Robinson P, Atmar R L, Lewis D E, White A C
Department of Microbiology & Immunology, Baylor College of Medicine, Houston, Texas 77030, USA.
Infect Immun. 1997 Jul;65(7):2925-31. doi: 10.1128/iai.65.7.2925-2931.1997.
Neurocysticercosis, caused by Taenia solium, is one of the most common causes of seizures worldwide. The symptoms result from granulomatous inflammation associated with dying cyst forms of the parasite. Although the invasive larvae can be killed by immune serum plus complement, immunity to the cyst stage depends on a cellular response. This dichotomous immune response is reminiscent of the extremes of the immune response associated with T helper 1 (Th1) and Th2 cytokine profiles. To characterize the cytokine response in cysticercosis, granulomas were removed from the peritoneal cavity of mice infected with Taenia crassiceps cysts and examined for cytokine message by in situ hybridization using 35S-labeled RNA probes. The granulomas were staged based on histologic appearance of the degenerating parasite. Message for gamma interferon (IFN-gamma) was identified by light microscopy in 11 of the 12 granulomas, and interleukin-2 (IL-2) message was identified in 9 of the 12. By laser scanning confocal microscopy, significantly increased IFN-gamma and IL-2 pixel intensity was identified in nearly all of the granulomas from early histologic stages. Message for IL-4 was seen in 6 of the 12 granulomas. Only granulomas with complete destruction of the parasite architecture displayed more than minimal amounts of IL-4 message by light microscopy, and only 2 of 12 granulomas had IL-4 pixel intensity significantly above background. Only minimal amounts of IL-10 message were detected in 4 of 11 granulomas. Thus, early granulomas in cysticercosis are predominantly associated with a Th1 response, whereas later granulomas, in which parasite destruction is complete, have a mixture of Th1 and IL-4. The Th1 response appears to play an important role both in the pathogenesis of disease as well as in the clearing of the parasites, with IL-4 involved in downregulation of the initial response.
由猪带绦虫引起的神经囊尾蚴病是全球癫痫发作最常见的病因之一。症状源于与寄生虫死亡囊肿形式相关的肉芽肿性炎症。虽然侵入性幼虫可被免疫血清加补体杀死,但对囊肿阶段的免疫取决于细胞反应。这种二分的免疫反应让人联想到与辅助性T细胞1(Th1)和Th2细胞因子谱相关的免疫反应的极端情况。为了表征囊尾蚴病中的细胞因子反应,从感染粗颈绦虫囊肿的小鼠腹腔中取出肉芽肿,并用35S标记的RNA探针通过原位杂交检测细胞因子信息。根据退化寄生虫的组织学外观对肉芽肿进行分期。通过光学显微镜在12个肉芽肿中的11个中鉴定出γ干扰素(IFN-γ)信息,在12个中的9个中鉴定出白细胞介素-2(IL-2)信息。通过激光扫描共聚焦显微镜,在几乎所有早期组织学阶段的肉芽肿中都发现IFN-γ和IL-2像素强度显著增加。在12个肉芽肿中的6个中发现了IL-4信息。只有寄生虫结构完全破坏的肉芽肿通过光学显微镜显示出超过微量的IL-4信息,并且12个肉芽肿中只有2个的IL-4像素强度显著高于背景。在11个肉芽肿中的4个中仅检测到微量的IL-10信息。因此,囊尾蚴病中的早期肉芽肿主要与Th1反应相关,而后期寄生虫破坏完全的肉芽肿则具有Th1和IL-4的混合反应。Th1反应似乎在疾病发病机制以及寄生虫清除中都起着重要作用,而IL-4参与初始反应的下调。