AI Article Synopsis

  • Immune-mediated inflammatory diseases (IMIDs) significantly contribute to global health care costs and disease burden, often requiring complex management across different medical specialties.
  • Many patients have overlapping IMIDs, suggesting shared mechanisms and potential for unified treatment approaches, as similar drugs are used across different conditions.
  • A cellular, tissue-based understanding of inflammation could facilitate cross-disease clinical trials, improving drug development efficiency by evaluating treatments for multiple IMIDs simultaneously.

Article Abstract

Immune-mediated inflammatory diseases (IMIDs) are responsible for substantial global disease burden and associated health-care costs. Traditional models of research and service delivery silo their management within organ-based medical disciplines. Very often patients with disease in one organ have comorbid involvement in another, suggesting shared pathogenic pathways. Moreover, different IMIDs are often treated with the same drugs (including glucocorticoids, immunoregulators and biologics). Unlocking the cellular basis of these diseases remains a major challenge, leading us to ask why, if these diseases have so much in common, they are not investigated in a common manner. A tissue-based, cellular understanding of inflammation might pave the way for cross-disease, cross-discipline basket trials (testing one drug across two or more diseases) to reduce the risk of failure of early-phase drug development in IMIDs. This new approach will enable rapid assessment of the efficacy of new therapeutic agents in cross-disease translational research in humans.

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Source
http://dx.doi.org/10.1038/s41584-023-01007-2DOI Listing

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