Lestner Jodi, McEntee Laura, Johnson Adam, Livermore Joanne, Whalley Sarah, Schwartz Julie, Perfect John R, Harrison Thomas, Hope William
Antimicrobial Pharmacodynamics and Therapeutics, Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, United Kingdom
Antimicrobial Pharmacodynamics and Therapeutics, Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, United Kingdom.
Antimicrob Agents Chemother. 2017 May 24;61(6). doi: 10.1128/AAC.00090-17. Print 2017 Jun.
Cryptococcal meningoencephalitis is a rapidly lethal infection in immunocompromised patients. Induction regimens are usually administered for 2 weeks. The shortest effective period of induction therapy with liposomal amphotericin B (LAMB) is unknown. The pharmacodynamics of LAMB were studied in murine and rabbit models of cryptococcal meningoencephalitis. The concentrations of LAMB in the plasma and brains of mice were measured using high-performance liquid chromatography (HPLC). Histopathological changes were determined. The penetration of LAMB into the brain was determined by immunohistochemistry using an antibody directed to amphotericin B. A dose-dependent decline in fungal burden was observed in the brains of mice, with near-maximal efficacy achieved with LAMB at 10 to 20 mg/kg/day. The terminal elimination half-life in the brain was 133 h. The pharmacodynamics of a single dose of 20 mg/kg was the same as that of 20 mg/kg/day administered for 2 weeks. Changes in quantitative counts were reflected by histopathological changes in the brain. Three doses of LAMB at 5 mg/kg/day in rabbits were required to achieve fungicidal activity in cerebrospinal fluid (cumulative area under the concentration-time curve, 2,500 mg · h/liter). Amphotericin B was visible in the intra- and perivascular spaces, the leptomeninges, and the choroid plexus. The prolonged mean residence time of amphotericin B in the brain suggests that abbreviated induction regimens of LAMB are possible for cryptococcal meningoencephalitis.
隐球菌性脑膜脑炎在免疫功能低下患者中是一种迅速致命的感染。诱导治疗方案通常持续2周。脂质体两性霉素B(LAMB)诱导治疗的最短有效时间尚不清楚。在隐球菌性脑膜脑炎的小鼠和兔模型中研究了LAMB的药效学。使用高效液相色谱法(HPLC)测量小鼠血浆和脑中LAMB的浓度。确定组织病理学变化。使用抗两性霉素B抗体通过免疫组织化学确定LAMB在脑中的渗透情况。在小鼠脑中观察到真菌负荷呈剂量依赖性下降,LAMB以10至20mg/kg/天给药时达到近乎最大疗效。脑中的终末消除半衰期为133小时。单剂量20mg/kg的药效学与2周内每天给药20mg/kg相同。定量计数的变化通过脑内的组织病理学变化反映出来。在兔中,每天5mg/kg的LAMB需要三剂才能在脑脊液中达到杀菌活性(浓度-时间曲线下的累积面积,2500mg·h/升)。在血管内和血管周围间隙、软脑膜和脉络丛中可见两性霉素B。两性霉素B在脑中延长的平均驻留时间表明,对于隐球菌性脑膜脑炎,LAMB的简化诱导治疗方案是可行的。