Department of Microbiology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Raibareli Road, Lucknow 226014, India.
Exp Parasitol. 2011 Mar;127(3):687-92. doi: 10.1016/j.exppara.2010.11.006. Epub 2010 Nov 26.
The immunopathogenesis of neurocysticercosis (NCC) largely remains unknown. We analyzed the immune response to different fractions of Taenia solium cyst fluid antigens in patients with NCC. Lymphocytes were separated from 48 patients with NCC-related active epilepsy and 30 healthy controls. T. solium (isolated from pig muscles) antigens (crude lysate, CL; cyst wall, CW and cyst fluid, CF) at 20 μg/well concentrations were used to stimulate the cells in a lymphocyte transformation test (LTT). Only CF antigen stimulated cell proliferation significantly greater than control (p<0.001), hence cyst fluid antigens were further studied. The CF antigens were electro-blotted on nitrocellulose membrane (NC), cut at 0.5 cm distance and particulate antigens were prepared. A total of 12 fractions, designated F1 to F12 according to molecular weight were tested in-vitro for LTT. After 72 h of stimulation by the different fractions, Th1 (IL-1β, TNF-α, IL-2) and Th2 (IL-4, IL-10) cytokine responses were determined in culture supernatants by ELISA. Low molecular weight fractions F1 through F4 (Mol. wt.<25 kDa) were found to be potent inducers of cytokines. Fractions F1, F3 and F4 induced the production of Th1 (IL-1β, TNF-α, IL-2), whereas F2 induced the production of Th2 (IL-4 and IL-10) cytokine. The study shows that the low molecular weight fractions of CF antigens are immuno-dominant. Most of these fractions (F1, F3, F4) induce strong Th1 immune response except F2 which induces Th2 response. Further studies are needed to identify the different antigens present in these fractions to determine the molecules responsible for the immune response.
神经囊尾蚴病(NCC)的免疫发病机制在很大程度上仍然未知。我们分析了 NCC 患者对不同猪带绦虫囊液抗原片段的免疫反应。从 48 例 NCC 相关活动性癫痫患者和 30 例健康对照者中分离淋巴细胞。用 20μg/孔浓度的猪带绦虫(从猪肌肉中分离)抗原(粗裂解物,CL;囊壁,CW 和囊液,CF)在淋巴细胞转化试验(LTT)中刺激细胞。只有 CF 抗原刺激细胞增殖显著大于对照(p<0.001),因此进一步研究囊液抗原。CF 抗原在硝酸纤维素膜(NC)上电泳,每隔 0.5cm 切开,制备颗粒性抗原。根据分子量将 CF 抗原分为 12 个部分,分别命名为 F1 到 F12,并在体外进行 LTT 检测。用不同部分刺激 72 小时后,通过 ELISA 在培养上清液中测定 Th1(IL-1β、TNF-α、IL-2)和 Th2(IL-4、IL-10)细胞因子反应。发现低分子量部分 F1 到 F4(Mol.wt.<25 kDa)是细胞因子的有效诱导剂。F1、F3 和 F4 诱导产生 Th1(IL-1β、TNF-α、IL-2)细胞因子,而 F2 诱导产生 Th2(IL-4 和 IL-10)细胞因子。该研究表明 CF 抗原的低分子量部分是免疫优势的。这些部分中的大多数(F1、F3、F4)诱导强烈的 Th1 免疫反应,除了 F2 诱导 Th2 反应。需要进一步研究以鉴定这些部分中存在的不同抗原,以确定负责免疫反应的分子。