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棘球蚴病

Echinococcosis.

作者信息

Taratuto A L, Venturiello S M

机构信息

Department of Neuropathology, Raul Carrea Institute for Neurological Research, Buenos Aires, Argentina.

出版信息

Brain Pathol. 1997 Jan;7(1):673-9. doi: 10.1111/j.1750-3639.1997.tb01082.x.

Abstract

Echinococcosis is a human disease caused by the larval form of Taenia echinococcus, which lives in the gut of the dog, wild canides and other carnivorous animals which represent the definitive hosts and involves as intermediate hosts both domestic and wild animals. Humans become accidental intermediate hosts by ingesting Taenia eggs. The main species pathogenic for man are E granulosus causing cystic echinococcosis with worldwide distribution and endemic in sheep and cattle breeding countries, and E multilocularis causing alveolar echinococcosis, with preferential distribution in the northern hemisphere. After ingestion of contaminated food, hexacanth embryos migrate by the portal system to liver and later lung, brain and other tissues. Symptoms are related to both cyst location and size. E granulosus infection of the central nervous system (CNS) may be primary or secondary and has been estimated to be low (2%). Sharply demarcated, spherical and intraparenchymal, cysts may reach a large size causing neurological symptoms. Spilling of cyst fluid due to trauma or surgery may trigger anaphylaxis as well as disseminated infection. Host reaction is minimal in the brain but a foreign giant cell reaction may develop. E multilocularis develops within the liver as a rapid invasive pseudomalignant growth and may metastasize to the CNS, where estimated incidence reaches 5%. Hydatid antigens induce an immune reaction in the host which is helpful for the diagnosis. DNA probes and PCR may be applied to differentiate between Echinococcus spp. Although the host develops an immunological protection from reinfection, the parasite evades host immune attack. A wide range of evasion mechanisms have been advanced, including a barrier for host cells due to hydatid cyst laminated cuticle, polyclonal activation of lymphocytes by parasite soluble antigens, and depression of host cell immune responses. Chronic stimulation of the host by cyst fluid antigens leads to increased specific IgG4 production, which might act as blocking antibodies against anaphlaxis suggestive of host response immunomodulation.

摘要

棘球蚴病是一种由细粒棘球绦虫幼虫引起的人类疾病,细粒棘球绦虫寄生于狗、野生犬科动物和其他食肉动物的肠道内,这些动物是终宿主,而家畜和野生动物则作为中间宿主。人类因摄入棘球绦虫卵而成为意外中间宿主。对人类致病的主要种类有引起囊型棘球蚴病的细粒棘球绦虫,该病在全球范围内分布,在绵羊和牛养殖国家呈地方性流行;以及引起泡型棘球蚴病的多房棘球绦虫,主要分布在北半球。摄入受污染食物后,六钩蚴通过门静脉系统迁移至肝脏,随后到达肺、脑和其他组织。症状与囊肿的位置和大小有关。细粒棘球绦虫感染中枢神经系统(CNS)可能是原发性的,也可能是继发性的,据估计感染率较低(2%)。界限清晰、球形且位于脑实质内的囊肿可能会长得很大,从而引起神经症状。因外伤或手术导致囊肿液外溢可能引发过敏反应以及播散性感染。宿主在脑内的反应很轻微,但可能会出现异物巨细胞反应。多房棘球绦虫在肝脏内呈快速侵袭性假恶性生长,并可能转移至中枢神经系统,据估计其发病率可达5%。棘球蚴抗原可诱导宿主产生免疫反应,这有助于诊断。DNA探针和聚合酶链反应(PCR)可用于区分棘球绦虫的种类。尽管宿主会产生免疫保护以防止再次感染,但寄生虫仍能逃避宿主的免疫攻击。人们提出了多种逃避机制,包括棘球蚴囊肿分层角质层对宿主细胞的屏障作用、寄生虫可溶性抗原对淋巴细胞的多克隆激活以及宿主细胞免疫反应的抑制。囊肿液抗原对宿主的慢性刺激会导致特异性IgG4产生增加,这可能作为针对过敏反应的阻断抗体,提示宿主反应的免疫调节。

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