Jones D B, Coulson A F, Duff G W
Dept of Medicine, Arrowe Park Hospital, Liverpool, Merseyside, UK.
Immunol Today. 1993 Mar;14(3):115-8. doi: 10.1016/0167-5699(93)90210-C.
The human heat shock protein (hsp) 60 shares sequence homology with a wide range of autoantigens including those of insulin dependent diabetes mellitus, Hashimoto's thyroiditis, glomerulonephritis, scleroderma, pemphigoid, rheumatoid arthritis, multiple sclerosis, chronic active hepatitis, primary biliary cirrhosis and Addison's disease. Here we show the extent of this homology and suggest that it contributes to autoimmunity through cross-reactivity between hsp60 and tissue-specific proteins containing similar epitope motifs. Differences between individuals in MHC class II may influence the selection of a particular hsp60 epitope and the corresponding target antigen that gives rise to an autoimmune disease.
人类热休克蛋白(hsp)60与多种自身抗原具有序列同源性,这些自身抗原包括胰岛素依赖型糖尿病、桥本甲状腺炎、肾小球肾炎、硬皮病、类天疱疮、类风湿性关节炎、多发性硬化症、慢性活动性肝炎、原发性胆汁性肝硬化和艾迪生病的自身抗原。在此我们展示了这种同源性的程度,并提出它通过hsp60与含有相似表位基序的组织特异性蛋白之间的交叉反应促成自身免疫。个体之间MHC II类分子的差异可能影响特定hsp60表位以及引发自身免疫疾病的相应靶抗原的选择。