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新型抗真菌药物的药效学、作用机制与耐药性以及活性谱

Pharmacodynamics, Mechanisms of Action and Resistance, and Spectrum of Activity of New Antifungal Agents.

作者信息

Wiederhold Nathan P

机构信息

Fungus Testing Laboratory, Department of Pathology and Laboratory Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.

出版信息

J Fungi (Basel). 2022 Aug 16;8(8):857. doi: 10.3390/jof8080857.

Abstract

Several new antifungals are currently in late-stage development, including those with novel pharmacodynamics/mechanisms of action that represent new antifungal classes (manogepix, olorofim, ATI-2307, GR-2397). Others include new agents within established classes or with mechanisms of action similar to clinically available antifungals (ibrexafungerp, rezafungin, oteseconazole, opelconazole, MAT2203) that have been modified in order to improve certain characteristics, including enhanced pharmacokinetics and greater specificity for fungal targets. Many of the antifungals under development also have activity against and strains that have reduced susceptibility or acquired resistance to azoles and echinocandins, whereas others demonstrate activity against species that are intrinsically resistant to most clinically available antifungals. The tolerability and drug-drug interaction profiles of these new agents also appear to be promising, although the number of human subjects that have been exposed to many of these agents remains relatively small. Overall, these agents have the potential for expanding our antifungal armamentarium and improving clinical outcomes in patients with invasive mycoses.

摘要

目前有几种新型抗真菌药物正处于后期研发阶段,其中包括具有新型药效学/作用机制、代表新抗真菌类别的药物(曼诺地昔、奥拉罗芬、ATI-2307、GR-2397)。其他还包括现有类别中的新药物,或作用机制与临床可用抗真菌药物相似的药物(依布列夏芬净、瑞扎芬净、奥替康唑、奥佩康唑、MAT2203),这些药物经过改良以改善某些特性,包括增强药代动力学和对真菌靶点更高的特异性。许多正在研发的抗真菌药物还对唑类和棘白菌素敏感性降低或获得性耐药的 和 菌株具有活性,而其他药物则对大多数临床可用抗真菌药物固有耐药的菌种具有活性。这些新药的耐受性和药物相互作用情况似乎也很有前景,尽管接触过其中许多药物的人类受试者数量仍然相对较少。总体而言,这些药物有可能扩充我们的抗真菌药物库,并改善侵袭性真菌病患者的临床结局。

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