Division of Dermatology, National Skin Centre, Singapore City, Singapore.
Australas J Dermatol. 2023 Aug;64(3):315-321. doi: 10.1111/ajd.14115. Epub 2023 Jun 30.
The incidence and prevalence of recalcitrant cutaneous fungal infections is on the rise. Terbinafine-resistant Trichophyton has not only been widespread in India, but has also been reported in countries spread throughout the globe. Strains of yeasts such as Malassezia and Candida, which exist both as commensals and as pathogens to the human skin, have also been found to develop resistance to antifungals. Non-dermatophyte moulds which can colonize and infect damaged nails are especially difficult to treat, not only due to resistance, but also because of poor drug penetration of hard keratin. Psychosocial factors such as the indiscriminate broad-spectrum antifungal use in agriculture and in medicine, and poor adherence to hygienic measures to break the chain of infection contribute to the development of antifungal resistance. Such environments encourage fungi to develop various resistance mechanisms to withstand antifungal treatment. These include: (a) alteration of the drug target, (b) increasing efflux of drug/metabolites, (c) inactivation of drug, (d) bypass mechanisms or substitution of the pathway affected by the drug, (e) stress adaptation mechanisms and (f) biofilm formation. Understanding of such mechanisms and how they arise are crucial for development of new ways to prevent or overcome resistance. Novel antifungal treatments have recently been approved in the United States of America for treatment of vulvovaginal candidiasis. Ibrexafungerp (enfumafungin derivative) and oteseconazole (tetrazole) differ from their respective related drug classes of echinocandins and triazoles by having different structures, which lend these medicines advantage compared to traditional treatment by having a different binding site and more selectivity for fungi respectively. Other drugs designed to circumvent the known mechanisms of antifungal resistance are also at various phases of development. Concurrent measures at an institutional and individual level to address and limit inappropriate antifungal use to reduce development of antifungal resistance should be undertaken in a concerted effort to address this epidemic.
顽固性皮肤真菌感染的发病率和患病率呈上升趋势。特比萘芬耐药的毛癣菌不仅在印度广泛存在,而且在全球范围内的许多国家也有报道。马拉色菌和念珠菌等酵母菌,它们既是人类皮肤的共生菌,也是病原体,也被发现对抗真菌药物产生了耐药性。能够定植和感染受损指甲的非皮肤真菌,尤其难以治疗,不仅因为耐药性,还因为硬角蛋白的药物渗透不良。社会心理因素,如农业和医学中广谱抗真菌药物的滥用以及对打破感染链的卫生措施的依从性差,都有助于抗真菌药物耐药性的发展。这些环境促使真菌发展出各种耐药机制来抵御抗真菌治疗。这些机制包括:(a) 药物靶标改变,(b) 增加药物/代谢物的外排,(c) 药物失活,(d) 绕过药物作用途径的替代机制或替代途径,(e) 应激适应机制和 (f) 生物膜形成。了解这些机制以及它们是如何产生的,对于开发预防或克服耐药性的新方法至关重要。最近在美国批准了新的抗真菌药物治疗外阴阴道念珠菌病。Ibrexafungerp(恩氟米康唑衍生物)和 oteseconazole(四唑)与各自相关的棘白菌素和三唑类药物不同,其结构不同,与传统治疗相比,这些药物具有不同的结合位点和对真菌的更高选择性,因此具有优势。其他旨在规避已知抗真菌耐药机制的药物也处于不同的开发阶段。在机构和个人层面上采取同步措施来解决和限制不适当的抗真菌药物使用,以减少抗真菌药物耐药性的发展,应该协同努力来解决这一流行问题。