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

被引:131
作者
Andersson, EC
Hansen, BE
Jacobsen, H
Madsen, LS
Andersen, CB
Engberg, J
Rothbard, JB
McDevitt, GS
Malmström, V
Holmdahl, R
Svejgaard, A
Fugger, L [1 ]
机构
[1] Aarhus Univ Hosp, Skejby Sygehus, Dept Clin Immunol, DK-8200 Aarhus N, Denmark
[2] Rigshosp, Dept Clin Immunol, DK-2200 Copenhagen N, Denmark
[3] Rigshosp, Dept Pathol, DK-2200 Copenhagen N, Denmark
[4] Royal Danish Sch Pharm, Dept Biol Sci, DK-2100 Copenhagen O, Denmark
[5] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[6] Lund Univ, Dept Cell & Mol Biol, Sect Med Inflammat Res, S-22100 Lund, Sweden
关键词
D O I
10.1073/pnas.95.13.7574
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 (Cn 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-A(beta)(b)(0) mutation are highly susceptible to collagen-induced arthritis and describe the clinical course and histopathological changes in the affected joints.
引用
收藏
页码:7574 / 7579
页数:6
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