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In vitro quantitation of cell-mediated immunity in guinea-pigs by macrophage reduction of nitro-blue tetrazolium.

机译:通过巨噬细胞还原硝基硝基四唑鎓对豚鼠细胞介导的免疫力的体外定量。

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摘要

In the cell-mediated immune (CMI) system lymphocytes from sensitized animals incubated with antigen manufacture and release lymphokines which activate the hexose-monophosphate shunt in macrophages. The rate-limiting enzyme of this activation is NADPH oxidase, the activity of which can be quantitated by the amount of nitro-blue tetrazolium reduced to formazan, a blue precipitate. Data is presented which demonstrates that lymphokine-activated macrophages can be microscopically quantitated, both in the direct and indirect assays, by counting the number of macrophages containing formazan precipitate. The indirect component of this assay correlates directly to the skin test diameter. Further, it correlates better to the skin test than another assay for CMI, the macrophages aggregation factor assay. The simplicity and reproducibility of this assay provides another method whereby lymphokine activation of physiological events in macrophages can be determined.
机译:在细胞介导的免疫(CMI)系统中,来自致敏动物的淋巴细胞与抗原制造物一起孵育并释放淋巴因子,从而激活巨噬细胞中的己糖一磷酸旁路。该活化的限速酶是NADPH氧化酶,其活性可以通过还原成蓝色沉淀的甲maz的硝基蓝四唑的量来定量。所提供的数据表明,通过计数含有甲precipitate沉淀物的巨噬细胞的数量,可以在直接和间接测定中通过显微镜对淋巴因子激活的巨噬细胞进行显微镜定量。该测定法的间接成分与皮肤测试直径直接相关。此外,它比另一种CMI检测方法巨噬细胞聚集因子检测方法与皮肤测试的相关性更好。该测定法的简单性和可重复性提供了另一种方法,通过该方法可以确定巨噬细胞中生理事件的淋巴因子激活。

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