Role of interleukin-32 in the mechanism of chronic inflammation in IgG4-related disease and as a predictive biomarker for drug-free remission

Mod Rheumatol. 2016;26(3):391-7. doi: 10.3109/14397595.2015.1089973. Epub 2015 Oct 19.

Abstract

Objectives: In immunoglobulin (Ig) G4-related disease (IgG4-RD), the mechanism of chronic inflammation and predictive factors for drug-free remission is still unclear. To examine the issues, we focused on tuberculosis, a chronic infection, and on the role of interleukin (IL)-32.

Methods: We examined the positive rate of QuantiFERON TB-2G (QFT-2G) in 126 patients with IgG4-RD, and compared with the rate in the general population. Furthermore, specimens of submandibular glands from the maintenance treatment group and drug-free group of IgG4-RD and specimens of small salivary glands from primary Sjögren's syndrome (SS) were stained with anti-IL-32 antibody and anti-protease-activated receptor 2 antibody, and the number of positive cells was compared between these groups.

Results: The positive rate of QFT-2G was 19.8% in IgG4-RD patients, which is higher than in the general population. The expression of IL-32 and PAR2 in the submandibular glands of the maintenance treatment group of IgG4-RD was significantly greater than that of the drug-free remission group and SS patients.

Conclusions: This study indicates the possibility that IL-32 is associated with chronic inflammation and that it can be a predictive factor for drug-free remission in IgG4-RD.

Keywords: Chronic inflammation; Germinal center; IgG4-related disease; Interleukin-32; Tuberculosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers / metabolism
  • Female
  • Humans
  • Immunoglobulin G / immunology*
  • Inflammation / immunology
  • Inflammation / metabolism
  • Interleukins / metabolism*
  • Male
  • Middle Aged
  • Receptor, PAR-2 / metabolism
  • Salivary Glands / immunology
  • Salivary Glands / metabolism*
  • Sjogren's Syndrome / immunology
  • Sjogren's Syndrome / metabolism*
  • Tuberculosis / immunology
  • Tuberculosis / metabolism*

Substances

  • Biomarkers
  • IL32 protein, human
  • Immunoglobulin G
  • Interleukins
  • Receptor, PAR-2