Treviño-Rangel Rogelio de J, González Gloria M, Montoya Alexandra M, Rojas Olga C, Elizondo-Zertuche Mariana, Álvarez-Villalobos Neri A
Departamento de Microbiología, Facultad de Medicina, Universidad Autónoma de Nuevo León-Francisco I. Madero & Dr. Eduardo A. Pequeño, Mitras Centro, Monterrey 64460, Mexico.
Plataforma INVEST Medicina UANL-KER Unit Mayo Clinic (KER Unit Mexico), Facultad de Medicina, Universidad Autónoma de Nuevo León-Francisco I. Madero, Mitras Centro, Monterrey 64460, Mexico.
J Fungi (Basel). 2022 Oct 28;8(11):1144. doi: 10.3390/jof8111144.
The alarming spread and impact of multidrug-resistant 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 . 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 MIC: 0.03 mg/L), followed by ibrexafungerp (overall MIC: 1 mg/L) and rezafungin (overall MIC mode: 0.25 mg/L), while VT-1598 and ATI-2307 were the least explored drugs against . All these compounds demonstrated significant improvements in survival and reduction in tissue fungal burden on neutropenic animal models of candidemia due to . Continual efforts towards the discovery of new treatments against this multidrug-resistant fungus are essential.
多重耐药感染的惊人传播和影响,以及有限的治疗选择,促使了新型抗真菌药物的研发。这些有前景的药物目前正处于不同的研发阶段,提供了新的给药方案和作用机制。截至2022年6月27日,在MEDLINE、EMBASE、科学网和Scopus中进行了系统检索,以查找相关文章,报告研究性抗真菌药物对……的体外活性和体内疗效数据。这些药物包括现有抗真菌类别中的新成员(瑞扎芬净和奥泊康唑)、一类新药,如ibrexafungerp、甘露糖聚醚/磷甘露糖聚醚、奥洛罗芬和四氮唑类(喹赛康唑、奥替康唑和VT-1598),以及其他创新药物,如ATI-2307、MGCD290和VL-2397。在初步检索中检索到的592篇文章中,27篇符合纳入标准。研究最多的药物是甘露糖聚醚/磷甘露糖聚醚(总体MIC:0.03 mg/L),其次是ibrexafungerp(总体MIC:1 mg/L)和瑞扎芬净(总体MIC模式:0.25 mg/L),而VT-1598和ATI-2307是针对……研究最少的药物。所有这些化合物在因……导致的念珠菌血症中性粒细胞减少动物模型中,均显示出存活率显著提高,组织真菌负荷降低。持续努力发现针对这种多重耐药真菌的新治疗方法至关重要。