Katragkou Aspasia, McCarthy Matthew, Meletiadis Joseph, Hussain Kaiser, Moradi Patriss W, Strauss Gittel E, Myint Kyaw L, Zaw Myo H, Kovanda Laura L, Petraitiene Ruta, Roilides Emmanuel, Walsh Thomas J, Petraitis Vidmantas
Transplantation-Oncology Infectious Diseases Program, Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, New York, USA.
Clinical Microbiology Laboratory, Attikon University Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Med Mycol. 2017 Nov 1;55(8):859-868. doi: 10.1093/mmy/myx006.
Combination therapy may be an alternative therapeutic approach for difficult-to-treat Candida infections with the aim of increasing efficacy of antifungal therapy. Whether isavuconazole, an extended-spectrum triazole, possesses synergistic activity in combination therapy with echinocandins or polyenes for the treatment of invasive candidiasis has not been studied. We used Bliss independence drug interaction analysis and time-kill assays to examine the in vitro interactions of isavuconazole with amphotericin B or micafungin, an echinocandin, against strains of Candida albicans, Candida parapsilosis, Candida glabrata, Candida tropicalis, and Candida krusei. The Bliss independence-based drug interactions modeling showed that the combination of isavuconazole and micafungin resulted in synergistic interactions against C. albicans, C. parapsilosis, and C. krusei. The degree of synergy ranged from 1.8% to 16.7% (mean %ΔΕ value) with the highest synergy occurring against C. albicans (⊙SYN% = 8.8%-110%). Time-kill assays showed that the isavuconazole-micafungin combination demonstrated concentration-depended synergy against C. albicans and C. parapsilosis. The combined interaction by Bliss analysis between isavuconazole and amphotericin B was indifferent for C. albicans, C. parapsilosis, and C. tropicalis while for C. glabrata was antagonistic (-2% to -6%) and C. krusei synergistic (3.4% to 7%). The combination of isavuconazole-amphotericin B by time-kill assay was antagonistic against C. krusei and C. glabrata. Collectively, our findings demonstrate that combinations of isavuconazole and micafungin are synergistic against Candida spp., while those of isavuconazole and amphotericin B are indifferent in vitro.
联合治疗可能是治疗难治性念珠菌感染的一种替代治疗方法,目的是提高抗真菌治疗的疗效。广谱三唑类药物艾沙康唑在与棘白菌素或多烯类药物联合治疗侵袭性念珠菌病时是否具有协同活性尚未得到研究。我们使用布利斯独立药物相互作用分析和时间杀菌试验,来检测艾沙康唑与两性霉素B或棘白菌素米卡芬净对白色念珠菌、近平滑念珠菌、光滑念珠菌、热带念珠菌和克柔念珠菌菌株的体外相互作用。基于布利斯独立的药物相互作用模型显示,艾沙康唑和米卡芬净联合使用对白色念珠菌、近平滑念珠菌和克柔念珠菌产生协同相互作用。协同程度为1.8%至16.7%(平均%ΔΕ值),其中对白色念珠菌的协同作用最强(⊙SYN% = 8.8%-110%)。时间杀菌试验表明,艾沙康唑-米卡芬净联合用药对白色念珠菌和近平滑念珠菌表现出浓度依赖性协同作用。通过布利斯分析,艾沙康唑与两性霉素B之间的联合相互作用对白色念珠菌、近平滑念珠菌和热带念珠菌无明显影响,而对光滑念珠菌具有拮抗作用(-2%至-6%),对克柔念珠菌具有协同作用(3.4%至7%)。通过时间杀菌试验,艾沙康唑-两性霉素B联合用药对克柔念珠菌和光滑念珠菌具有拮抗作用。总的来说,我们的研究结果表明,艾沙康唑和米卡芬净联合使用对念珠菌属具有协同作用,而艾沙康唑和两性霉素B联合使用在体外无明显相互作用。