Walsh T J, Viviani M A, Arathoon E, Chiou C, Ghannoum M, Groll A H, Odds F C
Immunocompromised Host Section, Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD 20892, USA.
Med Mycol. 2000;38 Suppl 1:335-47.
Development of new approaches for treatment of invasive fungal infections encompasses new delivery systems for approved and investigational compounds, as well as exploiting the cell membrane, cell wall and virulence factors as putative antifungal targets. Novel delivery systems consisting of cyclodextrins, cochleates, nanoparticles/nanospheres and long circulating ('stealth') liposomes, substantially modulate the pharmacokinetics of existing compounds, and may also be useful to enhance the delivery of antifungal agents to sites of infection. Further insights into the structure-activity relationship of the antifungal triazoles that target the biosynthesis of ergosterol in the fungal cell membrane have led to the development of highly potent broad spectrum agents, including posaconazole, ravuconazole and voriconazole. Similarly, a novel generation of cell-wall active semisynthetic echinocandin 1,3 beta-glucan inhibitors (caspofungin, FK463, and VER-002) has entered clinical development. These agents have potent and broad-spectrum activity against Candida spp, and potentially useful activity against Aspergillus spp. and Pneumocystis carinii. The ongoing convergence of the fields of molecular pathogenesis, antifungal pharmacology and vaccine development will afford the opportunity to develop novel targets to complement the existing antifungal armamentarium.
侵袭性真菌感染新治疗方法的研发包括为已批准和正在研究的化合物开发新的给药系统,以及将细胞膜、细胞壁和毒力因子作为假定的抗真菌靶点加以利用。由环糊精、螺旋形分子、纳米颗粒/纳米球和长循环(“隐形”)脂质体组成的新型给药系统,可显著调节现有化合物的药代动力学,也可能有助于增强抗真菌药物向感染部位的递送。对靶向真菌细胞膜中麦角固醇生物合成的抗真菌三唑类药物构效关系的进一步深入了解,促成了高效广谱药物的研发,包括泊沙康唑、拉夫康唑和伏立康唑。同样,新一代具有细胞壁活性的半合成棘白菌素1,3-β-葡聚糖抑制剂(卡泊芬净、FK463和VER-002)已进入临床开发阶段。这些药物对念珠菌属具有强大的广谱活性,对曲霉菌属和卡氏肺孢子虫可能也有有效活性。分子发病机制、抗真菌药理学和疫苗开发领域的不断融合,将为开发新靶点提供机会,以补充现有的抗真菌药物库。