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细粒棘球绦虫囊液对过敏性气道炎症的治疗作用

Therapeutic effects of Echinococcus granulosus cystic fluid on allergic airway inflammation.

作者信息

Kim Hye-Jin, Kang Shin-Ae, Yong Tai-Soon, Shin Myeong-Heon, Lee Kyu-Jae, Park Gab-Man, Suvonkulov Uktamjon, Yu Hak Sun

机构信息

Department of Parasitology, School of Medicine, Pusan National University, Yangsan-si, Gyeongsangnam-do, 626-870, Republic of Korea; Immunoregulatory Therapeutics Group in Brain Busan 21 Project, Republic of Korea.

Department of Environmental Medical Biology, Institute of Tropical Medicine, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.

出版信息

Exp Parasitol. 2019 Mar;198:63-70. doi: 10.1016/j.exppara.2019.02.003. Epub 2019 Feb 11.

DOI:10.1016/j.exppara.2019.02.003
PMID:30763570
Abstract

Previous studies showed that Echinococcus granulosus infection reduces allergic airway inflammation in experimentally infected hosts and the cystic fluid of E. granulosus is known to activate regulatory T (CD4CD25Foxp3T, Treg) cells. To evaluate the effects of cystic fluid of E. granulosus on allergic airway inflammation, we investigated the regulation of the inflammatory reaction by cystic fluid using an allergic airway inflammation animal model. Cystic fluid was administered to C57BL/6 mice seven times every other day, after which allergic airway inflammation was induced using ovalbumin and aluminum. The airway resistance, number of eosinophils and other immune cells in the bronchoalveolar lavage fluid, and levels of Th2 and Th17-related cytokines were significantly reduced by cystic fluid pre-treatment in allergic airway inflammation-induced mice. The number IL-4CD4 T cells decreased, the number of Treg cells increased in the lung-draining lymph nodes and spleen of cystic fluid pre-treated mice. In conclusion, E. granulosus-derived cystic fluid may alleviate the Th2 allergic airway inflammatory response via Treg cells. Further studies of the immune regulation of cystic fluid may lead to the development of therapeutic agents for immune disorders.

摘要

先前的研究表明,细粒棘球绦虫感染可减轻实验性感染宿主的过敏性气道炎症,且已知细粒棘球绦虫的囊液可激活调节性T(CD4CD25Foxp3T,Treg)细胞。为评估细粒棘球绦虫囊液对过敏性气道炎症的影响,我们使用过敏性气道炎症动物模型研究了囊液对炎症反应的调节作用。每隔一天给C57BL/6小鼠注射7次囊液,之后用卵清蛋白和铝诱导过敏性气道炎症。在诱导过敏性气道炎症的小鼠中,囊液预处理可显著降低气道阻力、支气管肺泡灌洗液中嗜酸性粒细胞及其他免疫细胞的数量,以及Th2和Th17相关细胞因子的水平。囊液预处理小鼠的肺引流淋巴结和脾脏中,IL-4CD4 T细胞数量减少,Treg细胞数量增加。总之,细粒棘球绦虫来源的囊液可能通过Treg细胞减轻Th2过敏性气道炎症反应。对囊液免疫调节的进一步研究可能会促成免疫紊乱治疗药物的开发。

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