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Immunization with thyroglobulin induces Graves-like disease in mice

机译:甲状腺球蛋白免疫可诱发小鼠Graves样疾病

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摘要

We immunized AKR/N mice with bovine thyroglobulin (Tg) once every 2 weeks and monitored their time-dependent changes in 125I uptake activity in the thyroid glands. After 3 months, anti-Tg antibody was positive in all sera from the immunized mice. Serum free tri-iodothyronine (T3) and free thyroxine (T4) levels in the immunized mice (n=6) were significantly higher than those in the saline injected (control) mice (n=6). Neck counts as well as scintigraphy of the thyroid glands revealed that iodide uptake activity of the immunized mice was not suppressed, but was instead higher than that of the control mice. Two of the six immunized mice showed extremely high iodide uptake activity. The thyroid glands of these two mice were diffusely enlarged and the height of the epithelial cells was also increased. In addition, two mice with high iodide uptake activity produced a high titer of thyroid-stimulating antibody. Additional experiments showed that 4 out of 11 AKR/N mice and 3 out of 10 C57BL6 mice immunized with Tg had high serum free T3/free T4 levels, high 125I uptake activity of the thyroid, and positive thyroid-stimulating antibody activity. Diffuse goiter, thyrotoxicosis, high iodide uptake activity, and positive thyroid-stimulating antibody are the characteristics of Graves' disease. Thus, these mice exhibit the symptoms of Graves' disease. These results suggest that immunization with Tg induces Graves'-like disease in mice and that our methods will provide a new animal model of Graves' disease.
机译:我们每两周用牛甲状腺球蛋白(Tg)免疫AKR / N小鼠,并监测它们在甲状腺中 125 I摄取活性的时间依赖性变化。 3个月后,来自经免疫小鼠的所有血清中的抗Tg抗体均为阳性。免疫小鼠(n = 6)的血清游离三碘甲状腺素(T3)和游离甲状腺素(T4)水平显着高于注射生理盐水(对照组)的小鼠(n = 6)。颈部计数和甲状腺闪烁显像显示,免疫小鼠的碘摄取活性并未受到抑制,但高于对照小鼠。六只免疫小鼠中的两只显示出极高的碘化物摄取活性。这两只小鼠的甲状腺弥漫性扩大,上皮细胞的高度也增加了。另外,两只具有高碘摄取活性的小鼠产生了高滴度的甲状腺刺激抗体。其他实验表明,用Tg免疫的11只AKR / N小鼠中有4只和10只C57BL6小鼠中有3只具有较高的血清无血清T3 /游离T4水平,甲状腺的高 125 I摄取活性和阳性甲状腺刺激性抗体活性。弥漫性甲状腺肿,甲状腺毒症,高碘摄取活性和甲状腺刺激性抗体阳性是Graves病的特征。因此,这些小鼠表现出格雷夫斯氏病的症状。这些结果表明,用Tg免疫可在小鼠中诱发Graves样疾病,并且我们的方法将提供Graves病的新动物模型。

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