Mehta R T
Department of Bioimmunotherapy, University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.
Antimicrob Agents Chemother. 1996 Aug;40(8):1893-902. doi: 10.1128/AAC.40.8.1893.
Disseminated infections caused by the Mycobacterium avium-M. intracellulare complex (MAC) are the most frequent opportunistic bacterial infections in patients with AIDS. MAC isolates are resistant to many of the standard antituberculous drugs. Failure to obtain significant activities of certain drugs is due to difficulty in achieving high concentrations at the sites where the infections reside. New and improved agents for the treatment of mycobacterial infections are therefore required. Earlier, the anti-MAC activities of various agents in free or liposomal form were studied; liposomes were used as drug carriers to ultimately target the drugs to macrophages where mycobacterial infections reside. Clofazimine was chosen for further studies because it could be effectively encapsulated and its activity was well maintained in liposomal form. The present studies with both erythrocytes and macrophages as the model systems show that liposomal drug is far less toxic in vitro than the free drug. The in vivo toxicity of clofazimine was also significantly reduced after liposome encapsulation. The therapeutic efficacies of free and liposomal drugs were compared in a beige mouse model of disseminated MAC infection. An equivalent dose of liposomal drug (10 mg/kg of body weight) was more effective in eliminating the bacterial from the various organs studied, particularly from the liver. Moreover, because of the reduced toxicity of liposomal drug, higher doses could be administered, resulting in a significant reduction in the numbers of CFU in the liver, spleen, and kidneys. The data demonstrate that liposomal clofazimine is highly effective in the treatment of MAC infections, even if the treatment is initiated after a disseminated infection has been established. The present studies thus suggest the potential usefulness of liposomal clofazimine for the treatment of disseminated MAC infections.
由鸟分枝杆菌-胞内分枝杆菌复合体(MAC)引起的播散性感染是艾滋病患者中最常见的机会性细菌感染。MAC分离株对许多标准抗结核药物耐药。某些药物未能获得显著活性是由于难以在感染部位达到高浓度。因此,需要新的和改进的治疗分枝杆菌感染的药物。早些时候,研究了各种游离或脂质体形式药物的抗MAC活性;脂质体被用作药物载体,最终将药物靶向到存在分枝杆菌感染的巨噬细胞。选择氯法齐明进行进一步研究,因为它可以有效地被包封,并且其活性以脂质体形式得到很好的维持。目前以红细胞和巨噬细胞作为模型系统的研究表明,脂质体药物在体外的毒性远低于游离药物。氯法齐明经脂质体包封后,其体内毒性也显著降低。在播散性MAC感染的米色小鼠模型中比较了游离药物和脂质体药物的治疗效果。等量剂量的脂质体药物(10mg/kg体重)在从所研究的各个器官中清除细菌方面更有效,特别是从肝脏中清除。此外,由于脂质体药物毒性降低,可以给予更高的剂量,导致肝脏、脾脏和肾脏中的菌落形成单位数量显著减少。数据表明,脂质体氯法齐明在治疗MAC感染方面非常有效,即使在播散性感染已经确立后才开始治疗。因此,目前的研究表明脂质体氯法齐明在治疗播散性MAC感染方面具有潜在的应用价值。