[Interleukin-1, inflammasome and autoinflammatory diseases]

Rev Med Interne. 2018 Apr;39(4):233-239. doi: 10.1016/j.revmed.2016.07.007. Epub 2016 Sep 14.
[Article in French]

Abstract

Interleukin-1 is a major cytokine of innate immunity and inflammation. It exerts various systemic effects during the inflammatory response, such as fever induction, thrombopoiesis and granulopoiesis, or leukocyte recruitment. Its involvement has been demonstrated in many inflammatory-mediated diseases, such as diabetes or gout. Moreover, interleukin-1 plays a pivotal role in some autoinflammatory diseases, such as cryopyrinopathies or familial Mediterranean fever. In these diseases, a constitutional defect of the inflammasome, a protein complex responsible for the activation of interleukin-1, explains the hypersecretion of interleukin-1. Other autoinflammatory diseases have a more complex pathophysiology involving deregulation of the interleukin-1 pathway, upstream or downstream of the inflammasome, or through more complex mechanisms. In this review, we are detailing the synthesis, the activation, the signalling, and the regulation of interleukin-1. We then describe the autoinflammatory diseases or related-diseases where the pathological role of interleukin-1 has been demonstrated.

Keywords: Anakinra; Auto-inflammation; Maladie de Still; NLRP3; Pyrin; Pyrine; Still's disease.

Publication types

  • Review

MeSH terms

  • Genetic Predisposition to Disease
  • Hereditary Autoinflammatory Diseases / genetics
  • Hereditary Autoinflammatory Diseases / metabolism*
  • Humans
  • Inflammasomes / metabolism*
  • Interleukin-1 / metabolism*
  • Mutation

Substances

  • Inflammasomes
  • Interleukin-1