Seyedmousavi S, Chang Y C, Youn J H, Law D, Birch M, Rex J H, Kwon-Chung K J
Microbiology Service, Department of Laboratory Medicine, Clinical Center, National Institutes of Health, Bethesda, Maryland, USA.
Molecular Microbiology Section, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Antimicrob Agents Chemother. 2021 Sep 17;65(10):e0043421. doi: 10.1128/AAC.00434-21. Epub 2021 Jul 12.
Clinically relevant members of the / species complex and Lomentospora prolificans are generally resistant against currently available systemic antifungal agents , and infection due to these species is difficult to treat. We studied the efficacy of a new fungicidal agent, olorofim (formerly F901318), against scedosporiosis and lomentosporiosis in neutropenic animals. Cyclophosphamide-immunosuppressed CD-1 mice infected by Scedosporium apiospermum, Pseudallescheria boydii (Scedosporium boydii), and Lomentospora prolificans were treated by intraperitoneal administration of olorofim (15 mg/kg of body weight every 8 h for 9 days). The efficacy of olorofim treatment was assessed by the survival rate at 10 days postinfection, levels of serum (1-3)-β-d-glucan (BG), histopathology, and fungal burdens of kidneys 3 days postinfection. Olorofim therapy significantly improved survival compared to that of the untreated controls; 80%, 100%, and 100% of treated mice survived infection by Scedosporium apiospermum, Pseudallescheria boydii, and Lomentospora prolificans, respectively, while less than 20% of the control mice (phosphate-buffered saline [PBS] treated) survived at 10 days postinfection. In the olorofim-treated neutropenic CD-1 mice infected with any of the three species, serum BG levels were significantly suppressed and fungal DNA detected in the target organs was significantly lower than in controls. Furthermore, histopathology of kidneys revealed no or only a few lesions with hyphal elements in the olorofim-treated mice, while numerous fungal hyphae were present in control mice. These results indicate olorofim to be a promising therapeutic agent for systemic scedosporiosis/lomentosporiosis, devastating emerging fungal infections that are difficult to treat with currently available antifungals.
该菌/物种复合体以及多育镰孢菌中具有临床相关性的成员通常对目前可用的全身性抗真菌药物具有抗性,并且由这些菌种引起的感染难以治疗。我们研究了一种新型杀真菌剂奥洛菲姆(原名F901318)对中性粒细胞减少动物的赛多孢子菌病和多育镰孢菌病的疗效。用环磷酰胺免疫抑制的CD-1小鼠感染了尖端赛多孢子菌、波氏假阿利什菌(博伊德赛多孢子菌)和多育镰孢菌,通过腹腔注射奥洛菲姆(每8小时15毫克/千克体重,共9天)进行治疗。通过感染后10天的存活率、血清(1-3)-β-d-葡聚糖(BG)水平、组织病理学以及感染后3天肾脏中的真菌负荷来评估奥洛菲姆治疗的疗效。与未治疗的对照组相比,奥洛菲姆治疗显著提高了存活率;感染尖端赛多孢子菌、波氏假阿利什菌和多育镰孢菌的治疗小鼠分别有80%、100%和100%存活,而在感染后10天,对照组小鼠(用磷酸盐缓冲盐水[PBS]处理)存活的不到20%。在感染这三种菌种中任何一种的经奥洛菲姆治疗的中性粒细胞减少CD-1小鼠中,血清BG水平显著降低,并且在靶器官中检测到的真菌DNA明显低于对照组。此外,肾脏组织病理学显示,经奥洛菲姆治疗的小鼠没有或只有少数带有菌丝成分的病变,而对照小鼠中有大量真菌菌丝。这些结果表明,奥洛菲姆是治疗全身性赛多孢子菌病/多育镰孢菌病的一种有前景的治疗药物,全身性赛多孢子菌病/多育镰孢菌病是目前可用抗真菌药物难以治疗的毁灭性新发真菌感染。