Wolf Philipp, Elsässer-Beile Ursula
Department of Urology, University of Freiburg, Germany.
Int J Med Microbiol. 2009 Mar;299(3):161-76. doi: 10.1016/j.ijmm.2008.08.003. Epub 2008 Oct 23.
The pathogenic bacterium Pseudomonas aeruginosa has the ability to cause severe acute and chronic infections in humans. Pseudomonas exotoxin A (PE) is the most toxic virulence factor of this bacterium. It has ADP-ribosylation activity and decisively affects the protein synthesis of the host cells. The cytotoxic pathways of PE have been elucidated, and it could be shown that PE uses several molecular strategies developed under evolutionary pressure for effective killing. Interestingly, a medical benefit from this molecule has also been ascertained in recent years and several PE-based immunotoxins have been constructed and tested in preclinical and clinical trials against different cancers. In these molecules, the enzymatic active domain of PE is specifically targeted to tumor-related antigens. This review describes the current knowledge about the cytotoxic pathways of PE. Additionally, it summarizes preclinical and clinical trials of PE-based immunotoxins and furthermore discusses current problems and answers with these agents.
病原菌铜绿假单胞菌能够在人类中引起严重的急性和慢性感染。铜绿假单胞菌外毒素A(PE)是该细菌毒性最强的毒力因子。它具有ADP核糖基化活性,对宿主细胞的蛋白质合成有决定性影响。PE的细胞毒性途径已得到阐明,结果表明PE采用了在进化压力下形成的几种分子策略来有效杀伤细胞。有趣的是,近年来人们还确定了该分子的医学益处,并且已经构建了几种基于PE的免疫毒素,并在针对不同癌症的临床前和临床试验中进行了测试。在这些分子中,PE的酶活性结构域特异性靶向肿瘤相关抗原。本综述描述了目前关于PE细胞毒性途径的知识。此外,总结了基于PE的免疫毒素的临床前和临床试验,并进一步讨论了这些药物目前存在的问题及应对方法。