Department of Microbiology & Immunology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, 955 Main Street, Buffalo, NY 14203.
Bioessays. 2018 Dec;40(12):e1800181. doi: 10.1002/bies.201800181. Epub 2018 Oct 29.
The process of antigenic variation in parasitic African trypanosomes is a remarkable mechanism for outwitting the immune system of the mammalian host, but it requires a delicate balancing act for the monoallelic expression, folding and transport of a single variant surface glycoprotein (VSG). Only one of hundreds of VSG genes is expressed at time, and this from just one of ≈15 dedicated expression sites. By switching expression of VSGs the parasite presents a continuously shifting antigenic facade leading to prolonged chronic infections lasting months to years. The basics of VSG structure and switching have been known for several decades, but recent studies have brought higher resolution to many aspects this process. New VSG structures, in silico modeling of infections, studies of VSG codon usage, and experimental ablation of VSG expression provide insights that inform how this remarkable system may have evolved.
寄生的非洲锥虫的抗原变异过程是一种巧妙的逃避哺乳动物宿主免疫系统的机制,但它需要微妙的平衡,以实现单等位基因表达、折叠和转运单一变异表面糖蛋白(VSG)。在任何时候,只有数百个 VSG 基因中的一个表达,而且这只是来自大约 15 个专用表达位点中的一个。通过切换 VSG 的表达,寄生虫呈现出不断变化的抗原表面,导致持续的慢性感染,持续数月至数年。VSG 结构和切换的基础知识已经存在了几十年,但最近的研究使这个过程的许多方面都有了更高的分辨率。新的 VSG 结构、感染的计算机模拟、VSG 密码子使用的研究以及 VSG 表达的实验消融提供了深入了解这个非凡系统是如何进化的。