Zabay J M, Fontán G, Campos A, García-Rodriguez M C, Pascual-Salcedo D, Bootello A, de la Concha E G
Clin Exp Immunol. 1984 Apr;56(1):23-8.
Three patients with the Wiskott-Aldrich syndrome were studied. One of them had no past history of relevant infections. The other two presented different degrees of humoral and cellular immunodeficiency and their T cells in vitro showed a defect in regulatory activity of Ig production in PWM stimulated cultures. This defect was not observed in the third patient. All three had normal numbers of B cells, producing normal amounts of Ig in vitro when co-cultured with normal T cells. It is suggested that the immunoregulatory T cell abnormality might play an important role in the pathogenesis of the humoral immunodeficiency.
对三名患有威斯科特-奥尔德里奇综合征的患者进行了研究。其中一名患者既往无相关感染史。另外两名患者表现出不同程度的体液免疫和细胞免疫缺陷,他们的T细胞在体外经PWM刺激培养时显示出Ig产生调节活性存在缺陷。第三名患者未观察到这种缺陷。三名患者的B细胞数量均正常,与正常T细胞共培养时在体外产生正常量的Ig。提示免疫调节性T细胞异常可能在体液免疫缺陷的发病机制中起重要作用。