4.7 Article

IL-33: a Janus cytokine

Journal

ANNALS OF THE RHEUMATIC DISEASES
Volume 71, Issue -, Pages 101-104

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/annrheumdis-2011-200589

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Funding

  1. MRC
  2. Wellcome Trust
  3. European Union
  4. MRC [G0801198, G9818261] Funding Source: UKRI

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Interleukin (IL) 33, a member of the IL-1 family, is the ligand of ST2 that is expressed mainly on activated Th2 cells and mast cells. IL-33 can skew a predominantly Th1 cell population to a mainly Th2 cells phenotype in vivo. IL-33 messenger RNA is expressed early during infection of the intestinal-dwelling nematode Trichuris muris in mice. IL-33 treatment enhances resistance to Trichuris infection. IL-33 also effectively attenuates sepsis by mobilising the innate cells, neutrophils, to the site of infection, helping to clear the pathogens. Thus, IL-33 may be evolutionally preserved for the host defence against infections. IL-33 can reduce an ongoing atherosclerosis in ApoE(-/-) mice and attenuate adipocytes mainly by inducing the production of type II cytokines. In contrast, IL-33 can also exacerbate allergy and the inflammation in collagen-induced or serum-induced arthritis. Hence, IL-33 is a double-edged sword, and targeting IL-33 should be approached with caution.

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