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ILARIS®—Mechanism of Action

Targeting IL-1β, a Key Driver of Inflammation in Cryopyrin-Associated Periodic Syndromes (CAPS)

CAPS is caused by genetic mutations, often in the NLRP3 (or CIAS1) gene1,2:

  • These mutations result in overproduction of the proinflammatory cytokine, interleukin-1 beta (IL-1β)1
    • Usually autosomal-dominant inherited mutations2

Learn more about the Pathophysiology of CAPS

ILARIS® (canakinumab)—A Monoclonal Antibody That Binds to IL-1β in CAPS1,2

Images of urticaria, conjunctivitis & arthralgia

References:

  • 1. Agostini L, Martinon F, Burns K, McDermott MF, Hawkins PN, Tschopp J. NALP3 forms an IL-1β-processing inflammasome with increased activity in Muckle-Wells autoinflammatory disorder. Immunity. 2004;20:319-325.
  • 2. Hoffman HM, Mueller JL, Broide DH, Wanderer AA, Kolodner RD. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome. Nat Genet. 2001;29:301-305.



isi-Professional www.fda.gov/medwatch full prescribing information