DPP4 reduces proinflammatory cytokine production in human rheumatoid arthritis synovial fibroblasts

J Cell Physiol. 2021 Dec;236(12):8060-8069. doi: 10.1002/jcp.30494. Epub 2021 Jun 30.

Abstract

Rheumatoid arthritis (RA) is an autoimmune disorder that is characterized by increasing levels of proinflammatory cytokines. The ubiquitous enzyme dipeptidyl peptidase-4 (DPP4, also known as CD26) regulates different immune disorders, although the effects of DPP4 in RA are uncertain. Here, we found lower levels of DPP4 in RA synovial tissues compared with normal tissues. DPP4 levels were also lower in a rat collagen-induced arthritis model than in control (healthy) rats. Overexpression of DPP4 or exogenous treatment of RA synovial fibroblasts with DPP4 reduced levels of proinflammatory interleukin (IL)-1β, IL-6, and IL-13, and increased anti-inflammatory IL-10 synthesis, while DPP4 inhibitors sitagliptin and vildagliptin increased proinflammatory cytokine production, indicating an enhanced risk of RA development. The evidence suggests that increasing DPP4 expression is a novel strategy for RA disease.

Keywords: DPP4; cytokine; rheumatoid arthritis; sitagliptin; vildagliptin.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Arthritis, Rheumatoid / drug therapy*
  • Arthritis, Rheumatoid / metabolism
  • Cytokines / drug effects*
  • Cytokines / metabolism
  • Dipeptidyl Peptidase 4* / metabolism
  • Dipeptidyl Peptidase 4* / pharmacology
  • Fibroblasts / drug effects*
  • Fibroblasts / metabolism
  • Humans
  • Inflammation / drug therapy
  • Inflammation / metabolism
  • Synovial Membrane / drug effects
  • Synovial Membrane / metabolism

Substances

  • Cytokines
  • Dipeptidyl Peptidase 4