mechanisms of HS pathogenesis with existing data of the TL1A/DR3 axis in immune pathways. A discussion highlighting the potential for anti-TL1A therapies as a class that simultaneously addresses fibrosis and comorbidities of HS is also presented, and future directions to address knowledge gaps are also proposed.
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