1. Academic Validation
  2. Interleukin-23: as a drug target for autoimmune inflammatory diseases

Interleukin-23: as a drug target for autoimmune inflammatory diseases

  • Immunology. 2012 Feb;135(2):112-24. doi: 10.1111/j.1365-2567.2011.03522.x.
Chunlei Tang 1 Shu Chen Hai Qian Wenlong Huang
Affiliations

Affiliation

  • 1 Centre of Drug Discovery, State Key Laboratory of Bioactive Natural Products and Function, China.
Abstract

Interleukin-23 (IL-23) is a member of the IL-12 family of cytokines with pro-inflammatory properties. Its ability to potently enhance the expansion of T helper type 17 (Th17) cells indicates the responsibility for many of the inflammatory autoimmune responses. Emerging data demonstrate that IL-23 is a key participant in central regulation of the cellular mechanisms involved in inflammation. Both IL-23 and IL-17 form a new axis through Th17 cells, which has evolved in response to human diseases associated with immunoactivation and immunopathogeny, including Bacterial or viral infections and chronic inflammation. Targeting of IL-23 or the IL-23 Receptor or IL-23 axis is a potential therapeutic approach for autoimmune diseases including psoriasis, inflammatory bowel disease, rheumatoid arthritis and multiple sclerosis. The current review focuses on the immunobiology of IL-23 and summarizes the most recent findings on the role of IL-23 in the pre-clinical and ongoing clinical studies.

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