New Directions in Antifungal Therapy.

D. Stevens
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引用次数: 3

Abstract

Development of antifungal therapy continues to be lively, as we strive to approach the ideal therapy. The newest agents include lipid delivery systems for amphotericin B, which promise relief from some of that drug's side effects. The triazoles, itraconazole and fluconazole, have proven their value as non-toxic and orally effective therapy. Newer members of this class, e. g., SCH 56592 and voriconazole, appear to be promising extensions. To date the triazoles' properties enable new strategies of prophylaxis and of early intervention. Areas needing improvement include treatment for newer fungal pathogens not covered by available therapy, and the need for rapid diagnostic capabilities, comparative clinical trials, and better definitions and scoring in trials. Drugs with new and fungal-specific targets may provide a quantum leap in our weaponry. Examples included drugs targeted at chitin synthase (e. g., nikkomycin Z) or beta glucan synthase (e. g., LY303366). Another approach is immunomodulation, and several cytokines can stimulate the host synergistically with conventional antifungal therapy.
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抗真菌治疗的新方向
抗真菌治疗的发展继续活跃,因为我们努力接近理想的治疗方法。最新的药物包括两性霉素B的脂质输送系统,它有望减轻药物的一些副作用。伊曲康唑和氟康唑等三唑类药物已被证明具有无毒和口服有效的治疗价值。这类药物的新成员,如SCH 56592和伏立康唑,似乎是有希望的扩展。迄今为止,三唑类药物的特性使预防和早期干预的新策略成为可能。需要改进的领域包括对现有治疗方法未涵盖的较新的真菌病原体的治疗,以及对快速诊断能力、比较临床试验和更好的定义和试验评分的需求。具有新的和真菌特异性靶标的药物可能会为我们的武器提供一个巨大的飞跃。例子包括靶向几丁质合成酶(如尼克霉素Z)或β -葡聚糖合成酶(如LY303366)的药物。另一种方法是免疫调节,几种细胞因子可以与传统的抗真菌治疗协同刺激宿主。
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