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基因编辑的时机:新一代减毒疟原虫。

Time for Genome Editing: Next-Generation Attenuated Malaria Parasites.

机构信息

Integrative Parasitology, Center for Infectious Diseases, University of Heidelberg Medical School, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany.

出版信息

Trends Parasitol. 2017 Mar;33(3):202-213. doi: 10.1016/j.pt.2016.09.012. Epub 2016 Oct 25.

Abstract

Immunization with malaria parasites that developmentally arrest in or immediately after the liver stage is the only way currently known to confer sterilizing immunity in both humans and rodent models. There are various ways to attenuate parasite development resulting in different timings of arrest, which has a significant impact on vaccination efficiency. To understand what most impacts vaccination efficiency, newly developed gain-of-function methods can now be used to generate a wide array of differently attenuated parasites. The combination of multiple attenuation approaches offers the potential to engineer efficiently attenuated Plasmodium parasites and learn about their fascinating biology at the same time. Here we discuss recent studies and the potential of targeted parasite manipulation using genome editing to develop live attenuated malaria vaccines.

摘要

用在肝期发育停滞或刚进入肝期的疟原虫免疫是目前已知的唯一能在人类和啮齿动物模型中产生绝育免疫的方法。有多种方法可以减弱寄生虫的发育,从而导致不同的停滞时间,这对疫苗的效率有重大影响。为了了解什么对疫苗效率的影响最大,现在可以使用新开发的功能获得方法来产生广泛的不同减毒寄生虫。多种减毒方法的结合有可能有效地设计减毒疟原虫,并同时了解其迷人的生物学特性。在这里,我们讨论了最近的研究以及使用基因组编辑进行靶向寄生虫操作的潜力,以开发减毒活疟疾疫苗。

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