Expression of a type II collagen-specific TCR transgene accelerates the onset of arthritis in mice

Int Immunol. 1998 Nov;10(11):1613-22. doi: 10.1093/intimm/10.11.1613.

Abstract

Animal models of autoimmune diseases have been instrumental in advancing our understanding of autoimmunity in humans. Collagen-induced arthritis in mice is an autoimmune disease model of rheumatoid arthritis, which is MHC class II restricted and CD4 T cell dependent. To better understand the fundamental role of T cells in arthritis, we have generated a transgenic mouse carrying the rearranged Valpha11.1 and Vbeta8.2 TCR chain genes isolated from a type II collagen (CII)-specific T cell hybridoma. Cell surface analysis indicated that Vbeta8.2 chain was expressed on the surface of nearly all peripheral T cells. Analysis of T cell subsets in transgenic mice revealed a profound skewing in peripheral T cells towards the CD4 population. Although peripheral T cells were not tolerant to CII and responded to CII stimulation in vitro, transgenic mice did not develop spontaneous arthritis. However, a rapid onset of arthritis with severe clinical signs was detected in transgenic mice after immunization with CII in complete Freund's adjuvant. Histological analysis of inflamed joints showed a great resemblance to arthritic joints in man. This unique transgenic mouse model provides valuable insights into the mechanism of arthritis and into potential specific immune interventions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arthritis, Rheumatoid / immunology*
  • Arthritis, Rheumatoid / pathology
  • B-Lymphocytes
  • CD4-Positive T-Lymphocytes / immunology*
  • Collagen / immunology*
  • Disease Models, Animal
  • Flow Cytometry
  • Gene Rearrangement, alpha-Chain T-Cell Antigen Receptor
  • Gene Rearrangement, beta-Chain T-Cell Antigen Receptor
  • Hybridomas
  • Immune Tolerance
  • Joints / pathology
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred DBA
  • Mice, Transgenic
  • Receptors, Antigen, T-Cell, alpha-beta / genetics*
  • Receptors, Antigen, T-Cell, alpha-beta / immunology*
  • Spleen / cytology
  • Spleen / immunology
  • Thymus Gland / cytology
  • Thymus Gland / immunology
  • Transgenes*

Substances

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