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孤立淋巴滤泡成熟诱导滤泡树突状细胞发育。

Isolated lymphoid follicle maturation induces the development of follicular dendritic cells.

作者信息

Glaysher Bridget R, Mabbott Neil A

机构信息

Institute for Animal Health, Ogston Building, West Mains Road, Edinburgh, UK.

出版信息

Immunology. 2007 Mar;120(3):336-44. doi: 10.1111/j.1365-2567.2006.02508.x. Epub 2006 Dec 5.

Abstract

Isolated lymphoid follicles (ILFs) are recently identified lymphoid structures in the small intestine with features similar to Peyer's patches (PPs). Using immunohistochemistry we characterized the composition of ILFs in the small intestines of immunocompetent mice and of mice that lacked PPs as a result of either genetic deficiency of lymphotoxin or temporary in utero lymphotoxin-beta receptor-signalling blockade. We showed that although both immature and mature ILFs were present in the intestines of immunocompetent mice, PP-deficiency induced a significantly greater number of mature ILFs. We found that in addition to B-lymphocyte-containing germinal centres, mature ILFs also possessed large networks of follicular dendritic cells (FDCs). These features were not detected within immature ILFs. Indeed, the presence of FDCs could be used to reliably distinguish ILF maturity. Further analysis revealed that the area occupied by the FDCs within mature ILFs was substantial. The total area occupied by FDCs in all the mature ILFs in mice lacking PPs was equivalent to the total area occupied by FDCs in all the PPs and the few mature ILFs in immunocompetent mice. Based on these data we reasoned that in the absence of PPs, mature ILFs are important inductive sites for intestinal immune responses. Indeed, in mice that lacked PPs, ILF maturation coincided with a restoration of faecal immunoglobulin A levels to values that were comparable to those found in immunocompetent mice. Taken together, these data imply that the induction of germinal centres and FDC networks within mature ILFs in response to PP deficiency provides an important compensatory mechanism.

摘要

孤立淋巴滤泡(ILFs)是最近在小肠中发现的淋巴结构,其特征与派尔集合淋巴结(PPs)相似。我们运用免疫组织化学方法,对免疫功能正常小鼠以及因淋巴毒素基因缺陷或子宫内临时淋巴毒素β受体信号阻断而缺乏PPs的小鼠小肠中的ILFs组成进行了表征。我们发现,尽管免疫功能正常小鼠的小肠中同时存在未成熟和成熟的ILFs,但缺乏PPs会导致成熟ILFs的数量显著增加。我们还发现,除了含有B淋巴细胞的生发中心外,成熟ILFs还拥有大量的滤泡树突状细胞(FDCs)网络。这些特征在未成熟ILFs中并未检测到。事实上,FDCs的存在可用于可靠地区分ILF的成熟度。进一步分析表明,成熟ILFs中FDCs所占的面积相当可观。缺乏PPs的小鼠所有成熟ILFs中FDCs所占的总面积,与免疫功能正常小鼠所有PPs和少数成熟ILFs中FDCs所占的总面积相当。基于这些数据,我们推断在缺乏PPs的情况下,成熟ILFs是肠道免疫反应的重要诱导部位。实际上,在缺乏PPs的小鼠中,ILF成熟与粪便免疫球蛋白A水平恢复到与免疫功能正常小鼠相当的值同时发生。综上所述,这些数据表明,响应PP缺乏而在成熟ILFs中诱导生发中心和FDC网络提供了一种重要的补偿机制。

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