Background: Interleukin (IL)-23, a member of the IL-12 family, has emerged as an important cytokine that bridges the innate and adaptive immune systems and plays a critical role in the development of a wide spectrum of immune-mediated inflammatory disorders (IMIDs). It can be considered a gatekeeper of T helper 17 (Th17) cells development and expansion that subsequently produces several mediators that promote inflammation. The inhibition of IL-23 is a potential therapeutic approach for several inflammatory diseases, such as psoriasis, psoriatic arthritis, and inflammatory bowel disease.
Objective: This work aims to address the overview of the immunobiology of IL-23 associated with some of the most frequent IMIDs and the current pipeline of its inhibition.
Methods: We conducted a narrative review elucidating data about 1) the overview of the immunobiology of IL-23 associated with immune-mediated inflammatory disorders in specific diseases, such as psoriasis, psoriatic arthritis, and inflammatory bowel disease; 2) therapeutic approaches targeting the IL-23 pathway (IL-23 inhibitor drugs approved by international agencies); and 3) novel therapeutic perspectives. The search strategy was conducted in the relevant database with terms related to the proximity to IL-23 or immuno-mediated.
Results and conclusions: Existing and emerging therapeutic biologics targeting the IL-23/IL-17 pathway are promising options to treat IMIDs while the knowledge of the pathophysiology of those conditions and the contribution of the IL23/IL-17 continues to grow. J Drugs Dermatol. 2023;22(4): doi:10.36849/JDD.7017 Citation: Galli Sanchez AP, Castanheiro da Costa A, Del Rey C, et al. The overview of the immunobiology of interleukin-23 associated with immune-mediated inflammatory disorders. A narrative review. J Drugs Dermatol. 2023;22(4):375-385. doi:10.36849/JDD.7017.