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一种用于疟疾的全寄生虫传播阻断疫苗:一种被忽视的策略。

A whole parasite transmission-blocking vaccine for malaria: an ignored strategy.

作者信息

Good Michael F, Yanow Stephanie K

机构信息

Institute for Glycomics, Griffith University, Gold Coast 4222, Australia.

School of Public Health, University of Alberta, Edmonton, Canada T6G 2E1.

出版信息

Emerg Top Life Sci. 2017 Dec 22;1(6):547-552. doi: 10.1042/ETLS20170117.

Abstract

Malaria vaccine approaches can be divided into 'subunit' and 'whole parasite', and these can be directed at the sporozoite, liver stage, asexual or sexual stages. All combinations of approach and stage are under development with the exception of a whole parasite sexual stage (gametocyte) vaccine. A gametocyte vaccine would aim primarily to block transmission of malaria from the human host to the mosquito vector and as such is referred to as a 'transmission-blocking vaccine'. An immunological feature of whole parasite vaccines for the sporozoite/liver stage and for the asexual blood stage is the reliance on cellular immunity involving T-cells to control parasite growth. T-cells can also respond vigorously to gametocytes and kill them in the vertebrate host and/or arrest their development. To date, cellular immunity has not been exploited in transmission-blocking vaccine development. Here, the data supporting a gametocyte whole parasite vaccine are reviewed and a strategy for vaccine development and testing is outlined.

摘要

疟疾疫苗的研发方法可分为“亚单位”和“全寄生虫”两类,且这些方法可针对子孢子、肝期、无性或有性阶段。除了全寄生虫有性阶段(配子体)疫苗外,其他所有方法和阶段的组合都在研发中。配子体疫苗的主要目标是阻断疟疾从人类宿主传播到蚊媒,因此被称为“传播阻断疫苗”。针对子孢子/肝期和无性血液期的全寄生虫疫苗的一个免疫学特征是依赖涉及T细胞的细胞免疫来控制寄生虫生长。T细胞也能对配子体产生强烈反应,并在脊椎动物宿主中杀死它们和/或阻止其发育。迄今为止,细胞免疫尚未被用于传播阻断疫苗的研发。在此,我们回顾了支持配子体全寄生虫疫苗的数据,并概述了疫苗研发和测试的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b9d/7289001/028cb2b9dcbe/ETLS-1-547-g0001.jpg

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