4.7 Article

Dichotomous function of IL-33 in health and disease: From biology to clinical implications

Journal

BIOCHEMICAL PHARMACOLOGY
Volume 148, Issue -, Pages 238-252

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bcp.2018.01.010

Keywords

IL-33; Allergy; Asthma; Inflammation; Signaling; Immunity

Funding

  1. Fund for Scientific Research Flanders (FWO) [G035517N, G090914N]
  2. Foundation Against Cancer [FAF-F/2016/812]
  3. Ghent University Concerted Research Actions (GOA) [BOF13-GOA-005]
  4. Ghent University Industrial Research Fund (IOF)
  5. FWO [1503815N, 1503418N]

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Interleukin (IL)-33 is a cytokine that is released from epithelial and endothelial cells at barrier surfaces upon tissue stress or damage to operate as an alarmin. IL-33 has been primarily implicated in the induction of T helper (Th) 2 type immune responses. Therefore, IL-33 has attracted a lot of interest as a potential therapeutic target in asthma and other allergic diseases. Over the years, it has become clear that IL-33 has a much broader activity and also contributes to Th1 immunity, expanding the possibilities for therapeutic modulation of IL-33 activity to multiple inflammatory diseases. However, more recently IL-33 has also been shown to mediate immunosuppression and tissue repair by activating regulatory T cells (Treg) and promoting M2 macrophage polarization. These pleiotropic activities of IL-33 illustrate the need for a tight molecular regulation of IL-33 activity, and have to be taken into account when IL-33 or its receptor is targeted for therapeutic modulation. Here we review the multiple molecular mechanisms that regulate IL-33 activity and describe how I -33 can shape innate and adaptive immune responses by promoting Th1, Th2 and Treg function. Finally, we will discuss the possibilities for therapeutic modulation of IL-33 signaling as well as possible safety issues. (C) 2018 Elsevier Inc. All rights reserved.

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