Mitchell G F, Handman E
Walter and Eliza Hall Institute of Medical Research, Melbourne, Victoria, Australia.
Immunol Cell Biol. 1987 Oct;65 Pt 5:387-92. doi: 10.1038/icb.1987.44.
Mice immunized with a glycolipid antigen (GL) of Leishmania major plus adjuvant are relatively resistant to subsequent infection with this protozoan parasite. The GL is affinity purified on the monoclonal antibody WIC-79.3 which is L. major-specific and does not react with L. donovani. When another monoclonal, WIC-108.3, which cross-reacts with several Leishmania species, is used to affinity purify GL from L. donovani, the eluted material can partially protect genetically resistant mice against L. major. Thus, GL cross-reactions may in part underlie the known protective effects of crude L. donovani antigens against L. major infection. Experiments with live parasites of the L. major isolate LRC-L119, that is non-pathogenic in mice, that does not survive long in macrophages in vitro, and that has not been shown to contain any WIC-79.3 reactive GL, indicated that this isolate will very effectively protect mice against subsequent infection. This raises the possibility that GL is only one of at least two different classes of vaccinating antigen capable of protectively immunizing mice in this cutaneous leishmaniasis model.
用硕大利什曼原虫的糖脂抗原(GL)加佐剂免疫的小鼠对随后感染这种原生动物寄生虫具有相对抗性。该GL在单克隆抗体WIC - 79.3上进行亲和纯化,WIC - 79.3是硕大利什曼原虫特异性的,不与杜氏利什曼原虫反应。当使用与几种利什曼原虫物种发生交叉反应的另一种单克隆抗体WIC - 108.3从杜氏利什曼原虫中亲和纯化GL时,洗脱物可以部分保护基因抗性小鼠免受硕大利什曼原虫感染。因此,GL交叉反应可能部分是杜氏利什曼原虫粗抗原对硕大利什曼原虫感染已知保护作用的基础。对硕大利什曼原虫分离株LRC - L119的活寄生虫进行的实验表明,该分离株在小鼠中无致病性,在体外巨噬细胞中存活时间不长,且未显示含有任何与WIC - 79.3反应的GL,但它能非常有效地保护小鼠免受随后的感染。这增加了一种可能性,即GL只是在这种皮肤利什曼病模型中能够对小鼠进行保护性免疫的至少两类不同疫苗抗原之一。