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The Cellular Immune Response to Mycobacterium tuberculosis Infection in the Guinea Pig

机译:豚鼠对结核分枝杆菌感染的细胞免疫反应

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Pulmonary tuberculosis in guinea pigs is an extremely useful model for drug and vaccine testing due to the fact that its pathological disease process is similar to that present in humans. Progress in this field has been hindered because the tools necessary to undertake a complete immunological analysis of the guinea pig cellular immune response against Mycobacterium tuberculosis have been lacking. In this study, we combined a new flow cytometric gating strategy with immunohistochemistry to track T cells, B cells, and the MIL4 Ab, which detects both guinea pig heterophils (neutrophils) and eosinophils, to provide the first documentation of the kinetics of influx and positioning of these cell populations. The results show that the responding T cells are mostly CD4 cells and that after day 30 of the infection numbers of these cells in the lungs drops dramatically. These appear to be replaced by a steady increase in B cells and granulocytes which was associated with worsening lung pathology. These data reveal new information about the cellular phenotypes which mediate protective immunity or host immunopathogenesis during M. tuberculosis infection in this key animal model.
机译:豚鼠的肺结核是一种非常有用的药物和疫苗测试模型,因为其病理性疾病过程与人类相似。由于缺乏对豚鼠针对结核分枝杆菌的细胞免疫应答进行完整免疫学分析所需的工具,因此该领域的进展受到了阻碍。在这项研究中,我们将新的流式细胞术门控策略与免疫组化相结合,以追踪T细胞,B细胞和可检测豚鼠异嗜性(嗜中性粒细胞)和嗜酸性粒细胞的MIL4 Ab,从而提供了有关流入和转移动力学的第一份文献。这些细胞群的位置。结果表明,应答的T细胞主要是CD4细胞,感染后第30天,这些细胞在肺中的数量急剧下降。这些似乎被B细胞和粒细胞的稳定增加所取代,而B细胞和粒细胞的稳定增加与肺部病理学恶化有关。这些数据揭示了有关在该关键动物模型中介导结核分枝杆菌感染期间保护性免疫或宿主免疫发病机制的细胞表型的新信息。

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