Antifungal resistance: current trends and future strategies to combat

被引:316
作者
Wiederhold, Nathan P. [1 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Pathol & Lab Med, Fungus Testing Lab, San Antonio, TX 78229 USA
关键词
azoles; echinocandins; Aspergillus; Candida albicans; investigational antifungals; non-albicans Candida species; acquired resistance; intrinsic resistance; Candida auris; IN-VITRO ACTIVITY; BROAD-SPECTRUM ANTIFUNGAL; INFECTIOUS-DISEASES SOCIETY; GLUCAN SYNTHASE INHIBITOR; CLSI BROTH MICRODILUTION; BLOOD-STREAM INFECTIONS; HIGHLY POTENT INHIBITOR; ASPERGILLUS-FUMIGATUS; INVASIVE CANDIDIASIS; AZOLE RESISTANCE;
D O I
10.2147/IDR.S124918
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Antifungal resistance represents a major clinical challenge to clinicians responsible for treating invasive fungal infections due to the limited arsenal of systemically available antifungal agents. In addition current drugs may be limited by drug-drug interactions and serious adverse effects/toxicities that prevent their prolonged use or dosage escalation. Fluconazole resistance is of particular concern in non-Candida albicans species due to the increased incidence of infections caused by these species in different geographic locations worldwide and the elevated prevalence of resistance to this commonly used azole in many institutions. C. glabrata resistance to the echinocandins has also been documented to be rising in several US institutions, and a higher percentage of these isolates may also be azole resistant. Azole resistance in Aspergillus fumigatus due to clinical and environmental exposure to this class of agents has also been found worldwide, and these isolates can cause invasive infections with high mortality rates. In addition, several species of Aspergillus, and other molds, including Scedosporium and Fusarium species, have reduced susceptibility or pan-resistance to clinically available antifungals. Various investigational antifungals are currently in preclinical or clinical development, including several of them that have the potential to overcome resistance observed against the azoles and the echinocandins. These include agents that also target ergosterol and beta-glucan biosynthesis, as well as compounds with novel mechanisms of action that may also overcome the limitations of currently available antifungal classes, including both resistance and adverse effects/ toxicity.
引用
收藏
页码:249 / 259
页数:11
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