Grove D I, O'Callaghan S J, Burston T O, Forbes I J
Br Med J. 1973 Jul 14;3(5871):81-3. doi: 10.1136/bmj.3.5871.81.
Humoral and cellular immunity have been investigated in 15 patients with dystrophia myotonica. No abnormalities in total serum levels of the five major immunoglobulin classes were found but there was a rise in the mean serum level of beta(1)A complement. Altogether, 54% of patients failed to make antibody to tetanus toxoid as compared with 1% of controls: 13% of patients failed to make antibody to Salmonella typhi H antigen as compared with no failure of this function in control subjects. There was a reduced uptake of tritiated thymidine by whole blood lymphocyte cultures spontaneously, while in the presence of phytohaemagglutinin (PHA) and both autologous and fetal calf serum the uptake was normal. It is suggested that there may be a wider derangement of immunological function in dystrophia myotonica than previously thought.
对15例强直性肌营养不良患者的体液免疫和细胞免疫进行了研究。未发现五种主要免疫球蛋白类别的血清总水平有异常,但β(1)A补体的平均血清水平有所升高。总体而言,54%的患者对破伤风类毒素不产生抗体,而对照组为1%;13%的患者对伤寒杆菌H抗原不产生抗体,而对照组该功能无缺失。全血淋巴细胞培养自发摄取氚标记胸腺嘧啶核苷减少,而在存在植物血凝素(PHA)以及自体和胎牛血清的情况下摄取正常。提示强直性肌营养不良患者的免疫功能紊乱可能比以前认为的更广泛。