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有潜力的抗真菌药物:当前抗真菌药物研发进展综述

Aspiring Antifungals: Review of Current Antifungal Pipeline Developments.

作者信息

Gintjee Thomas J, Donnelley Monica A, Thompson George R

机构信息

Department of Inpatient Pharmacy, University of California - Davis, 2315 Stockton Blvd., Room 1310, Sacramento, CA 95817, USA.

College of Pharmacy, Touro University, 1310 Club Drive, Vallejo, CA 94592, USA.

出版信息

J Fungi (Basel). 2020 Feb 25;6(1):28. doi: 10.3390/jof6010028.

Abstract

Invasive fungal infections are associated with significant morbidity and mortality, and their management is restricted to a variety of agents from five established classes of antifungal medication. In practice, existing antifungal agents are often constrained by dose-limiting toxicities, drug interactions, and the routes of administration. An increasing prevalence of invasive fungal infections along with rising rates of resistance and the practical limitations of existing agents has created a demand for the development of new antifungals, particularly those with novel mechanisms of action. This article reviews antifungal agents currently in various stages of clinical development. New additions to existing antifungal classes will be discussed, including SUBA-itraconazole, a highly bioavailable azole, and amphotericin B cochleate, an oral amphotericin formulation, as well as rezafungin, a long-acting echinocandin capable of once-weekly administration. Additionally, novel first-in-class agents such as ibrexafungerp, an oral glucan synthase inhibitor with activity against various resistant fungal isolates, and olorofim, a pyrimidine synthesis inhibitor with a broad spectrum of activity and oral formulation, will be reviewed. Various other innovative antifungal agents and classes, including MGCD290, tetrazoles, and fosmanogepix, will also be examined.

摘要

侵袭性真菌感染与显著的发病率和死亡率相关,其治疗局限于来自五类已确立的抗真菌药物中的多种药物。在实际应用中,现有的抗真菌药物常常受到剂量限制性毒性、药物相互作用及给药途径的限制。侵袭性真菌感染的患病率不断上升,耐药率也日益增加,同时现有药物存在实际局限性,这催生了对新型抗真菌药物的需求,尤其是那些具有新作用机制的药物。本文综述了目前处于临床开发各阶段的抗真菌药物。将讨论现有抗真菌类别中的新成员,包括生物利用度高的唑类药物SUBA-伊曲康唑、口服两性霉素制剂两性霉素B耳蜗形脂质体,以及能够每周给药一次的长效棘白菌素类药物瑞扎芬净。此外,还将综述新型的一流药物,如对多种耐药真菌分离株具有活性的口服葡聚糖合酶抑制剂ibrexafungerp,以及具有广泛活性和口服剂型的嘧啶合成抑制剂奥洛罗芬。还将研究各种其他创新的抗真菌药物和类别,包括MGCD290、四氮唑类和福斯马诺吉匹克。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ecd/7151215/0cef08618494/jof-06-00028-g001.jpg

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