Lymphocyte Biology Section, Laboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Lymphocyte Biology Section, Laboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA; Critical Care Medicine Department, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA.
Curr Opin Immunol. 2014 Aug;29:8-15. doi: 10.1016/j.coi.2014.03.002. Epub 2014 Apr 3.
To contain invading microbes, the immune system must efficiently recognize the presence of the invader, mobilize cells to the site of infection, and deploy effector function. Rare antigen-specific T cells must find small numbers of antigen-presenting cells, proliferate and differentiate in secondary lymphoid tissues, then traffic to the infected site and be activated by antigen again to contribute to host defense. Our understanding of the dynamic processes involved has benefited enormously from tools that enable the visualization of cell location and behavior in complex tissue environments. Here we summarize recent insights into T cell trafficking and migration through secondary lymphoid organs and at peripheral infection sites, highlighting cell-intrinsic and extrinsic factors optimizing antigen surveillance at steady-state and delivery of an effector response during infection.
为了遏制入侵的微生物,免疫系统必须有效地识别入侵者的存在,动员细胞到感染部位,并发挥效应功能。罕见的抗原特异性 T 细胞必须找到少量的抗原呈递细胞,在次级淋巴组织中增殖和分化,然后迁移到感染部位,并再次被抗原激活,以有助于宿主防御。我们对涉及的动态过程的理解得益于能够在复杂的组织环境中可视化细胞位置和行为的工具。在这里,我们总结了最近对 T 细胞在次级淋巴器官和外周感染部位的迁移和迁移的深入了解,重点介绍了在稳态时优化抗原监测和在感染时传递效应反应的内在和外在因素。