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改良的肝包虫病实验模型,类似于自然感染途径,具有稳定的生长动态和免疫反应。

Improved experimental model of hepatic cystic hydatid disease resembling natural infection route with stable growing dynamics and immune reaction.

机构信息

Hepatobiliary and Hydatid Department, Digestive and Vascular Surgery Centre, Xinjiang Key Laboratory of Echinococcosis, The First Affiliated Hospital of Xinjiang Medical University, Urumqi 830011, Xinjiang Uygur Autonomous Region, China.

Department of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital, Zhejiang University, Hangzhou 310000, Zhejiang Province, China.

出版信息

World J Gastroenterol. 2017 Dec 7;23(45):7989-7999. doi: 10.3748/wjg.v23.i45.7989.

Abstract

AIM

To investigate a safer way to set up the disease model of cystic echinococcosis without contamination risk and develop a novel experimental murine model of hepatic cystic echinococcosis.

METHODS

C57B/6 mice were injected with human protoscolices of three different concentrations the portal vein. The mice were followed for 10 mo by ultrasound, gross anatomy, and pathological and immunological examinations. The protoscolex migration in the portal vein, hydatid cyst growth, host immune reaction, and hepatic histopathology were examined periodically.

RESULTS

The infection rates in the mice in the high, medium, and low concentration groups were 90%, 100%, and 63.6%, respectively. The protoscolices migrated in the portal vein with blood flow, settled in the liver, and developed into orthotopic hepatic hydatid cysts, resembling the natural infection route and course.

CONCLUSION

We have established an improved experimental model of hepatic cystic echinococcosis with low biohazard risk but stable growing dynamics and immune reaction. It is especially useful for new anti-parasite medication trials against hydatid disease.

摘要

目的

探索一种更安全的方法来建立无污染风险的包虫病模型,并开发一种新型实验性肝包虫病小鼠模型。

方法

经门静脉向 C57B/6 小鼠注入三种不同浓度的人原头蚴。通过超声、大体解剖、病理和免疫检查对小鼠进行 10 个月的随访。定期检查原头蚴在门静脉中的迁移、包虫囊肿的生长、宿主免疫反应和肝组织病理学变化。

结果

高、中、低浓度组小鼠的感染率分别为 90%、100%和 63.6%。原头蚴随血流迁移至门静脉,在肝脏内定居并发育为原位肝包虫囊肿,类似于自然感染途径和过程。

结论

我们建立了一种具有低生物危害风险但生长动态和免疫反应稳定的改良实验性肝包虫病模型。它特别适用于新的抗包虫病药物对包虫病的试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c92c/5725293/ce68e9a55d79/WJG-23-7989-g001.jpg

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