Diversification of response to hsp65 during the course of autoimmune arthritis is regulatory rather than pathogenic

• Published in: Immunological reviews Vol. 164; no. 1; pp. 175 - 184
• Main Author: Moudgil, Kamal D.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.08.1998
• Subjects: Animals; Arthritis, Experimental - etiology; Arthritis, Experimental - immunology; Bacterial Proteins; Chaperonin 60; Chaperonins - immunology; Epitopes; Models, Immunological; Rats; Rats, Inbred F344; Rats, Inbred Lew
• ISSN: 0105-2896; 1600-065X
• DOI: 10.1111/j.1600-065X.1998.tb01219.x

Determinant spreading has been implicated in the pathogenesis of certain autoimmune diseases in animal models. We have observed that during the course of adjuvant arthritis (AA) in the Lewis rat, there is ‘diversification’ of response to the bacterial 65‐kDa heat shock protein (Bhsp65) towards its carboxy‐terminal determinants (BCTD). Strikingly, pretreatment of naive Lewis rats with BCTD affords significant protection from AA. Our preliminary studies indicate that the diversification of response to BCTD in the Lewis rat is probably triggered in vivo by the induction and enhanced processing of self(rat) hsp65. Thus, the self hsp65‐directed T‐cell responses appear to be involved in mediating natural remission from acute inflammatory arthritis induced by a foreign antigen, Myco‐bacterium tuberculosis. This the first report describing that the new T‐cell specificities arising during the course of an autoimmune disease are regulatory/protective rather than pathogenic. Moreover, our results suggest that a final common mechanism involving BCTD might be recruited by other rac strains which either are resistant to AA (WKY rats) or whose susceptibility to AA is modulated significantly by microbial flora (Fisher rats). The results of this study would contribute significantly to understanding of the pathogenesis of human rheumatoid arthritis, and in devising new therapeutic strategies for this disease.