Cancer Research Institute and Department of Medicine, University of California School of Medicine, San Francisco, California 94122.
Infect Immun. 1970 Nov;2(5):601-5. doi: 10.1128/iai.2.5.601-605.1970.
The mechanism by which macrophages kill facultative intracellular parasites is not known. A test system is described utilizing human macrophages derived from blood monocytes and the opportunistic pathogen Listeria monocytogenes. In this system, bacterial killing was impaired under hypoxic conditions. Under aerobic conditions, addition of Clofazimine (B663), a phenazine derivative effective in the treatment of human leprosy, potentiated the killing of Listeria by macrophages. Potentiation occurred at drug concentrations usually attainable in man and which are not directly injurious to the bacteria. The enhanced bactericidal activity occurred only in the presence of oxygen; the drug induced increased leukocyte oxygen consumption which was insensitive to cyanide.
巨噬细胞杀灭兼性细胞内寄生虫的机制尚不清楚。本文描述了一种利用人血液单核细胞来源的巨噬细胞和机会性病原体李斯特菌建立的检测系统。在该系统中,缺氧条件下细菌杀伤作用受损。在需氧条件下,添加苯并嗪衍生物氯法齐明(B663)可增强巨噬细胞对李斯特菌的杀伤作用。增效作用发生在通常可达到的药物浓度,并且对细菌没有直接损伤。增强的杀菌活性仅在存在氧气的情况下发生;药物诱导白细胞耗氧量增加,对氰化物不敏感。