Odds Frank C, Brown Alistair J P, Gow Neil A R
Aberdeen Fungal Group, University of Aberdeen, Department of Molecular and Cell Biology, Institute of Medical Sciences, Aberdeen AB25 2ZD, UK.
Trends Microbiol. 2003 Jun;11(6):272-9. doi: 10.1016/s0966-842x(03)00117-3.
Clinical needs for novel antifungal agents have altered steadily with the rise and fall of AIDS-related mycoses, and the change in spectrum of fatal disseminated fungal infections that has accompanied changes in therapeutic immunosuppressive therapies. The search for new molecular targets for antifungals has generated considerable research using modern genomic approaches, so far without generating new agents for clinical use. Meanwhile, six new antifungal agents have just reached, or are approaching, the clinic. Three are new triazoles, with extremely broad antifungal spectra, and three are echinocandins, which inhibit synthesis of fungal cell wall polysaccharides--a new mode of action. In addition, the sordarins represent a novel class of agents that inhibit fungal protein synthesis. This review describes the targets and mechanisms of action of all classes of antifungal agents in clinical use or with clinical potential.
随着与艾滋病相关的真菌病的起伏,以及致命播散性真菌感染谱的变化(这与治疗性免疫抑制疗法的变化相伴),对新型抗真菌药物的临床需求一直在稳步改变。利用现代基因组学方法寻找抗真菌药物新分子靶点的研究已开展了很多,但至今尚未产生可用于临床的新药物。与此同时,六种新型抗真菌药物刚刚进入或即将进入临床。三种是新型三唑类药物,具有极其广泛的抗真菌谱,另外三种是棘白菌素类药物,可抑制真菌细胞壁多糖的合成——这是一种新的作用方式。此外,嗜球果伞素代表了一类新型的抑制真菌蛋白质合成的药物。本综述描述了所有临床使用的或具有临床潜力的抗真菌药物的靶点和作用机制。