Definition of MHC and T cell receptor contacts in the HLA-DR4restricted immunodominant epitope in type II collagen and characterization of collagen-induced arthritis in HLA-DR4 and human CD4 transgenic mice

Ellen Andersson(Aarhus University Hospital), Bjarke Endel Hansen(Aarhus University Hospital), Helle J. Jacobsen(Aarhus University Hospital), Lars Siim Madsen(Aarhus University Hospital), Claus B. Andersen(Aarhus University Hospital), Jan Engberg(Aarhus University Hospital), Jonathan B. Rothbard(Aarhus University Hospital), Grete Sønderstrup McDevitt(Aarhus University Hospital), Vivianne Malmström(Aarhus University Hospital), Rikard Holmdahl(Aarhus University Hospital), Arne Svejgaard(Aarhus University Hospital), Lars Fugger(Aarhus University Hospital)
Proceedings of the National Academy of Sciences
June 23, 1998
Cited by 149Open Access

Abstract

Rheumatoid arthritis (RA) is an autoimmune disease associated with the HLA-DR4 and DR1 alleles. The target autoantigen(s) in RA is unknown, but type II collagen (CII) is a candidate, and the DR4- and DR1-restricted immunodominant T cell epitope in this protein corresponds to amino acids 261-273 (CII 261-273). We have defined MHC and T cell receptor contacts in CII 261-273 and provide strong evidence that this peptide corresponds to the peptide binding specificity previously found for RA-associated DR molecules. Moreover, we demonstrate that HLA-DR4 and human CD4 transgenic mice homozygous for the I-Abbeta0 mutation are highly susceptible to collagen-induced arthritis and describe the clinical course and histopathological changes in the affected joints.


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