Tomioka H, Sato K, Saito H
Department of Microbiology and Immunology, Shimane Medical University, Izumo, Japan.
Kekkaku. 1991 Dec;66(12):811-7.
Therapeutic efficacy of kanamycin (KM) and clofazimine (CFZ) combined with N2-[(N-acetyl-muramyl)-L-alanyl-D-isoglutaminyl]-N6-stearoyl-L-ly sine, MDP-Lys (L18), against Mycobacterium intracellulare infection induced in mice was studied, based on suppression of incidence of gross lung lesions and bacterial growth at the sites of infection (lungs and spleen), and the following results were obtained. Firstly, KM (0.5 mg) was given sc to mice, daily six times per week in combination (or not) with sc injections of MDP-Lys(18) (0.1 mg) either 1, 3 or 5 times weekly. In this case, KM alone markedly suppressed the incidence of pulmonary gross lesions and the growth of organisms in the lungs and spleen (2-2.5 log-decrease in CFU per organ at week 8) in infected mice. MDP-Lys(18) alone also exhibited similar effect but the efficacy was much lower than that of KM. No synergism was observed for combined use of KM with MDP-Lys(18) in any protocols tested. Secondly, CFZ (0.5 mg) was given to mice by gavage, daily six times per week in combination with or without injections of MDP-Lys(18) (0.1 mg), either 1, 3 or 5 times weekly. In this case, CFZ alone decreased the incidence of gross pulmonary lesions in infected mice and the weaker suppressive effect was noted for MDP-Lys(18) alone. Moreover, CFZ alone suppressed bacterial growth in the lungs and spleen (1.5-2.0 log-decrease in CFU per organ at week 8), while MDP alone failed to cause such a marked reduction in bacterial CFU in the visceral organs.(ABSTRACT TRUNCATED AT 250 WORDS)
基于对小鼠大体肺部病变发生率以及感染部位(肺和脾)细菌生长的抑制作用,研究了卡那霉素(KM)和氯法齐明(CFZ)联合 N2-[(N-乙酰-胞壁酰)-L-丙氨酰-D-异谷氨酰胺基]-N6-硬脂酰-L-赖氨酸,即 MDP-Lys(L18),对小鼠细胞内分枝杆菌感染的治疗效果,并获得了以下结果。首先,给小鼠皮下注射 KM(0.5 毫克),每周六次,同时(或不同时)每周 1、3 或 5 次皮下注射 MDP-Lys(18)(0.1 毫克)。在这种情况下,单独使用 KM 可显著抑制感染小鼠肺部大体病变的发生率以及肺和脾中细菌的生长(第 8 周时每个器官的菌落形成单位减少 2 - 2.5 个对数)。单独使用 MDP-Lys(18)也表现出类似效果,但疗效远低于 KM。在任何测试方案中,KM 与 MDP-Lys(18)联合使用均未观察到协同作用。其次,通过灌胃给小鼠 CFZ(0.5 毫克),每周六次,同时(或不同时)每周 1、3 或 5 次注射 MDP-Lys(18)(0.1 毫克)。在这种情况下,单独使用 CFZ 可降低感染小鼠肺部大体病变的发生率,单独使用 MDP-Lys(18)的抑制作用较弱。此外,单独使用 CFZ 可抑制肺和脾中的细菌生长(第 8 周时每个器官的菌落形成单位减少 1.5 - 2.0 个对数),而单独使用 MDP 未能使内脏器官中的细菌菌落形成单位显著减少。(摘要截断于 250 字)