Donelson J E, Hill K L, El-Sayed N M
Department of Biochemistry, University of Iowa, Iowa City 52242, USA.
Mol Biochem Parasitol. 1998 Mar 1;91(1):51-66. doi: 10.1016/s0166-6851(97)00209-0.
During infection of a mammalian host, African trypanosomes are in constant contact with the host's immune system. These protozoan parasites are infamous for their ability to evade the immune responses by periodically switching their major variant surface glycoprotein (VSG), a phenomenon called antigenic variation. Antigenic variation, however, is likely to be only one of several mechanisms enabling these organisms to thrive in the face of the immune defenses. The ability to grow in high levels of interferon-gamma (IFN-gamma) and to avoid complement-mediated destruction may also facilitate the parasite's survival. In this review we summarize (i) the activation of trypanosome genes for three different VSGs during antigenic variation, (ii) the secretion of a trypanosome protein that induces host CD8 T cells to produce IFN-gamma, and (iii) the evidence for trypanosome protein similar to a surface protease of Leishmania that plays a role in resistance to complement-mediated lysis.
在感染哺乳动物宿主期间,非洲锥虫不断与宿主的免疫系统接触。这些原生动物寄生虫以其通过周期性切换主要可变表面糖蛋白(VSG)来逃避免疫反应的能力而臭名昭著,这种现象称为抗原变异。然而,抗原变异可能只是使这些生物体在免疫防御面前茁壮成长的几种机制之一。在高水平干扰素-γ(IFN-γ)中生长以及避免补体介导的破坏的能力也可能促进寄生虫的存活。在这篇综述中,我们总结了:(i)抗原变异期间三种不同VSG的锥虫基因的激活;(ii)一种诱导宿主CD8 T细胞产生IFN-γ的锥虫蛋白的分泌;以及(iii)与利什曼原虫表面蛋白酶相似的锥虫蛋白在抵抗补体介导的裂解中起作用的证据。