Amura C R, Fontan P A, Sanjuan N, Sordelli D O
Laboratorio de Bacteriología, Facultad de Medicina, Universidad de Buenos Aires, Argentina.
Clin Immunol Immunopathol. 1994 Nov;73(2):261-6. doi: 10.1006/clin.1994.1196.
The efficacy of treatment with interleukin-1 beta (IL-1 beta) and tumor necrosis factor-alpha (TNF alpha) on Pseudomonas aeruginosa pneumonia was evaluated in a granulocytopenic mouse model. Combined intravenous administration of 2000 U IL-1 beta plus 2000 U TNF alpha significantly diminished mortality from aerosol challenge with P. aeruginosa. Mice treated with IL-1 beta, TNF alpha, or both also exhibited a significant enhancement in pulmonary clearance of P. aeruginosa. Combined cytokine administration induced an increase in the pulmonary content of myeloperoxidase activity. Mature leukocytes were not detected in either circulation or bronchoalveolar lavage fluid from granulocytopenic, cytokine-treated mice. In conclusion, IL-1 beta and TNF alpha treatment exhibited a synergistic protective effect from pulmonary P. aeruginosa challenge in granulocytopenic hosts, probably due to enhancement of nonspecific antibacterial mechanisms.
在粒细胞缺乏的小鼠模型中评估了白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNFα)治疗铜绿假单胞菌肺炎的疗效。联合静脉注射2000 U IL-1β加2000 U TNFα可显著降低铜绿假单胞菌气溶胶攻击所致的死亡率。用IL-1β、TNFα或两者治疗的小鼠在铜绿假单胞菌的肺清除方面也表现出显著增强。联合给予细胞因子可诱导肺髓过氧化物酶活性含量增加。在粒细胞缺乏且接受细胞因子治疗的小鼠的循环系统或支气管肺泡灌洗液中均未检测到成熟白细胞。总之,IL-1β和TNFα治疗对粒细胞缺乏宿主的肺部铜绿假单胞菌攻击具有协同保护作用,这可能是由于非特异性抗菌机制增强所致。