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肠道蠕虫感染的免疫病理学

Immunopathology of intestinal helminth infection.

作者信息

Garside P, Kennedy M W, Wakelin D, Lawrence C E

机构信息

Department of Immunology and Bacteriology, University of Glasgow, Western Infirmary, Glasgow, UK.

出版信息

Parasite Immunol. 2000 Dec;22(12):605-12. doi: 10.1046/j.1365-3024.2000.00344.x.

DOI:10.1046/j.1365-3024.2000.00344.x
PMID:11123752
Abstract

The relationship between intestinal pathology and immune expulsion of gastrointestinal nematodes remains controversial. Parasite expulsion is associated with intestinal pathology in several model systems and both of these phenomena are T cell dependent. However, while immune expulsion of gastrointestinal helminth parasites is usually associated with Th2 responses, the effector mechanisms directly responsible for parasite loss have not been elucidated. In contrast, the intestinal pathology observed in many other disease models closely resembles that seen in helminth infections, but has been attributed to Th1 cytokines. We have used infection with the nematode Trichinella spiralis in mice defective for cytokines to demonstrate that although parasite expulsion is indeed IL-4 dependent, contrary to expectations, the enteropathy is also regulated by IL-4. Furthermore, abrogation of severe pathology in iNOS deficient and TNF receptor defective animals does not prevent parasite expulsion. TNF and iNOS are therefore involved in intestinal pathology in nematode infections, apparently under regulation by IL-4 and Th2 mediated responses. Therefore, it appears that the IL-4-dependent protective response against the parasite operates by a mechanism other than merely the gross degradation of the parasite's environment brought about by the immune enteropathy. However, it remains important to elucidate the protective mechanisms involved in parasite expulsion, which are still unclear.

摘要

肠道病理学与胃肠道线虫免疫清除之间的关系仍存在争议。在多个模型系统中,寄生虫清除与肠道病理学相关,且这两种现象均依赖于T细胞。然而,虽然胃肠道蠕虫寄生虫的免疫清除通常与Th2反应相关,但直接导致寄生虫清除的效应机制尚未阐明。相比之下,在许多其他疾病模型中观察到的肠道病理学与蠕虫感染中所见的非常相似,但却归因于Th1细胞因子。我们利用细胞因子缺陷小鼠感染旋毛虫线虫,以证明尽管寄生虫清除确实依赖于IL-4,但与预期相反,肠道病变也受IL-4调控。此外,在iNOS缺陷和TNF受体缺陷动物中消除严重病变并不能阻止寄生虫清除。因此,TNF和iNOS显然在IL-4和Th2介导的反应调控下参与线虫感染中的肠道病理学。因此,看来针对寄生虫的IL-4依赖性保护反应并非仅仅通过免疫性肠病导致寄生虫生存环境的总体破坏这一机制起作用。然而,阐明寄生虫清除所涉及的保护机制仍然很重要,目前这些机制尚不清楚。

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