Departments of Pediatrics and Pathology, Children's Hospital, The Immune Disease Institute, Program in Cellular and Molecular Medicine, and Harvard Medical School, Boston, Massachusetts, USA.
Adv Immunol. 2010;106:1-19. doi: 10.1016/S0065-2776(10)06001-3.
Over the past decade, it has become apparent that B cells acquire antigens primarily from membrane surfaces and that uptake is an active process involving a synapse between the B cell receptor, coreceptor, and the antigen surface. However, understanding how antigens are delivered to follicular dendritic cells (FDC), which are the primary depot for B cell antigen within the lymph node follicles, is only recently beginning to be dissected. The application of fluorescent-based imaging techniques such as multiphoton intravital microscopy to visualize trafficking of B cells and antigens into draining lymph nodes has provide insights that would not otherwise be made. At least three novel pathways for transport of lymph-borne antigens to the B cell compartment have been identified. Based on these studies, a new paradigm of how lymphocytes and antigens traffic within the peripheral lymph nodes is evolving. Understanding how the physical properties of the antigen influences its uptake and processing could be relevant in the design of new vaccines.
在过去的十年中,人们已经明显认识到 B 细胞主要从细胞膜表面获取抗原,摄取是一个涉及 B 细胞受体、辅助受体和抗原表面之间突触的主动过程。然而,对于抗原如何递呈给滤泡树突状细胞(FDC),即淋巴结滤泡中 B 细胞抗原的主要储存库,人们直到最近才开始进行剖析。荧光基成像技术的应用,如多光子活体显微镜,用于可视化 B 细胞和抗原进入引流淋巴结的运输,提供了其他方法无法获得的见解。至少已经确定了三种将淋巴源抗原运输到 B 细胞区室的新途径。基于这些研究,关于淋巴细胞和抗原在周围淋巴结内如何运输的新范式正在不断发展。了解抗原的物理性质如何影响其摄取和加工可能与新型疫苗的设计相关。