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A thyroxine-containing peptide can induce murine experimental autoimmune thyroiditis

机译:含甲状腺素的肽可诱发鼠实验性自身免疫性甲状腺炎

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摘要

A synthetic peptide based on a sequence containing thyroxine at position 2553 in thyroglobulin (Tg), and already shown to be recognized by two clonotypically distinct murine Tg autoreactive T cell hybridomas, can trigger primed lymph node cells to transfer thyroiditis to naive recipients. Donor lymph node cells could be prepared from mice immunized either with intact mouse Tg or with this peptide itself. After a second exposure to the priming antigen in vitro, both these populations induced 100% thyroiditis in recipient animals. The importance of the T4 residue in the development of disease was demonstrated by the failure of Tg tryptic peptides depleted of T4 to stimulate pathogenic effectors in vitro, even when the lymph node cells had been taken from mice primed with whole Tg. We conclude that this T4- containing 12mer sequence is a major thyroiditogenic epitope in CBA/J mice although we cannot exclude the possibility that there are other pathogenic epitopes present in the whole Tg molecule.
机译:基于在甲状腺球蛋白(Tg)的2553位上含有甲状腺素的序列的合成肽,已被两个克隆型不同的鼠Tg自身反应性T细胞杂交瘤识别,可以触发引发的淋巴结细胞将甲状腺炎转移至幼稚受体。可以从用完整小鼠Tg或该肽本身免疫的小鼠制备供体淋巴结细胞。在第二次在体外暴露于启动抗原后,这两个种群均在受体动物中诱发100%甲状腺炎。耗尽T4的Tg胰蛋白酶肽无法在体外刺激致病效应子,证明了T4残基在疾病发展中的重要性,即使从已用全Tg引发的小鼠中取出淋巴结细胞也是如此。我们得出的结论是,尽管我们不能排除在整个Tg分子中还存在其他致病性抗原表位的可能性,但该包含T4的12mer序列是CBA / J小鼠中主要的促甲状腺激素性抗原表位。

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  • 年度 1992
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  • 正文语种 {"code":"en","name":"English","id":9}
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