Jones Gareth W, Jones Simon A
Division of Infection and Immunity, The School of Medicine, Cardiff University, Cardiff, UK.
Immunology. 2016 Feb;147(2):141-51. doi: 10.1111/imm.12554. Epub 2015 Dec 10.
Lymphoid neogenesis is traditionally viewed as a pre-programmed process that promotes the formation of lymphoid organs during development. Here, the spatial organization of T and B cells in lymph nodes and spleen into discrete structures regulates antigen-specific responses and adaptive immunity following immune challenge. However, lymphoid neogenesis is also triggered by chronic or persistent inflammation. Here, ectopic (or tertiary) lymphoid organs frequently develop in inflamed tissues as a response to infection, auto-immunity, transplantation, cancer or environmental irritants. Although these structures affect local immune responses, the contribution of these lymphoid aggregates to the underlining pathology are highly context dependent and can elicit either protective or deleterious outcomes. Here we review the cellular and molecular mechanisms responsible for ectopic lymphoid neogenesis and consider the relevance of these structures in human disease.
传统上认为淋巴新生是一个预先编程的过程,在发育过程中促进淋巴器官的形成。在此过程中,淋巴结和脾脏中T细胞和B细胞的空间组织形成离散结构,调节免疫挑战后的抗原特异性反应和适应性免疫。然而,慢性或持续性炎症也会引发淋巴新生。在此情况下,异位(或三级)淋巴器官经常在发炎组织中形成,以应对感染、自身免疫、移植、癌症或环境刺激物。尽管这些结构会影响局部免疫反应,但这些淋巴聚集物对潜在病理的影响高度依赖于具体情况,可能引发保护性或有害性结果。在此,我们综述了负责异位淋巴新生的细胞和分子机制,并探讨了这些结构在人类疾病中的相关性。