CNRS, Institut de Pharmacologie et de Biologie Structurale Toulouse, France ; Institut de Pharmacologie et de Biologie Structurale, Université de Toulouse, Université Paul Sabatier Toulouse, France.
Front Immunol. 2013 Jan 7;3:405. doi: 10.3389/fimmu.2012.00405. eCollection 2012.
The granuloma is an elaborated aggregate of immune cells found in non-infectious as well as infectious diseases. It is a hallmark of tuberculosis (TB). Predominantly thought as a host-driven strategy to constrain the bacilli and prevent dissemination, recent discoveries indicate the granuloma can also be modulated into an efficient tool to promote microbial pathogenesis. The aim of future studies will certainly focus on better characterization of the mechanisms driving the modulation of the granuloma functions. Here, we provide unique perspectives from both the innate and adaptive immune system in the formation and the role of the TB granuloma. As macrophages (Mϕs) comprise the bulk of granulomas, we highlight the emerging concept of Mϕ polarization and its potential impact in the microbicide response, and other activities, that may ultimately shape the fate of granulomas. Alternatively, we shed light on the ability of B-cells to influence inflammatory status within the granuloma.
肉芽肿是一种在非传染性和传染性疾病中发现的精心聚集的免疫细胞。它是结核病(TB)的标志。人们普遍认为,肉芽肿主要是一种宿主驱动的策略,用于限制细菌并防止传播,但最近的发现表明,肉芽肿也可以被调节为促进微生物发病机制的有效工具。未来研究的目标肯定将集中在更好地描述驱动肉芽肿功能调节的机制上。在这里,我们从先天和适应性免疫系统两个方面提供了有关 TB 肉芽肿的形成和作用的独特视角。由于巨噬细胞(Mϕ)构成了肉芽肿的大部分,因此我们强调了 Mϕ 极化的新兴概念及其在微环境反应和其他可能最终影响肉芽肿命运的活动中的潜在影响。或者,我们阐明了 B 细胞影响肉芽肿内炎症状态的能力。