Davis Michael J, Zawieja Scott D, King Philip D
Department of Medical Pharmacology and Physiology, University of Missouri School of Medicine, Columbia, Missouri, USA; email:
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Annu Rev Physiol. 2025 Feb;87(1):151-172. doi: 10.1146/annurev-physiol-022724-104908. Epub 2025 Feb 3.
Two major functions of the lymphatic system are the reabsorption of excess interstitial fluid/protein and the coordination of immune cell interactions and trafficking. Specialized junctions between lymphatic endothelial cells optimize reabsorption. The spontaneous contractions of collecting vessels provide active lymph propulsion. One-way valves prevent backflow, and chemokine gradients direct the migration of immune cells. Specialized compartments within the lymph node facilitate antigen-immune cell interactions to produce innate and acquired immunity. Lymphatic injury and/or mutations in genes controlling vessel/valve development result in contractile/valve dysfunction, reduced immune cell trafficking and, ultimately, lymph-edema. Activated CD4+ T cells produce inflammatory mediators that exacerbate these processes, potentially leading to interstitial and lymphatic vessel remodeling and negatively impacting overall function. Mouse models have advanced our knowledge of lymphatic disease, but clinical trials to reduce the impact of inflammatory mediators have yielded mixed success, implying that additional factors underlying human lymphedema are not yet understood.
淋巴系统的两大主要功能是重吸收多余的组织间液/蛋白质以及协调免疫细胞的相互作用和运输。淋巴管内皮细胞之间的特殊连接优化了重吸收过程。集合淋巴管的自发收缩提供了主动的淋巴推进力。单向瓣膜可防止逆流,趋化因子梯度引导免疫细胞迁移。淋巴结内的特殊区域促进抗原-免疫细胞相互作用,以产生先天性和获得性免疫。淋巴管损伤和/或控制血管/瓣膜发育的基因突变会导致收缩/瓣膜功能障碍、免疫细胞运输减少,并最终导致淋巴水肿。活化的CD4+ T细胞产生炎症介质,加剧这些过程,可能导致组织间隙和淋巴管重塑,并对整体功能产生负面影响。小鼠模型增进了我们对淋巴疾病的了解,但减少炎症介质影响的临床试验结果喜忧参半,这意味着人类淋巴水肿的其他潜在因素尚未被了解。