耳念珠菌抗真菌管道研究进展:系统综述。

Rogelio de J Treviño-Rangel, Gloria M González, Alexandra M Montoya, Olga C Rojas, Mariana Elizondo-Zertuche, Neri A Álvarez-Villalobos
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引用次数: 9

摘要

多重耐药耳念珠菌感染的惊人传播和影响以及有限的治疗选择促使开发新的抗真菌药物。这些有前景的药物目前处于不同的开发阶段,提供了新的给药方案和作用机制。系统检索截至2022年6月27日的MEDLINE、EMBASE、Web of Science和Scopus数据库,查找研究中抗真菌药物抗C. auris体外活性和体内疗效的相关文章。这些药物包括现有抗真菌类药物(rezafungin和opelconazole)的新添加药物,ibrexafungerp、manogepix/ fosmangepix、olorofim和tetrazoles (quilseconazole、oteseconazole和VT-1598)等同类药物,以及ATI-2307、MGCD290和VL-2397等其他创新药物。在主要检索中检索到的592篇文章中,有27篇符合资格标准。研究最多的药物是manogepix/ fosmangepix(总MIC90: 0.03 mg/L),其次是ibrexafungerp(总MIC90: 1 mg/L)和rezafungin(总MIC模式:0.25 mg/L),而研究最少的药物是tt -1598和ATI-2307。所有这些化合物在金黄色念珠菌引起的嗜中性粒细胞减少的动物模型上显示出显著的生存改善和减少组织真菌负担。必须不断努力发现针对这种多重耐药真菌的新疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Recent Antifungal Pipeline Developments against <i>Candida auris</i>: A Systematic Review.

Recent Antifungal Pipeline Developments against Candida auris: A Systematic Review.

The alarming spread and impact of multidrug-resistant Candida auris infections alongside the limited therapeutic options have prompted the development of new antifungals. These promising agents are currently in different stages of development, offering novel dosing regimens and mechanisms of action. A systematic search in MEDLINE, EMBASE, Web of Science, and Scopus up to 27 June 2022 was conducted to find relevant articles reporting data of in vitro activity and in vivo efficacy of investigational antifungals against C. auris. These included new additions to existing antifungal classes (rezafungin and opelconazole), first-in-class drugs such as ibrexafungerp, manogepix/fosmanogepix, olorofim and tetrazoles (quilseconazole, oteseconazole and VT-1598), as well as other innovative agents like ATI-2307, MGCD290 and VL-2397. From 592 articles retrieved in the primary search, 27 met the eligibility criteria. The most studied agent was manogepix/fosmanogepix (overall MIC90: 0.03 mg/L), followed by ibrexafungerp (overall MIC90: 1 mg/L) and rezafungin (overall MIC mode: 0.25 mg/L), while VT-1598 and ATI-2307 were the least explored drugs against C. auris. All these compounds demonstrated significant improvements in survival and reduction in tissue fungal burden on neutropenic animal models of candidemia due to C. auris. Continual efforts towards the discovery of new treatments against this multidrug-resistant fungus are essential.

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