Increased expression of IL-37 in patients with Graves' disease and its contribution to suppression of proinflammatory cytokines production in peripheral blood mononuclear cells

PLoS One. 2014 Sep 16;9(9):e107183. doi: 10.1371/journal.pone.0107183. eCollection 2014.

Abstract

Background: Interleukin-37 (IL-37), a member of IL-1 family, is primarily an anti-inflammatory cytokine, which reduces systemic and local inflammation. However, the expression and role of IL-37 in Graves' disease (GD) remains unknown. This study aims to measure the levels of serum and peripheral blood mononuclear cells (PBMCs) IL-37 in patients with Graves' disease and to examine its association with disease activity. Furthermore, we investigate the effect of IL-37 on proinflammatory cytokines involved in the pathogenesis of GD.

Methods: The expressions of IL-37, TNF-α, IL-6, and IL-17 mRNA in peripheral blood mononuclear cells (PBMCs) of 40 patients with Graves' disease were determined by real-time reverse transcription-polymerase chain reaction (RT-PCR), and the levels of IL-37, TNF-α, IL-6, and IL-17 in serum were detected by enzyme-linked immunoassay (ELISA). The correlation of serum IL-37 levels with cytokines and disease activity in Graves' disease patients were investigated. The expressions of cytokines TNF-α, IL-6, and IL-17 in PBMCs under recombinant IL-37 stimulation were determined by RT-PCR and ELISA respectively.

Results: The levels of IL-37, TNF-α, IL-6, and IL-17 in PBMCs and serum were significantly increased in patients with GD compared with healthy controls (HC). Serum IL-37 were closely correlated with TNF-α, IL-6, IL-17, thyrotropin (TSH), free thyroxine (FT4),free triiodothyronine (FT3) and thyrotropin receptor antibody (TRAB). GD patients with active disease showed higher IL-37 mRNA and serum protein levels compared with those with inactive disease as well as HC. Moreover, IL-37 suppressed the production of IL-6, IL-17 and TNF-α in PBMCs of patients with GD.

Conclusions: Increased level of IL-37 in patients with GD are associated with TNF-α, IL-6, IL-17 and disease activity, and it plays a protective role against inflammatory effect in GD by inhibiting the production of proinflammatory cytokines. Thus, IL-37 may provide a novel research target for the pathogenesis and therapy of GD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Case-Control Studies
  • Cytokines / blood
  • Cytokines / genetics
  • Cytokines / metabolism*
  • Female
  • Gene Expression Regulation
  • Gene Expression*
  • Graves Disease / diagnosis
  • Graves Disease / genetics*
  • Graves Disease / metabolism*
  • Humans
  • Inflammation Mediators / metabolism*
  • Interleukin-1 / blood
  • Interleukin-1 / genetics*
  • Interleukin-1 / metabolism
  • Leukocytes, Mononuclear / metabolism*
  • Male
  • Middle Aged
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Young Adult

Substances

  • Cytokines
  • IL37 protein, human
  • Inflammation Mediators
  • Interleukin-1
  • RNA, Messenger

Grants and funding

This work was supported by grants from the National Natural Science Foundation of China (No: 81273305), the Basic Research Program of Science and Technology Plan of Shenzhen (No: JC201005280578A), and the Special Program of Construction National Innovative City of Shenzhen (No: 301201003010). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.