Kohn L D, Alvarez F, Marcocci C, Kohn A D, Corda D, Hoffman W E, Tombaccini D, Valente W A, de Luca M, Santisteban P
Ann N Y Acad Sci. 1986;475:157-73. doi: 10.1111/j.1749-6632.1986.tb20865.x.
The present report summarizes experiments with monoclonal antibodies to the TSH receptor. The data provide further insight into the TSH receptor structure and into the basis of autoimmune antibodies implicated in the pathogenesis of Graves' disease. They resolve many clinical questions and provide new approaches to enhance our understanding of autoimmune disease. In one new approach, it has been noted that the 11E8 TBIAb can precipitate the phosphorylated beta subunit of the insulin and IGF1 receptor. This cross-reactivity or recognition of determinants adjacent to the TSH receptor may not be random. Insulin, IGF1, alpha 1 adrenergic, and TSH receptors have been linked to a synergistic cascade response system of the thyroid involving growth, thyroglobulin biosynthesis, iodination of thyroglobulin, and thyroid hormone formation. Future studies with the monoclonals may help unravel this cascade system and its regulatory relationships, along with the relationships between autoimmune thyroid disease and autoimmune diseases of other organs.
本报告总结了针对促甲状腺激素(TSH)受体的单克隆抗体实验。这些数据进一步深入了解了TSH受体结构以及与格雷夫斯病发病机制相关的自身免疫抗体的基础。它们解决了许多临床问题,并提供了新方法以增进我们对自身免疫性疾病的理解。在一种新方法中,已注意到11E8 TBIAb可沉淀胰岛素和胰岛素样生长因子1(IGF1)受体的磷酸化β亚基。这种与TSH受体相邻的决定簇的交叉反应性或识别可能并非随机。胰岛素、IGF1、α1肾上腺素能受体和TSH受体已与甲状腺的协同级联反应系统相关联,该系统涉及生长、甲状腺球蛋白生物合成、甲状腺球蛋白碘化以及甲状腺激素形成。未来使用单克隆抗体的研究可能有助于阐明此级联系统及其调节关系,以及自身免疫性甲状腺疾病与其他器官自身免疫性疾病之间的关系。