首页> 美国卫生研究院文献>Infection and Immunity >T-cell-independent macrophage activation in mice induced with rRNA from Listeria monocytogenes and dimethyldioctadecylammonium bromide.
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T-cell-independent macrophage activation in mice induced with rRNA from Listeria monocytogenes and dimethyldioctadecylammonium bromide.

机译:单核细胞增生李斯特菌和溴化二甲基二十八烷基溴化铵的rRNA诱导的小鼠T细胞非依赖性巨噬细胞活化。

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摘要

Purified rRNA from Listeria monocytogenes or Pseudomonas aeruginosa injected in combination with dimethyldioctadecylammonium bromide (DDA), protects mice nonspecifically against a lethal challenge of various extra- and intracellular bacteria. In the present study vaccination of BALB/c as well as C57BL/Ka mice with listerial RNA-DDA resulted in activation of fixed-tissue macrophages, as measured by an enhanced in vivo L. monocytogenes killing in spleen and liver. Evidence was found that macrophage activation by vaccination with rRNA-DDA occurred by a T-cell-independent mechanism. Treatment of mice with cyclosporin A had no effect on the enhanced L. monocytogenes killing induced with RNA-DDA; in vitro exposure of RNA-DDA to spleen cell cultures did not give rise to any lymphocyte proliferation. No evidence could be found for a possible adjuvant activity for RNA-DDA in cellular responses; in fact, RNA-DDA had an inhibitory effect on lymphocyte proliferative responses to Listeria antigen and to concanavalin A.
机译:从单核细胞增生性李斯特菌或铜绿假单胞菌与溴化二甲基二十八烷基溴化铵(DDA)一起注射纯化的rRNA,可以非特异性地保护小鼠免受各种细胞外和细胞内细菌的致死性攻击。在本研究中,用利斯特氏菌RNA-DDA对BALB / c以及C57BL / Ka小鼠进行疫苗接种可导致固定组织巨噬细胞的活化,这通过增强的体内单核细胞增生李斯特氏菌在脾脏和肝脏中的杀伤力来衡量。有证据表明,通过接种rRNA-DDA激活巨噬细胞是通过非T细胞机制引起的。用环孢菌素A处理小鼠对RNA-DDA诱导的单核细胞增生李斯特菌杀伤力增强没有影响。 RNA-DDA在体外暴露于脾细胞培养物中不会引起任何淋巴细胞增殖。没有证据表明RNA-DDA在细胞反应中可能具有佐剂活性。事实上,RNA-DDA对李斯特菌抗原和伴刀豆球蛋白A的淋巴细胞增殖反应具有抑制作用。

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