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与HLA-DR蛋白结合并抑制II型胶原反应性T细胞克隆的合成氨基酸共聚物。

Synthetic amino acid copolymers that bind to HLA-DR proteins and inhibit type II collagen-reactive T cell clones.

作者信息

Fridkis-Hareli M, Rosloniec E F, Fugger L, Strominger J L

机构信息

Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Oct 13;95(21):12528-31. doi: 10.1073/pnas.95.21.12528.

Abstract

Copolymer 1 [poly(Y,E,A,K)] is a random synthetic amino acid copolymer of L-tyrosine, L-glutamic acid, L-alanine, and L-lysine that is effective both in suppression of experimental allergic encephalomyelitis and in the treatment of relapsing forms of multiple sclerosis. Copolymer 1 binds promiscuously and very efficiently to purified HLA-DR molecules within the peptide-binding groove. In the present study, YEAK and YEAK-related copolymers and type II collagen (CII) peptide 261-273, a candidate autoantigen in rheumatoid arthritis (RA), competed for binding to RA-associated HLA-DR molecules encoded by DRB10101 and DRB10401. Moreover, these copolymers (particularly YEAK, YAK, and YEK) inhibited the response of DR1- and DR4-restricted T cell clones to the CII epitope 261-273 by >50%. This direct evidence both for competitive interactions of these copolymers and CII peptide with RA-associated HLA-DR molecules and for inhibition of CII-specific T cell responses suggests that these compounds should be evaluated in animal models for rheumatoid arthritis.

摘要

共聚体1 [聚(Y、E、A、K)]是一种由L-酪氨酸、L-谷氨酸、L-丙氨酸和L-赖氨酸组成的随机合成氨基酸共聚体,它在抑制实验性变应性脑脊髓炎以及治疗复发型多发性硬化症方面均有效。共聚体1能杂乱且非常有效地与肽结合槽内的纯化HLA-DR分子结合。在本研究中,YEAK及与YEAK相关的共聚体以及II型胶原(CII)肽261 - 273(类风湿关节炎(RA)中的一种候选自身抗原)竞争结合由DRB10101和DRB10401编码的RA相关HLA-DR分子。此外,这些共聚体(尤其是YEAK、YAK和YEK)抑制DR1和DR4限制性T细胞克隆对CII表位261 - 273的反应达50%以上。这些共聚体与CII肽和RA相关HLA-DR分子之间竞争性相互作用以及对CII特异性T细胞反应的抑制的这一直接证据表明,这些化合物应在类风湿关节炎动物模型中进行评估。

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