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Therapeutic effects of Echinococcus granulosus cystic fluid on allergic airway inflammation.
Kim, Hye-Jin; Kang, Shin-Ae; Yong, Tai-Soon; Shin, Myeong-Heon; Lee, Kyu-Jae; Park, Gab-Man; Suvonkulov, Uktamjon; Yu, Hak Sun.
Afiliación
  • Kim HJ; 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.
  • Kang SA; 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.
  • Yong TS; Department of Environmental Medical Biology, Institute of Tropical Medicine, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
  • Shin MH; Department of Environmental Medical Biology, Institute of Tropical Medicine, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
  • Lee KJ; Department of Environmental Medical Biology, Yonsei University Wonju College of Medicine, Wonju, 26426, Republic of Korea.
  • Park GM; Department of Environmental Medical Biology, Catholic Kwandong University College of Medicine, Gangneung, 25601, Republic of Korea.
  • Suvonkulov U; Isaev Research Institute of Medical Parasitology, Ministry of Health, Republic of Uzbekistan.
  • Yu HS; 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. Electronic address: hsyu@pusan.ac.kr.
Exp Parasitol ; 198: 63-70, 2019 Mar.
Article en En | MEDLINE | ID: mdl-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 (CD4+CD25+Foxp3+T, 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-4+CD4+ 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Líquido del Lavado Bronquioalveolar / Resistencia de las Vías Respiratorias / Líquido Quístico / Echinococcus granulosus / Hipersensibilidad Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Exp Parasitol Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Líquido del Lavado Bronquioalveolar / Resistencia de las Vías Respiratorias / Líquido Quístico / Echinococcus granulosus / Hipersensibilidad Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Exp Parasitol Año: 2019 Tipo del documento: Article