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抗肝吸虫实验疫苗的研发

Development of Experimental Vaccines Against Liver Flukes.

作者信息

Yap Huan Yong, Smooker Peter M

机构信息

School of Applied Sciences, RMIT University, Plenty Road, Bundoora, VIC, 3083, Australia.

出版信息

Methods Mol Biol. 2016;1404:135-151. doi: 10.1007/978-1-4939-3389-1_9.

Abstract

A multitude of experimental vaccines have been developed against liver flukes in the past. However, there has yet to be the development of a commercial livestock vaccine. Reasons for this may be multiple, and include the lack of identification of the best antigen(s), or the immune response induced by those antigens not being appropriate in either magnitude or polarity (and therefore not protective). Cathepsin proteases are the major component of the excretory/secretory (ES) material of liver flukes in all stages of their life cycle in the definitive host and are the primary antigens of interest for the vaccine development in many studies. Hence, this chapter presents the methodologies of using cathepsin proteases as targeted antigens in recombinant protein and DNA vaccine development to engender protective immune responses against fasciolosis.First, the experimental vaccines developed in the past and the criteria of an effective vaccine for fasciolosis are briefly reviewed. Then flowcharts for recombinant protein vaccine and DNA vaccine development are presented, followed by the detailed materials and methodologies.

摘要

过去已经研发出多种针对肝吸虫的实验性疫苗。然而,尚未有商业化的家畜疫苗问世。原因可能是多方面的,包括尚未确定最佳抗原,或者这些抗原诱导的免疫反应在强度或极性方面不合适(因此没有保护性)。组织蛋白酶是肝吸虫在终末宿主体内生命周期各阶段排泄/分泌(ES)物质的主要成分,并且是许多研究中疫苗研发的主要关注抗原。因此,本章介绍了在重组蛋白和DNA疫苗研发中使用组织蛋白酶作为靶向抗原以产生针对肝片吸虫病的保护性免疫反应的方法。首先,简要回顾过去研发的实验性疫苗以及肝片吸虫病有效疫苗的标准。然后给出重组蛋白疫苗和DNA疫苗研发的流程图,随后是详细的材料和方法。

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