Petraitis Vidmantas, Petraitiene Ruta, Groll Andreas H, Roussillon Kristin, Hemmings Melissa, Lyman Caron A, Sein Tin, Bacher John, Bekersky Ihor, Walsh Thomas J
Immunocompromised Host Section, Pediatric Oncology Branch, National Cancer Institute, Bethesda, Maryland 20892, USA.
Antimicrob Agents Chemother. 2002 Jun;46(6):1857-69. doi: 10.1128/AAC.46.6.1857-1869.2002.
Micafungin (FK463) is an echinocandin that demonstrates potent in vitro antifungal activities against Candida and Aspergillus species. However, little is known about its comparative antifungal activities in persistently neutropenic hosts. We therefore investigated the plasma micafungin pharmacokinetics and antifungal activities of micafungin against experimental disseminated candidiasis and invasive pulmonary aspergillosis in persistently neutropenic rabbits. The groups with disseminated candidiasis studied consisted of untreated controls (UCs); rabbits treated with desoxycholate amphotericin B (DAMB) at 1 mg/kg of body weight/day; or rabbits treated with micafungin at 0.25, 0.5, 1, and 2 mg/kg/day intravenously. Compared with the UCs, rabbits treated with micafungin or DAMB showed significant dosage-dependent clearance of Candida albicans from the liver, spleen, kidney, brain, eye, lung, and vena cava. These in vivo findings correlated with the results of in vitro time-kill assays that demonstrated that micafungin has concentration-dependent fungicidal activity. The groups with invasive pulmonary aspergillosis studied consisted of UCs; rabbits treated with DAMB; rabbits treated with liposomal amphotericin B (LAMB) at 5 mg/kg/day; and rabbits treated with micafungin at 0.5, 1, and 2 mg/kg/day. In comparison to the significant micafungin dosage-dependent reduction of the residual burden (in log CFU per gram) of C. albicans in tissue, micafungin-treated rabbits with invasive pulmonary aspergillosis had no reduction in the concentration of Aspergillus fumigatus in tissue. DAMB and LAMB significantly reduced the burdens of C. albicans and A. fumigatus in tissues (P < 0.01). Persistent galactomannan antigenemia in micafungin-treated rabbits correlated with the presence of an elevated burden of A. fumigatus in pulmonary tissue. By comparison, DAMB- and LAMB-treated animals had significantly reduced circulating galactomannan antigen levels. Despite a lack of clearance of A. fumigatus from the lungs, there was a significant improvement in the rate of survival (P < 0.001) and a reduction in the level of pulmonary infarction (P < 0.05) in micafungin-treated rabbits. In summary, micafungin demonstrated concentration-dependent and dosage-dependent clearance of C. albicans from persistently neutropenic rabbits with disseminated candidiasis but not of A. fumigatus from persistently neutropenic rabbits with invasive pulmonary aspergillosis.
米卡芬净(FK463)是一种棘白菌素,在体外对念珠菌属和曲霉属具有强大的抗真菌活性。然而,对于其在持续性中性粒细胞减少宿主中的比较抗真菌活性知之甚少。因此,我们研究了米卡芬净在持续性中性粒细胞减少兔体内的血浆药代动力学以及其对实验性播散性念珠菌病和侵袭性肺曲霉病的抗真菌活性。研究的播散性念珠菌病组包括未治疗的对照组(UCs);接受脱氧胆酸盐两性霉素B(DAMB)治疗,剂量为1mg/kg体重/天的兔;或接受米卡芬净治疗,剂量分别为0.25、0.5、1和2mg/kg/天静脉注射的兔。与UCs相比,接受米卡芬净或DAMB治疗的兔肝脏、脾脏、肾脏、大脑、眼睛、肺和腔静脉中的白色念珠菌有显著的剂量依赖性清除。这些体内研究结果与体外时间杀菌试验结果相关,该试验表明米卡芬净具有浓度依赖性杀菌活性。研究的侵袭性肺曲霉病组包括UCs;接受DAMB治疗的兔;接受脂质体两性霉素B(LAMB)治疗,剂量为5mg/kg/天的兔;以及接受米卡芬净治疗,剂量分别为0.5、1和2mg/kg/天的兔。与米卡芬净剂量依赖性显著降低组织中白色念珠菌的残留负荷(每克组织中的对数CFU)相比,接受米卡芬净治疗的侵袭性肺曲霉病兔组织中烟曲霉的浓度没有降低。DAMB和LAMB显著降低了组织中白色念珠菌和烟曲霉的负荷(P<0.01)。米卡芬净治疗的兔持续半乳甘露聚糖抗原血症与肺组织中烟曲霉负荷升高有关。相比之下,接受DAMB和LAMB治疗的动物循环半乳甘露聚糖抗原水平显著降低。尽管米卡芬净未能清除肺部的烟曲霉,但接受米卡芬净治疗的兔的生存率有显著提高(P<0.001),肺梗死水平降低(P<0.05)。总之,米卡芬净在持续性中性粒细胞减少的播散性念珠菌病兔中对白色念珠菌具有浓度依赖性和剂量依赖性清除作用,但在持续性中性粒细胞减少的侵袭性肺曲霉病兔中对烟曲霉没有这种作用。