Panaro M A, Panunzio M, Jirillo E, Marangi A, Brandonisio O
Istituto di Anatomia Umana Normale, University of Bari, Medical School, Italy.
Immunopharmacol Immunotoxicol. 1995 Aug;17(3):595-605. doi: 10.3109/08923979509016390.
Protozoan parasites of the Leishmania genus are the causative agents of important diseases in humans and animals. During their life cycle in vertebrate hosts, protozoa are able to live and proliferate within phagolysosomes of host phagocytic cells. The capacity to live in this hostile environment is likely due to the cell surface glycoconjugate expression. In particular, lipophosphoglycan (LPG), a major surface glycoconjugate of Leishmania promastigotes, has been reported to play an active role in protecting parasites within phagolysosomes via the impairment of killing mechanisms. In this review, the authors emphasize some novel LPG-mediated escape mechanisms of promastigotes from human phagocyte responses, such as the impairment of oxidative burst and of chemotactic activity. In the light of these findings, the knowledge of biological actions of LPG may be useful in order to prepare a vaccine against human leishmaniasis, using LPG defective avirulent mutant strains.
利什曼原虫属的原生动物寄生虫是人和动物重要疾病的病原体。在脊椎动物宿主的生命周期中,原生动物能够在宿主吞噬细胞的吞噬溶酶体内生存和增殖。能够在这种恶劣环境中生存可能归因于细胞表面糖缀合物的表达。特别是,脂磷壁酸(LPG)是利什曼原鞭毛体的主要表面糖缀合物,据报道它通过损害杀伤机制在保护吞噬溶酶体内的寄生虫方面发挥积极作用。在这篇综述中,作者强调了原鞭毛体从人类吞噬细胞反应中逃脱的一些新的LPG介导机制,如氧化爆发和趋化活性的损害。鉴于这些发现,LPG的生物学作用知识可能有助于制备针对人类利什曼病的疫苗,使用LPG缺陷的无毒突变株。