IL-23/Th17 Axis: A Potential Therapeutic Target of Psoriasis

Curr Drug Res Rev. 2022;14(1):24-36. doi: 10.2174/2589977513666210707114520.

Abstract

Psoriasis is an immune-mediated skin disease that leads to the initiation of abnormal production of inflammatory mediators and keratinocytes hyper-proliferation. Th-1 cell expressing cytokines such as IL-1β and TNF-α have been the important hallmarks in the management of psoriasis. However, investigations carried out in the previous few years underline the involvement of another subset of T helper cells, i.e. Th-17 in psoriasis exacerbation, and hence have become the point of focus now. The immunopathogenesis of Th-17 is the result of the IL-23/Th-17 axis. It involves the release of IL-17 and IL-22 in response to the activated NF-kβ dependent activation of IL-23. The function of human Th-17 cells, as well as the crucial role of IL-23/Th-17 axis in the exacerbation of psoriasis and treatment, have been well explored. Therefore, considering IL-23/Th17 axis as a pertinent therapeutic target in immune driven disorders, extensive investigations are now highlighting the utility of biopharmaceuticals and/or biological agents acting on these targets. Here, we review the IL-23/Th-17 axis based therapeutic targets, different types of active moieties based on their source of availability and most useful USFDA approved Mabs targeting the IL-23/Th17 axis in psoriasis for a better understanding of the future possibilities in this area.

Keywords: IL-23/Th-17 axis; Psoriasis; Th-17 cells; biological agents; biopharmaceuticals; therapeutic targets.

Publication types

  • Review

MeSH terms

  • Cytokines / metabolism
  • Cytokines / therapeutic use
  • Humans
  • Interleukin-23 / metabolism
  • Psoriasis* / drug therapy
  • Th17 Cells* / metabolism
  • Th17 Cells* / pathology
  • Tumor Necrosis Factor-alpha / metabolism
  • Tumor Necrosis Factor-alpha / therapeutic use

Substances

  • Cytokines
  • Interleukin-23
  • Tumor Necrosis Factor-alpha