Limited TCR repertoire of infiltrating T cells in the kidneys of Sjögren's syndrome patients with interstitial nephritis

J Immunol. 1995 Oct 15;155(8):4084-9.

Abstract

To analyze the mechanism of interstitial nephritis in patients with Sjörgren's syndrome (SS), we examined the TCR repertoire of infiltration T cells in kidney, labial salivary glands, and PBLs using a PCR. The repertoire of the TCR V beta gene on infiltrating T cells from the kidneys of SS patients was more restricted than those on infiltrating T cells in labial salivary glands and PBL. The TCR V beta 2 gene was expressed predominantly in six of seven (86%) SS patients. Junctional sequences of cDNAs encoding the V beta 2 gene on infiltrating T cells in the kidneys of five SS patients showed that some of the cells expanded clonally, indicating Ag-driven stimulation rather than superantigen-induced proliferation. The same V beta 2 clones in the kidney were not detected in labial salivary glands of the same SS patients; the conserved amino acid (arginine at position 96) in the CDR3 region of the V beta 2 gene was found at a frequency of 48.0% in the kidney, whereas it was detected in only 15.4% of the clones in lips. In conclusion, these findings suggest the possibility that T cells that infiltrate the kidneys of SS patients with interstitial nephritis might recognize different autoantigens than those that infiltrate labial salivary glands.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • CD4-Positive T-Lymphocytes / pathology
  • Cell Movement
  • Humans
  • Kidney / immunology*
  • Kidney / pathology
  • Molecular Sequence Data
  • Nephritis, Interstitial / blood
  • Nephritis, Interstitial / immunology*
  • Nephritis, Interstitial / pathology
  • Receptors, Antigen, T-Cell, alpha-beta / immunology*
  • Salivary Glands, Minor / immunology
  • Salivary Glands, Minor / pathology
  • Sjogren's Syndrome / blood
  • Sjogren's Syndrome / immunology*
  • Sjogren's Syndrome / pathology
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / pathology*

Substances

  • Receptors, Antigen, T-Cell, alpha-beta