Okabe N, Inoue K, Mori R
J Clin Lab Immunol. 1983 Feb;10(2):91-5.
To detect possible changes in the T lymphocyte subpopulations in patients with Graves' disease, T mu and T gamma lymphocytes and "active" T lymphocytes were counted in the peripheral blood lymphocytes. Antithyroid autoantibodies were also measured in correlation with T lymphocyte subset analysis. We found no alteration whatever in T lymphocyte subpopulations, although there was a slight increase in the proportion of "active" T lymphocytes and T gamma lymphocytes in the untreated group, as compared to treated group, but the difference was not statistically significant. There was no correlation between T lymphocyte subpopulations and antithyroid autoantibodies. These data indicate that the defects in T gamma lymphocytes with suppressor function, probably does not explain the etiology of Graves' disease, despite the hypothesis that defects in suppressor cells may lead to the production of thyroid stimulating immunoglobulins and antithyroid autoantibodies in Graves' disease.
为检测格雷夫斯病患者T淋巴细胞亚群的可能变化,对其外周血淋巴细胞中的Tμ和Tγ淋巴细胞以及“活性”T淋巴细胞进行了计数。还测定了抗甲状腺自身抗体,并与T淋巴细胞亚群分析相关联。我们发现T淋巴细胞亚群没有任何改变,尽管与治疗组相比,未治疗组中“活性”T淋巴细胞和Tγ淋巴细胞的比例略有增加,但差异无统计学意义。T淋巴细胞亚群与抗甲状腺自身抗体之间没有相关性。这些数据表明,尽管有假说认为抑制细胞缺陷可能导致格雷夫斯病中甲状腺刺激免疫球蛋白和抗甲状腺自身抗体的产生,但具有抑制功能的Tγ淋巴细胞缺陷可能无法解释格雷夫斯病的病因。