de Silva H J, Senanayake N
Department of Medicine, Faculty of Medicine, University of Peradeniya, Sri Lanka.
Southeast Asian J Trop Med Public Health. 1994 Dec;25(4):707-9.
Immunological mechanisms have been implicated in the pathogenesis of delayed cerebellar ataxia following falciparum malaria (DCA). We tested serum and CSF samples obtained from 39 Sri Lankan patients with DCA for the presence of antibodies (Ab) directed against cerebellar Purkinje cells by an immunofluorescence (IF) technique and Western blot analysis. For the IF test 7 mu thick frozen sections of histologically normal cerebellum obtained at post mortem were used. Proteins obtained from crude preparations of Purkinje cells isolated from the cerebellum were used for Western blot analysis. Sera obtained from patients known to have antineuronal antibodies associated with cerebellar degenerations and paraneoplastic disorders (anti-Hu and anti-Yo Ab) and sera from normal blood donors served as positive and negative controls, respectively. All serum and CSF samples obtained from patients with DCA were negative for Ab directed against cerebellar Purkinje cells. Humoral mechanisms are, therefore, unlikely to be important in the pathogenesis of this delayed complication of falciparum malaria.
免疫机制被认为与恶性疟原虫感染后迟发性小脑共济失调(DCA)的发病机制有关。我们通过免疫荧光(IF)技术和蛋白质印迹分析,检测了39例斯里兰卡DCA患者的血清和脑脊液样本中是否存在针对小脑浦肯野细胞的抗体(Ab)。IF检测使用了死后获得的组织学正常小脑的7微米厚冰冻切片。从小脑分离的浦肯野细胞粗提物中获得的蛋白质用于蛋白质印迹分析。已知患有与小脑变性和副肿瘤性疾病相关的抗神经元抗体(抗Hu和抗Yo抗体)的患者血清以及正常献血者的血清分别作为阳性和阴性对照。从DCA患者获得的所有血清和脑脊液样本中,针对小脑浦肯野细胞的抗体均为阴性。因此,体液机制在这种恶性疟原虫感染的迟发性并发症的发病机制中不太可能起重要作用。