Barry J D, Crowe J S, Vickerman K
Nature. 1983;306(5944):699-701. doi: 10.1038/306699a0.
Trypanosoma brucei rhodesiense undergoes antigenic variation in its mammalian host by changing the glycoprotein composing its surface coat. Trypanosome clones which have the same repertoire of variable antigen types (VATs) are said to belong to the same serodeme. Tsetse flies infected with a particular serodeme extrude infective metacyclic trypanosomes which express only a restricted part of this repertoire. As the only known acquired immunity in African trypanosomiasis is VAT-specific this limitation of metacyclic VAT (M-VAT) repertoire could be important in devising a vaccine. This possibility of immunoprophylaxis could depend, however, on whether or not the M-VAT repertoire is conserved over long periods of repeated cyclical transmission and between epidemics. Studies reported here on isolates made from an East African focus of sleeping sickness over a 20-yr period suggest substantial changes in the M-VATs expressed during this time. Furthermore, we have detected change in expression of 3 M-VATs during sequential tsetse transmission of a clone in the laboratory indicating a possible instability in the organization of M-VAT genes.
布氏罗得西亚锥虫在其哺乳动物宿主体内通过改变构成其表面被膜的糖蛋白来进行抗原变异。具有相同可变抗原类型(VATs)库的锥虫克隆被认为属于同一血清型。感染特定血清型的采采蝇会排出仅表达该库中有限部分的感染性循环后期锥虫。由于非洲锥虫病中唯一已知的获得性免疫是VAT特异性的,循环后期VAT(M-VAT)库的这种限制在设计疫苗时可能很重要。然而,这种免疫预防的可能性可能取决于M-VAT库在长期反复循环传播期间以及不同流行期之间是否保守。此处报道的关于在20年期间从东非昏睡病疫源地分离出的菌株的研究表明,在此期间表达的M-VATs发生了重大变化。此外,我们在实验室中对一个克隆进行采采蝇连续传播期间检测到3种M-VATs的表达变化,这表明M-VAT基因的组织可能存在不稳定性。