Department of Medicine, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham Alabama, USA.
Department of Molecular Cell Biology and Immunology, VU University Medical Center, Amsterdam, The Netherlands.
Mucosal Immunol. 2014 May;7(3):455-66. doi: 10.1038/mi.2014.11. Epub 2014 Feb 26.
Mucosal surfaces are constantly exposed to environmental antigens, colonized by commensal organisms and used by pathogens as points of entry. As a result, the immune system has devoted the bulk of its resources to mucosal sites to maintain symbiosis with commensal organisms, prevent pathogen entry, and avoid unnecessary inflammatory responses to innocuous antigens. These functions are facilitated by a variety of mucosal lymphoid organs that develop during embryogenesis in the absence of microbial stimulation as well as ectopic lymphoid tissues that develop in adults following microbial exposure or inflammation. Each of these lymphoid organs samples antigens from different mucosal sites and contributes to immune homeostasis, commensal containment, and immunity to pathogens. Here we discuss the mechanisms, mostly based on mouse studies, that control the development of mucosal lymphoid organs and how the various lymphoid tissues cooperate to maintain the integrity of the mucosal barrier.
黏膜表面不断暴露于环境抗原中,被共生生物定植,并被病原体用作入侵点。因此,免疫系统将其大部分资源都用于黏膜部位,以维持与共生生物的共生关系,防止病原体进入,并避免对无害抗原产生不必要的炎症反应。这些功能是通过各种黏膜淋巴器官来实现的,这些器官在胚胎发育过程中在没有微生物刺激的情况下形成,此外,还有异位淋巴组织,它们在成年后受到微生物暴露或炎症的刺激后形成。这些淋巴器官中的每一个都从不同的黏膜部位取样抗原,并有助于免疫稳态、共生生物的控制以及对病原体的免疫。在这里,我们讨论控制黏膜淋巴器官发育的机制,这些机制主要基于小鼠研究,以及各种淋巴组织如何合作来维持黏膜屏障的完整性。