Dipartimento di Scienze di Laboratorio e Infettivologiche, Fondazione Policlinico Universitario "A. Gemelli" IRCCS, Rome, Italy.
Istituto di Microbiologia, Università Cattolica del Sacro Cuore, Rome, Italy.
J Antimicrob Chemother. 2019 Mar 1;74(Suppl 2):ii27-ii37. doi: 10.1093/jac/dkz041.
Improved standards of care depend on the development of new laboratory diagnostic and imaging procedures and the development of new antifungal compounds. Immunochromatography technologies have led to the development of lateral flow devices for the diagnosis of cryptococcal meningitis and invasive aspergillosis (IA). Similar devices are being developed for the detection of histoplasmosis that meet the requirements for speed (∼15 min assay time) and ease of use for point-of-care diagnostics. The evolution of molecular tools for the detection of fungal pathogens has been slow but the introduction of new nucleic acid amplification techniques appears to be helpful, for example T2Candida. An Aspergillus proximity ligation assay has been developed for a rapid near-patient bedside diagnosis of IA. CT remains the cornerstone for radiological diagnosis of invasive pulmonary fungal infections. MRI of the lungs may be performed to avoid radiation exposure. MRI with T2-weighted turbo-spin-echo sequences exhibits sensitivity and specificity approaching that of CT for the diagnosis of invasive pulmonary aspergillosis. The final part of this review looks at new approaches to drug discovery that have yielded new classes with novel mechanisms of action. There are currently two new classes of antifungal drugs in Phase 2 study for systemic invasive fungal disease and one in Phase 1. These new antifungal drugs show promise in meeting unmet needs with oral and intravenous formulations available and some with decreased potential for drug-drug interactions. Novel mechanisms of action mean these agents are not susceptible to the common resistance mechanisms seen in Candida or Aspergillus. Modification of existing antifungal susceptibility testing techniques may be required to incorporate these new compounds.
提高护理标准依赖于新的实验室诊断和成像程序的发展以及新的抗真菌化合物的开发。免疫层析技术已导致用于诊断隐球菌性脑膜炎和侵袭性曲霉病 (IA) 的侧向流动装置的发展。类似的设备正在为检测组织胞浆菌而开发,这些设备符合速度(约 15 分钟的检测时间)和即时护理诊断的易用性的要求。用于检测真菌病原体的分子工具的发展一直很缓慢,但新的核酸扩增技术的引入似乎有所帮助,例如 T2Candida。已经开发了一种曲霉属接近连接测定法,用于快速床边诊断侵袭性曲霉菌病。CT 仍然是侵袭性肺部真菌感染放射学诊断的基石。可以进行肺部 MRI 以避免辐射暴露。T2 加权涡轮自旋回波序列的 MRI 对诊断侵袭性肺曲霉病具有接近 CT 的敏感性和特异性。本综述的最后一部分着眼于药物发现的新方法,这些方法产生了具有新型作用机制的新型药物类别。目前有两种新的抗真菌药物处于系统性侵袭性真菌感染的 2 期研究阶段,有一种处于 1 期研究阶段。这些新的抗真菌药物有希望通过提供口服和静脉制剂并减少一些药物相互作用的潜力来满足未满足的需求。新型作用机制意味着这些药物不易受到常见的念珠菌或曲霉属的耐药机制的影响。可能需要修改现有的抗真菌药敏试验技术来纳入这些新化合物。