Ben-Nun A, Maron R, Ron Y, Cohen I R
Eur J Immunol. 1980 Feb;10(2):156-9. doi: 10.1002/eji.1830100216.
The restriction of the pathogenesis of experimental autoimmune thyroiditis (EAT) by H-2 gene products was investigated. EAT was induced by injecting thyroglobulin extract plus adjuvant into F1 hybrid mice that had been implanted under the kidney capsules with thyroid glands originating from either the EAT-susceptible or -resistant parental strain mice. We found relative H-2 restriction of thyroid damage to those glands originating from the H-2 susceptible parental strain. H-2 restriction of damage at the level of the target thyroid gland implicates cytotoxic effector T lymphocytes as a pathogenic agent of EAT.
研究了H-2基因产物对实验性自身免疫性甲状腺炎(EAT)发病机制的限制作用。通过将甲状腺球蛋白提取物加佐剂注射到已在肾包膜下植入来自EAT易感或抗性亲代品系小鼠甲状腺的F1杂交小鼠中诱导EAT。我们发现甲状腺损伤对源自H-2易感亲代品系的甲状腺存在相对的H-2限制。靶甲状腺水平的损伤的H-2限制表明细胞毒性效应T淋巴细胞是EAT的致病因子。