Kansal R G, Gomez-Flores R, Sinha I, Mehta R T
Department of Bioimmunotherapy, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Antimicrob Agents Chemother. 1997 Jan;41(1):17-23. doi: 10.1128/AAC.41.1.17.
The therapeutic efficacy of liposomal clofazimine (L-CLF) against Mycobacterium avium complex (MAC) was evaluated in the acute and chronic infection models of the beige mouse (C57BL/6J bgj bgj). The maximum tolerated dose of L-CLF was inversely proportional to the infection level. L-CLF showed higher antibacterial activity than free clofazimine. Treatment with 25 mg of L-CLF per kg of body weight (intravenously) was started at days 1, 8, 15, and 22 postinfection and was studied at three levels of MAC infection (10(4), 10(5), and 10(6) bacilli/mouse). L-CLF treatment caused a significant (P < 0.05 to 0.001) reduction in the numbers of viable bacteria in lung, liver, and spleen at all infection levels, irrespective of time of treatment. However, the best results were obtained when an already established infection was treated (day 22). The organ-related differences in response to the treatment were also affected by the level of infection. A marked reduction in the numbers of CFU was observed in the lungs of mice with lower infection levels, whereas liver and spleen were treated more efficiently at higher infection levels. These studies might help in evaluations of host responses to therapy.
在米色小鼠(C57BL/6J bgj bgj)的急性和慢性感染模型中评估了脂质体氯法齐明(L-CLF)对鸟分枝杆菌复合群(MAC)的治疗效果。L-CLF的最大耐受剂量与感染水平呈反比。L-CLF显示出比游离氯法齐明更高的抗菌活性。在感染后第1、8、15和22天开始以每千克体重25毫克L-CLF(静脉注射)进行治疗,并在三种MAC感染水平(10⁴、10⁵和10⁶杆菌/小鼠)下进行研究。无论治疗时间如何,L-CLF治疗在所有感染水平下均使肺、肝和脾中的活菌数量显著(P < 0.05至0.001)减少。然而,当对已建立的感染进行治疗时(第22天)获得了最佳结果。对治疗反应的器官相关差异也受感染水平的影响。在感染水平较低的小鼠肺中观察到CFU数量显著减少,而在感染水平较高时肝和脾的治疗效果更明显。这些研究可能有助于评估宿主对治疗的反应。