Vaccine Research Unit, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunidad Valenciana (Fisabio), 46020 Valencia, Spain.
Institute of Pharmaceutical Sciences, ETH Zurich, CH-8093 Zurich, Switzerland.
Cells. 2021 May 20;10(5):1269. doi: 10.3390/cells10051269.
Afferent lymphatic vessels (LVs) mediate the transport of antigen and leukocytes to draining lymph nodes (dLNs), thereby serving as immunologic communication highways between peripheral tissues and LNs. The main cell types migrating via this route are antigen-presenting dendritic cells (DCs) and antigen-experienced T cells. While DC migration is important for maintenance of tolerance and for induction of protective immunity, T cell migration through afferent LVs contributes to immune surveillance. In recent years, great progress has been made in elucidating the mechanisms of lymphatic migration. Specifically, time-lapse imaging has revealed that, upon entry into capillaries, both DCs and T cells are not simply flushed away with the lymph flow, but actively crawl and patrol and even interact with each other in this compartment. Detachment and passive transport to the dLN only takes place once the cells have reached the downstream, contracting collecting vessel segments. In this review, we describe how the anatomy of the lymphatic network supports leukocyte trafficking and provide updated knowledge regarding the cellular and molecular mechanisms responsible for lymphatic migration of DCs and T cells. In addition, we discuss the relevance of DC and T cell migration through afferent LVs and its presumed implications on immunity.
Afferent lymphatic vessels (LVs) mediate the transport of antigen and leukocytes to draining lymph nodes (dLNs), thereby serving as immunologic communication highways between peripheral tissues and LNs. The main cell types migrating via this route are antigen-presenting dendritic cells (DCs) and antigen-experienced T cells. While DC migration is important for maintenance of tolerance and for induction of protective immunity, T cell migration through afferent LVs contributes to immune surveillance. In recent years, great progress has been made in elucidating the mechanisms of lymphatic migration. Specifically, time-lapse imaging has revealed that, upon entry into capillaries, both DCs and T cells are not simply flushed away with the lymph flow, but actively crawl and patrol and even interact with each other in this compartment. Detachment and passive transport to the dLN only takes place once the cells have reached the downstream, contracting collecting vessel segments. In this review, we describe how the anatomy of the lymphatic network supports leukocyte trafficking and provide updated knowledge regarding the cellular and molecular mechanisms responsible for lymphatic migration of DCs and T cells. In addition, we discuss the relevance of DC and T cell migration through afferent LVs and its presumed implications on immunity.
腔静脉(LVs)介导抗原和白细胞向引流淋巴结(dLNs)的运输,从而充当外周组织和 LNs 之间的免疫通讯高速公路。通过此途径迁移的主要细胞类型是呈递抗原的树突状细胞(DCs)和抗原经验的 T 细胞。虽然 DC 迁移对于维持耐受性和诱导保护性免疫很重要,但 T 细胞通过输入 LVs 的迁移有助于免疫监视。近年来,在阐明淋巴管迁移的机制方面取得了巨大进展。具体来说,延时成像揭示了,一旦进入毛细血管,DC 和 T 细胞就不会简单地随淋巴流被冲走,而是在这个腔室中主动爬行、巡逻,甚至相互作用。只有当细胞到达下游收缩的收集管段时,才会发生与 dLN 的分离和被动运输。在这篇综述中,我们描述了淋巴网络的解剖结构如何支持白细胞的贩运,并提供了有关 DC 和 T 细胞淋巴管迁移所涉及的细胞和分子机制的最新知识。此外,我们还讨论了 DC 和 T 细胞通过输入 LVs 的迁移的相关性及其对免疫的推测影响。