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January 14, 2026Biomedicines0 citationsOpen Access

Treatment of Inflammatory Bowel Disease with Drugs Targeting PANoptosis: A Comprehensive Review

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JTJohn K. TriantafillidisSKStavros Karakatsanis

Key Points

  • Evaluate the role of PANoptosis in inflammatory bowel disease and its therapeutic potential.
  • Reviewed recent literature and clinical trial data regarding programmed cell death inhibitors and natural compounds in IBD models.
  • Targeting PANoptotic regulators like RIPK1 and ZBP1 can restore barrier integrity.
  • IL-1/IL-18 inhibitors like Anakinra showed promise but have disappointing clinical results.
  • RIPK1 inhibitors such as GSK2982772 failed to meet primary endpoints in Phase 2 trials.

Abstract

Background: Inflammatory Bowel Disease (IBD) involves a complex interplay between immune dysregulation and intestinal barrier failure. Traditional views focused on individual cell death pathways, but the emerging concept of PANoptosis—a coordinated inflammatory cell death involving apoptosis, necroptosis, and pyroptosis—offers a more holistic understanding of IBD pathogenesis. Objective: This review evaluates the role of PANoptosis in IBD, identifies key molecular triggers (such as the ZBP1-ADAR1 axis), and discusses the therapeutic potential of targeting this process. Methods: We analyzed recent literature and clinical trial data regarding programmed cell death (PCD) inhibitors and natural compounds in IBD models. Results: Preclinical data suggest that targeting PANoptotic regulators like RIPK1 and ZBP1 can restore barrier integrity. However, clinical translation remains challenging; for instance, while targeting pyroptosis via IL-1/IL-18 (Anakinra) showed promise in theory, clinical results in IBD have been disappointing. Furthermore, RIPK1 inhibitors such as GSK2982772 have failed to meet primary endpoints in Phase 2 trials. Conclusions: PANoptosis is a “hot” therapeutic target, but successful treatment likely requires combination therapies or “PANoptosome” specific modulators rather than single-pathway inhibition.

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Triantafillidis et al. (2026) studied this question.

synapsesocial.com/papers/6966f33b13bf7a6f02c011fdhttps://doi.org/10.3390/biomedicines14010148
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