Heterogeneous T cell receptor Vβ gene repertoire in murine interstitial nephritis

• Published in: Kidney international Vol. 49; no. 5; pp. 1222 - 1230
• Main Authors: Heeger, Peter S., Smoyer, William E., Jones, Monica, Hopfer, Suellen, Neilson, Eric G.
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01-05-1996; Nature Publishing
• Subjects: Amino Acid Sequence; Animals; Antigens - administration & dosage; Autoimmune Diseases - etiology; Autoimmune Diseases - genetics; Autoimmune Diseases - immunology; Base Sequence; Basement Membrane - immunology; Biological and medical sciences; Disease Models, Animal; DNA Primers - genetics; Immunization; Interstitial nephritis; Kidney - immunology; Kidney - pathology; Kidney Tubules - immunology; Medical sciences; Mice; Molecular Sequence Data; Nephritis, Interstitial - etiology; Nephritis, Interstitial - genetics; Nephritis, Interstitial - immunology; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Polymerase Chain Reaction; Rabbits; Receptors, Antigen, T-Cell, alpha-beta - genetics; T-Lymphocytes - immunology; Interstitial nephritis; Immunopathology; Urinary system disease; T cell receptor; Variable region; Rodentia; Beta-Peptide chain; Autoimmune disease; Renal disease; Exploration; Heterogeneity; Vertebrata; Mammalia; Gene; Mouse; Animal; T-Lymphocyte; Immunologic repertory
• ISSN: 0085-2538; 1523-1755
• DOI: 10.1038/ki.1996.176

Heterogeneous T cell receptor Vβ gene repertoire in murine interstitial nephritis. Anti-tubular basement membrane disease (αTBM) produces T cell-mediated interstitial nephritis in SJL/J mice following immunization with heterologous renal tubular antigen. Initial mononuclear infiltrates appear in vivo after six to eight weeks, with subsequent progression to renal fibrosis and endstage kidney disease. Cultured lymph node derived nephritogenic T cells from these mice react to a small epitopic region of the 3M-1 target antigen and share a common amino acid motif in their Vβ CDR3 regions. We now have used RT-PCR to further characterize the renal expression of T cell receptor (TcR) Vβ gene repertoires during the course of this disease. Individual kidneys with focal mononuclear infiltrates characteristic of early αTBM disease express up to three different TcR Vβ genes; however, the same Vβ genes are not found in all kidneys at the same early stage of injury. DNA sequencing of the Vβ RT-PCR products reveals a heterogeneous population of VDJ recombinations and deduced CDR3 amino acid sequences. Our studies do not support TcR Vβ region gene restriction in histologically-detectable αTBM disease, but are more consistent with a dynamic, organ-specific autoimmune disease, directed at multiple autoantigenic epitopes.