Psoriatic arthritis under the influence of IFNγ

Clin Immunol. 2020 Sep:218:108513. doi: 10.1016/j.clim.2020.108513. Epub 2020 Jun 20.

Abstract

Psoriasis is a common multifactorial autoimmune disease of the skin, and in a large percentage of patients, immune responses involve nail and joint pathology, which develop psoriatic arthritis (PsA). Historically, T helper 1 (Th1)-derived-IFN-γ was abundantly detected in psoriatic skin and its correlation with development and severity of PsO, led to an early classification of psoriasis as a Th1-mediated disease. Investigations of the cellular and molecular mechanisms of PsO pathogenesis in recent years, together with impressive results of biologics against interleukin 17A (IL-17) have shifted focus on IL-17A. However, the contributions of IFN-γ in IL-17 induced pathology and its involvement in the development of PsA have been largely overshadowed. This review summarizes the current knowledge on IFN-γ and provides new insights on the contribution of IFN-γ to PsO and PsA disease pathogenesis and development.

Keywords: IFN-γ; IL-17A; Keratinocyte; Osteoclast; Psoriasis; Psoriatic arthritis.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Arthritis, Psoriatic / immunology*
  • Bone Resorption / immunology
  • Humans
  • Immunity, Innate
  • Interferon-gamma / immunology*
  • Interleukin-17 / immunology
  • Synovitis / immunology

Substances

  • Interleukin-17
  • Interferon-gamma