Antifungal activity against Scedosporium species and novel assays to assess antifungal pharmacodynamics against filamentous fungi

被引:28
|
作者
Wiederhold, Nathan P. [1 ,2 ]
Lewis, Russell E. [3 ,4 ]
机构
[1] UTHSCSA, PERC MSC 6220, San Antonio, TX 78229 USA
[2] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA
[3] Univ Houston, Coll Pharm, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
Scedosporium apiospermum; Scedosporium prolificans; XTT; DiBAC; antifungal pharmacology; IN-VITRO ACTIVITIES; LIPOSOMAL AMPHOTERICIN-B; ASPERGILLUS-FUMIGATUS; PSEUDALLESCHERIA-BOYDII; POLYMORPHONUCLEAR LEUKOCYTES; SYNERGISTIC INTERACTION; TRANSPLANT RECIPIENT; CANDIDA-ALBICANS; RADICAL SURGERY; GLUCAN SYNTHASE;
D O I
10.1080/13693780802510224
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The saprophytic moulds Scedosporium prolificans and Scedosporium apiospermum/Pseudallescheria boydii are an increasing cause of invasive fungal infections in immunocompromised hosts. The growing importance and high mortality rates of invasive disease caused by these fungi necessitates the search for newer treatment strategies. However, clinically available antifungal agents have modest to minimal activity against these organisms that has been confirmed by suboptimal responses in the clinic. Due to this limited in vitro activity and poor clinical response, antifungal combinations and high-dose regimens are frequently recommended to treat these refractory infections. However, development of a pharmacodynamic basis for antifungal dosing in scedosporiosis has been hampered by the limitations in the application of traditional microbiological techniques and endpoints for Scedosporium species. Newer quantitative and qualitative assays have demonstrated utility for measuring drug lethality in filamentous fungi, including Scedosporium species, and may aid in the development of new treatment strategies to improve patient outcomes.
引用
收藏
页码:422 / 432
页数:11
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