Roles of IL-17, Th1, and Tc1 cells in patients with IgG4-related sclerosing sialadenitis

Laryngoscope. 2012 Oct;122(10):2169-74. doi: 10.1002/lary.23429. Epub 2012 Jul 11.

Abstract

Objectives/hypothesis: Immunoglobulin G4 (IgG4)-related sclerosing sialadenitis is a recently recognized disease entity characterized by high serum IgG4 concentration and IgG4-producing plasma cell expansion in affected organs, which show fibrotic or sclerotic changes. However, little is known about the roles of CD4+ and CD8+ T cells or interleukin (IL)-17 in this disease. The purpose of this study was to evaluate the characteristics of CD4+ and CD8+ T cells and IL-17 in patients with IgG4-related sclerosing sialadenitis.

Study design: A retrospective clinical study at the Yamagata University School of Medicine.

Methods: The patient group consisted of six males and four females with an average age of 57.9 years (range, 38 to 73 years). Subsets of T helper (Th)1, Th2, T cytotoxic type (Tc)1, and Tc2 cells from patients with IgG4-related sclerosing sialadenitis were examined by using intracellular cytokine flow cytometry. Expression of IL-17 in the patients' lesions was also investigated immunohistochemically.

Results: Six patients with IgG4-related sclerosing sialadenitis with high ratios of IgG4/IgG and prominent infiltration of IgG4-positive plasmacytes in the involved salivary glands had systemic complications, including pancreatitis, retroperitoneal fibrosis, and/or inflammatory pseudotumor of the lung after the initial swelling of the salivary glands. Populations of Th1 and Tc1 cells were significantly greater in IgG4-related sclerosing sialadenitis than in the controls (P < .05), but Th2 and Tc2 cell populations were not significantly increased. Expression of IL-17 was observed in the lesions of affected patients.

Conclusions: Increases in Th1 and Tc1 cell populations and IL-17 expression might be involved in the mechanism of pathogenesis of IgG4-related sclerosing sialadenitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Female
  • Flow Cytometry
  • Humans
  • Immunoglobulin G / blood*
  • Immunohistochemistry
  • Interleukin-17 / blood*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Sclerosis
  • Sialadenitis / blood*
  • Sialadenitis / pathology*
  • T-Lymphocytes, Cytotoxic / pathology
  • Th1 Cells / pathology*

Substances

  • Immunoglobulin G
  • Interleukin-17