Silva Miranda Mayra, Breiman Adrien, Allain Sophie, Deknuydt Florence, Altare Frederic
INSERM U892, CNRS UMR 6299, Université de Nantes, 44007 Nantes Cedex 1, France.
Clin Dev Immunol. 2012;2012:139127. doi: 10.1155/2012/139127. Epub 2012 Jul 3.
One of the main features of the immune response to M. Tuberculosis is the formation of an organized structure called granuloma. It consists mainly in the recruitment at the infectious stage of macrophages, highly differentiated cells such as multinucleated giant cells, epithelioid cells and Foamy cells, all these cells being surrounded by a rim of lymphocytes. Although in the first instance the granuloma acts to constrain the infection, some bacilli can actually survive inside these structures for a long time in a dormant state. For some reasons, which are still unclear, the bacilli will reactivate in 10% of the latently infected individuals, escape the granuloma and spread throughout the body, thus giving rise to clinical disease, and are finally disseminated throughout the environment. In this review we examine the process leading to the formation of the granulomatous structures and the different cell types that have been shown to be part of this inflammatory reaction. We also discuss the different in vivo and in vitro models available to study this fascinating immune structure.
对结核分枝杆菌免疫反应的主要特征之一是形成一种称为肉芽肿的组织结构。它主要在于在感染阶段招募巨噬细胞、高度分化的细胞,如多核巨细胞、上皮样细胞和泡沫细胞,所有这些细胞都被一圈淋巴细胞包围。虽然最初肉芽肿的作用是限制感染,但一些杆菌实际上可以在这些结构内长期处于休眠状态存活。由于一些尚不清楚的原因,杆菌会在10%的潜伏感染个体中重新激活,逃离肉芽肿并扩散到全身,从而引发临床疾病,最终传播到整个环境中。在这篇综述中,我们研究了导致肉芽肿结构形成的过程以及已被证明是这种炎症反应一部分的不同细胞类型。我们还讨论了可用于研究这种迷人免疫结构的不同体内和体外模型。