Pediatric Rheumatology Online Journal (Jan 2024)

The 4th NextGen therapies of SJIA and MAS, part 4: it is time for IL-18 based trials in systemic juvenile idiopathic arthritis?

  • Scott W. Canna,
  • Fabrizio De Benedetti

DOI
https://doi.org/10.1186/s12969-023-00867-y
Journal volume & issue
Vol. 21, no. S1
pp. 1 – 6

Abstract

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Abstract Since IL-18 has recently emerged as a biomarker associated with refractory disease course in SJIA, the focus of the discussion was the feasibility of the biomarker-driven drug development to SJIA. Overall, there was broad agreement on the conclusion that IL-18 is a uniquely specific biomarker for many of the subsets of SJIA most in need of new therapies, and it may define a class of diseases mediated by IL-18 excess. The consensus was that leveraging IL-18 remains our most promising “lead” for use in refractory SJIA as it may mechanistically explain the disease pathophysiology and lead to more targeted therapies.

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