首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >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
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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

机译:HLA-DR4限制II型胶原蛋白的免疫优势表位中MHC和T细胞受体接触的定义以及HLA-DR4和人CD4转基因小鼠中胶原蛋白诱发的关节炎的特征

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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 (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-Abβ0 mutation are highly susceptible to collagen-induced arthritis and describe the clinical course and histopathological changes in the affected joints.
机译:类风湿关节炎(RA)是与HLA-DR4和DR1等位基因相关的自身免疫性疾病。 RA中的目标自身抗原未知,但是II型胶原(CII)是候选抗原,并且该蛋白中DR4-和DR1限制性免疫显性T细胞表位对应于氨基酸261-273(CII 261-273) 。我们在CII 261–273中定义了MHC和T细胞受体接触,并提供有力证据表明该肽对应于先前与RA相关的DR分子发现的肽结合特异性。此外,我们证明纯合IA b β 0 突变的HLA-DR4和人CD4转基因小鼠对胶原诱导的关节炎高度敏感,并描述了临床过程和组织病理学受影响关节的变化。

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