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体内三唑类药物和棘白菌素联合治疗侵袭性肺曲霉病:增强对 Cyp51 突变株的疗效。

Impact of in vivo triazole and echinocandin combination therapy for invasive pulmonary aspergillosis: enhanced efficacy against Cyp51 mutant isolates.

机构信息

University of Wisconsin, Madison, Wisconsin, USA.

出版信息

Antimicrob Agents Chemother. 2013 Nov;57(11):5438-47. doi: 10.1128/AAC.00833-13. Epub 2013 Aug 19.

Abstract

Previous studies examining combination therapy for invasive pulmonary aspergillosis (IPA) have revealed conflicting results, including antagonism, indifference, and enhanced effects. The most commonly employed combination for this infection includes a mold-active triazole and echinocandin. Few studies have evaluated combination therapy from a pharmacodynamic (PD) perspective, and even fewer have examined combination therapy against both wild-type and azole-resistant Cyp51 mutant isolates. The current studies aim to fill this gap in knowledge. Four Aspergillus fumigatus isolates were utilized, including a wild-type strain, an Fks1 mutant (posaconazole susceptible and caspofungin resistant), and two Cyp51 mutants (posaconazole resistant). A neutropenic murine model of IPA was used for the treatment studies. The dosing design included monotherapy with posaconazole, monotherapy with caspofungin, and combination therapy with both. Efficacy was determined using quantitative PCR, and results were normalized to known quantities of conidia (conidial equivalents [CE]). The static dose, 1-log kill dose, and associated PD target area under the curve (AUC)/MIC ratio were determined for monotherapy and combination therapy. Monotherapy experiments revealed potent activity for posaconazole, with reductions of 3 to 4 log10 Aspergillus CE/ml with the two "low"-MIC isolates. Posaconazole alone was less effective for the two isolates with higher MICs. Caspofungin monotherapy did not produce a significant decrease in fungal burden for any strain. Combination therapy with the two antifungals did not enhance efficacy for the two posaconazole-susceptible isolates. However, the drug combination produced synergistic activity against both posaconazole-resistant isolates. Specifically, the combination resulted in a 1- to 2-log10 decline in burden that would not have been predicted based on the monotherapy results for each drug. This corresponded to a reduction in the free-drug posaconazole AUC/MIC ratio needed for stasis of up to 17-fold. The data suggest that combination therapy using a triazole and an echinocandin may be a beneficial treatment strategy for triazole-resistant isolates.

摘要

先前研究侵袭性肺曲霉病(IPA)联合治疗的结果相互矛盾,包括拮抗、无影响和增强作用。这种感染最常用的联合治疗包括一种有活性的三唑和棘白菌素。很少有研究从药效学(PD)角度评估联合治疗,更少研究针对野生型和唑类耐药 Cyp51 突变株的联合治疗。目前的研究旨在填补这一知识空白。研究使用了 4 株烟曲霉分离株,包括野生型菌株、Fks1 突变株(泊沙康唑敏感和卡泊芬净耐药)和 2 株 Cyp51 突变株(泊沙康唑耐药)。使用中性粒细胞减少的 IPA 啮齿动物模型进行治疗研究。给药设计包括泊沙康唑单药治疗、卡泊芬净单药治疗和联合治疗。采用定量 PCR 测定疗效,并将结果归一化为已知数量的分生孢子(分生孢子当量[CE])。确定了单药和联合治疗的静态剂量、1 对数杀灭剂量和相关 PD 目标 AUC/MIC 比值。单药实验显示泊沙康唑具有强大的活性,两种“低”MIC 分离株的减少量为 3 至 4 log10 Aspergillus CE/ml。对于 MIC 较高的两种分离株,泊沙康唑单药治疗效果较差。卡泊芬净单药治疗对任何菌株的真菌负荷均未显著降低。两种抗真菌药物的联合治疗对两种泊沙康唑敏感的分离株没有增强疗效。然而,该药物联合对两种泊沙康唑耐药的分离株产生了协同作用。具体而言,联合治疗导致负荷下降 1 至 2 log10,这与每种药物的单药治疗结果不符。这相当于使唑类药物泊沙康唑的游离药物 AUC/MIC 比值稳定所需的减少高达 17 倍。数据表明,使用三唑和棘白菌素的联合治疗可能是治疗唑类耐药分离株的有益治疗策略。

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