Expanded double negative T cells in patients with systemic lupus erythematosus produce IL-17 and infiltrate the kidneys

J Immunol. 2008 Dec 15;181(12):8761-6. doi: 10.4049/jimmunol.181.12.8761.

Abstract

Double negative (DN) T cells are expanded in patients with systemic lupus erythematosus (SLE) and stimulate autoantibody production as efficiently as CD4(+) T cells. In this study, we demonstrate that DN T cells from patients with SLE produce significant amounts of IL-17 and IFN-gamma, and expand when stimulated in vitro with an anti-CD3 Ab in the presence of accessory cells. Furthermore, IL-17(+) and DN T cells are found in kidney biopsies of patients with lupus nephritis. Our findings establish that DN T cells produce the inflammatory cytokines IL-17 and IFN-gamma, and suggest that they contribute to the pathogenesis of kidney damage in patients with SLE.

Publication types

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

MeSH terms

  • Adult
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / pathology
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / pathology
  • Cell Movement / immunology*
  • Cell Proliferation*
  • Cells, Cultured
  • Humans
  • Immunophenotyping
  • Inflammation Mediators / metabolism
  • Inflammation Mediators / physiology
  • Interleukin-17 / biosynthesis*
  • Kidney / immunology*
  • Kidney / pathology
  • Lupus Erythematosus, Systemic / immunology*
  • Lupus Erythematosus, Systemic / metabolism
  • Lupus Erythematosus, Systemic / pathology
  • Middle Aged
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocyte Subsets / pathology
  • Up-Regulation / immunology

Substances

  • Inflammation Mediators
  • Interleukin-17