Freedman D O, Lujan-Trangay A, Steel C, Gonzalez-Peralta C, Nutman T B
Clinical Parasitology Section, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.
J Clin Invest. 1991 Jul;88(1):231-8. doi: 10.1172/JCI115282.
To help define the immunoregulatory defects in patients with onchocerciasis, flow cytometric analysis of circulating lymphocyte subpopulations was performed in parallel with functional assays. No significant differences in CD4/CD8 ratios were seen when microfilariae-positive individuals from Guatemala were compared with Guatemalan controls. However, the infected individuals had significantly increased numbers of circulating CD4+CD45RA+ lymphocytes (mean 38.3%) when compared with controls (mean 16.0%). Coexpression of the activation marker HLA-DR was significantly increased on CD4+ cells from infected individuals. In contrast, no up-regulation of HLA-DR was seen on CD8+ or CD19+ cells. At 1 year after initiation of treatment with semiannual doses of the microfilaricide ivermectin, there were significant increases (P less than 0.05) in the percentage of CD4+CD45RA- cells, the percentage of CD4+HLA-DR+ cells, and mitogen-induced lymphokine production (IL-2, IL-4). Despite these changes, parasite-specific IL-2 and IL-4 production which had been undetectable before treatment did not manifest itself even by the 2-yr follow-up. Defects in the T-cell activation pathway in Onchocerca volvulus-infected individuals may thus exist at several independent points; a state of parasite antigen-specific tolerance appears to remain even after the relative reversal of other generalized immunoregulatory defects.
为了明确盘尾丝虫病患者的免疫调节缺陷,我们同时进行了循环淋巴细胞亚群的流式细胞术分析和功能检测。将危地马拉的微丝蚴阳性个体与危地马拉对照组进行比较时,未发现CD4/CD8比值有显著差异。然而,与对照组(平均16.0%)相比,感染个体的循环CD4+CD45RA+淋巴细胞数量显著增加(平均38.3%)。感染个体CD4+细胞上激活标记物HLA-DR的共表达显著增加。相比之下,CD8+或CD19+细胞上未观察到HLA-DR的上调。在用微丝蚴杀虫剂伊维菌素半年度剂量治疗1年后,CD4+CD45RA-细胞百分比、CD4+HLA-DR+细胞百分比以及丝裂原诱导的淋巴因子产生(IL-2、IL-4)均显著增加(P小于0.05)。尽管有这些变化,但治疗前无法检测到的寄生虫特异性IL-2和IL-4产生即使在2年随访时也未表现出来。因此,盘尾丝虫感染个体的T细胞激活途径可能在几个独立点存在缺陷;即使在其他全身性免疫调节缺陷相对逆转后,寄生虫抗原特异性耐受状态似乎仍然存在。