Quindós Guillermo, Carrillo-Muñoz Alfonso Javier, Eraso Elena, Cantón Emilia, Pemán Javier
Laboratorio de Micología Médica, Departamento de Inmunología, Microbiología y Parasitología, Facultad de Medicina y Odontología, Universidad del País Vasco, Bilbao, Spain.
Rev Iberoam Micol. 2007 Sep 30;24(3):198-208. doi: 10.1016/s1130-1406(07)70043-8.
Voriconazole has been developed to meet the increasing need for new and useful antifungal agents for the treatment of invasive mycoses. This review describes the spectrum of voriconazole antifungal activity based on data from in vitro studies published during the last three years. This survey demonstrates that voriconazole has a broad antifungal spectrum against the most common fungal pathogens being its action fungistatic for Candida and fungicidal for Aspergillus and other filamentous fungi. Overall, more than 95% of all Candida isolates tested are susceptible to voriconazole and less than 3% are resistant. Similar or even better activity rates have been described for Aspergillus, Cryptococcus and most of yeasts and moulds of medical importance. We also discuss the limitations related to the azole cross-resistance observed in some Candida glabrata isolates, the poor activity of voriconazole against Scedosporium prolificans, its activity against fungal biofilms and the great potential usefulness of combination of voriconazole with other antifungal drugs.
伏立康唑的研发是为了满足治疗侵袭性真菌病对新型有效抗真菌药物日益增长的需求。本综述基于过去三年发表的体外研究数据,描述了伏立康唑的抗真菌活性谱。这项调查表明,伏立康唑对最常见的真菌病原体具有广泛的抗真菌谱,其对念珠菌的作用是抑菌,对曲霉菌和其他丝状真菌是杀菌。总体而言,超过95%的受试念珠菌分离株对伏立康唑敏感,不到3%耐药。对于曲霉菌、隐球菌以及大多数具有医学重要性的酵母菌和霉菌,也有类似甚至更好的活性率报道。我们还讨论了在一些光滑念珠菌分离株中观察到的与唑类交叉耐药相关的局限性、伏立康唑对多育赛多孢菌的活性较差、其对真菌生物膜的活性以及伏立康唑与其他抗真菌药物联合使用的巨大潜在用途。