# JAK Inhibitor and Crohn’s Disease

**Authors:** Mengyan Xu, Shi Wang, Sanping Xu, Rui Gong

PMC · DOI: 10.3390/biomedicines13061325 · 2025-05-29

## TL;DR

This paper reviews the use of JAK inhibitors for treating Crohn’s disease, highlighting their benefits and risks based on clinical trial outcomes.

## Contribution

The paper provides a systematic review of JAK inhibitors' efficacy and safety in Crohn’s disease, comparing different drugs and their clinical trial results.

## Key findings

- Tofacitinib shows limited efficacy in managing Crohn’s disease.
- Upadacitinib achieves notable clinical remission in both induction and maintenance phases.
- JAK inhibitors raise long-term safety concerns like infections and malignancy risks.

## Abstract

Crohn’s disease is a chronic inflammatory granulomatous disease of the gastrointestinal tract. The global incidence and prevalence of Crohn’s disease have significantly increased, largely due to genetic susceptibility, environmental changes, and advancements in diagnostic technology. In recent years, the pharmacologic treatment of Crohn’s disease has been rapidly changing, and although biologics have improved the prognosis of patients to a certain extent, they still have certain limitations. Oral small molecule drugs like JAK inhibitors have become a research hotspot because of their advantages of targeting and regulating the JAK/STAT pathway, convenient administration, and rapid onset of action. JAK inhibitors exhibit divergent therapeutic profiles. Clinical trials have shown that tofacitinib demonstrates limited efficacy in Crohn’s disease management. Filgotinib initially showed clinical remission in phase 2 trials; while its subsequent phase 3 studies failed to demonstrate consistent endoscopic improvement. In contrast, upadacitinib achieved notable clinical remission rates during both induction and maintenance phases of phase 2 trials. However, long-term safety concerns, including thromboembolic events, cardiovascular events, opportunistic infections, and potential malignancy risks, warrant cautious clinical application. This article systematically reviews the pathophysiology of Crohn’s disease, and the evidence for the efficacy and safety of JAK inhibitors to guide clinical practice and research.

## Linked entities

- **Chemicals:** tofacitinib (PubChem CID 9926791), filgotinib (PubChem CID 49831257), upadacitinib (PubChem CID 58557659)
- **Diseases:** Crohn’s disease (MONDO:0005011)

## Full-text entities

- **Diseases:** malignancy (MESH:D009369), granulomatous disease (MESH:D006105), inflammatory (MESH:D007249), Crohn's Disease (MESH:D003424), thromboembolic (MESH:D013923), opportunistic infections (MESH:D009894)
- **Chemicals:** Filgotinib (MESH:C584571), tofacitinib (MESH:C479163), upadacitinib (MESH:C000613732)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12189809/full.md

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Source: https://tomesphere.com/paper/PMC12189809