Imai Jackie, Singh Gaurav, Fernandez Belkys, Clemons Karl V, Stevens David A
California Institute for Medical Research, San Jose, 95128, USA.
J Antimicrob Chemother. 2005 Jul;56(1):166-71. doi: 10.1093/jac/dki178. Epub 2005 May 25.
Currently, few options exist to treat central nervous system (CNS) aspergillosis, which is usually fatal. We tested the efficacy of Abelcet and caspofungin, alone and in combination for treatment of this disease.
Male CD-1 mice were immunosuppressed with 200 mg/kg cyclophosphamide 2 days prior to infection and every 5 days thereafter. In the first study, mice were infected intracerebrally with 2.1 x 10(6) conidia/mouse of Aspergillus fumigatus; 10 days of once daily therapy began one day later. Groups of 10 received 0.8, 4, or 8 mg/kg of Abelcet, intravenously (iv), or caspofungin, intraperitoneally, 0.8 mg/kg of conventional amphotericin B (AmB) iv, or no treatment. In a second study, mice were challenged with 6.4 x 10(6) conidia and given no treatment, 8 mg/kg of Abelcet or caspofungin, alone or in combination. On day 14, cfu were determined in survivors by plating of organ homogenates.
In the first study, mice given any regimen of Abelcet or caspofungin had a survival rate > or =80% whereas untreated had 90% mortality. All drug regimens prolonged survival (P < or = 0.0008) and reduced cfu (P < or = 0.0001-0.003) recovered from the brains and kidneys compared with untreated. Abelcet showed an apparent dose-related reduction of cfu in the brains. Abelcet at 4 or 8 mg/kg were equivalent to AmB in reducing cfu from both organs (P > 0.05); AmB was superior to 0.8 mg/kg of Abelcet in the brain only (P < 0.02). Abelcet at 8 mg/kg or AmB at 0.8 mg/kg were superior to all regimens of caspofungin in reducing cfu (P < or = 0.05-0.001). In the second study, Abelcet alone significantly prolonged survival and reduced cfu in the organs versus the controls. Caspofungin did not significantly prolong survival or reduce cfu in comparison with the controls. In combination, Abelcet and caspofungin were equivalent to Abelcet alone.
Abelcet proved to be efficacious, but not curative, in the treatment of CNS aspergillosis and was equivalent overall to conventional AmB. Caspofungin was not as effective against the larger inoculum, but did not enhance or interfere with the efficacy of Abelcet. Since Abelcet displayed dose-responsive efficacy, it is possible higher doses could produce superior results, yet not show toxicity.
目前,治疗通常致命的中枢神经系统(CNS)曲霉病的方法很少。我们测试了两性霉素B脂质体(Abelcet)和卡泊芬净单独及联合治疗该疾病的疗效。
雄性CD-1小鼠在感染前2天用200mg/kg环磷酰胺进行免疫抑制,此后每5天一次。在第一项研究中,小鼠脑内接种2.1×10⁶个烟曲霉菌分生孢子/只;1天后开始为期10天的每日一次治疗。每组10只小鼠静脉注射(iv)0.8、4或8mg/kg的Abelcet,或腹腔注射0.8mg/kg的卡泊芬净,静脉注射0.8mg/kg的传统两性霉素B(AmB),或不治疗。在第二项研究中,小鼠接种6.4×10⁶个分生孢子,不治疗,单独或联合给予8mg/kg的Abelcet或卡泊芬净。在第14天,通过接种器官匀浆来确定存活小鼠的菌落形成单位(cfu)。
在第一项研究中,接受任何Abelcet或卡泊芬净治疗方案的小鼠存活率≥80%,而未治疗的小鼠死亡率为90%。与未治疗组相比,所有药物治疗方案均延长了生存期(P≤0.0008)并减少了从脑和肾中回收的cfu(P≤0.0001 - 0.003)。Abelcet在脑中显示出明显的与剂量相关的cfu减少。4或8mg/kg的Abelcet在减少两个器官的cfu方面与AmB相当(P>0.05);AmB仅在脑中优于0.8mg/kg的Abelcet(P<0.02)。8mg/kg的Abelcet或0.8mg/kg的AmB在减少cfu方面优于所有卡泊芬净治疗方案(P≤0.05 - 0.001)。在第二项研究中,单独使用Abelcet与对照组相比显著延长了生存期并减少了器官中的cfu。与对照组相比,卡泊芬净未显著延长生存期或减少cfu。联合使用时,Abelcet和卡泊芬净与单独使用Abelcet等效。
Abelcet在治疗CNS曲霉病方面被证明是有效的,但不能治愈,总体上与传统的AmB等效。卡泊芬净对较大接种量的效果不佳,但不增强或干扰Abelcet的疗效。由于Abelcet显示出剂量反应性疗效,更高剂量可能会产生更好的结果,且未显示出毒性。