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DRB1链第74位疏水氨基酸在类风湿性关节炎中的作用。

Role of hydrophobic amino acids at position 74 of DRB1 chain in rheumatoid arthritis.

作者信息

Cerná M, Havelka S, Ivasková E

机构信息

Department of Immunology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.

出版信息

Arch Immunol Ther Exp (Warsz). 1995;43(2):139-44.

PMID:8744729
Abstract

We have analyzed HLA class II alleles in a group of 153 Czech children with rheumatoid arthritis by PCR and hybridization with oligonucleotide probes. When we try to find a common sequence for all DRB1 alleles involved in juvenile and adult arthritis, we can notice hydrophobic amino acid at position 74, which is present in all these alleles, but not in nonsusceptible alleles, where is the hydrophilic amino acid at position 74. In our model, we speculate that the hydrophilic amino acid at position 74 creates a such kind of epitope which is not suitable for rheumatoid-associated peptides or T cells, and only hydrophobic amino acid can permit binding of these peptides or recognition by certain T cells. Analyses of the DPB1 sequences have shown that alleles which have a negatively charged amino acid at position 69, are more frequent in pauciarticular patients while those with a positively charged amino acid are more frequent in polyarticular patients. A positively charged amino acid at position 69 might present the same rheumatoid associated peptide as susceptible DRB1 alleles. The presence of more rheumatoid-associated peptide on the cell surface may cause conversion to more severe polyarticular forms. A negatively charged amino acid at position 69 could not present this peptide and a low concentration of the peptide on the cell surface presented just by DRB1 molecules keeps disease in a relatively benign condition of pauciarticular forms.

摘要

我们通过聚合酶链反应(PCR)以及与寡核苷酸探针杂交,分析了153名患类风湿性关节炎的捷克儿童的HLA - II类等位基因。当我们试图找出参与青少年和成人关节炎的所有DRB1等位基因的共同序列时,我们注意到在第74位存在疏水氨基酸,所有这些等位基因中都有该氨基酸,而在非易感等位基因中,第74位是亲水氨基酸。在我们的模型中,我们推测第74位的亲水氨基酸形成了一种不适用于类风湿相关肽或T细胞的表位,只有疏水氨基酸才能允许这些肽结合或被某些T细胞识别。对DPB1序列的分析表明,在第69位有带负电荷氨基酸的等位基因在少关节型患者中更常见,而带正电荷氨基酸的等位基因在多关节型患者中更常见。第69位带正电荷的氨基酸可能与易感DRB1等位基因呈现相同的类风湿相关肽。细胞表面存在更多类风湿相关肽可能导致转变为更严重的多关节型。第69位带负电荷的氨基酸不能呈现这种肽,仅由DRB1分子在细胞表面呈现的低浓度肽使疾病处于少关节型的相对良性状态。

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