Lucas Samuel N, Thomas Susan N
Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia 30332, United States of America.
George W. Woodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States of America.
Mol Pharm. 2024 Dec 2;21(12):5929-5943. doi: 10.1021/acs.molpharmaceut.4c00692. Epub 2024 Oct 31.
Intra- and peritumoral lymphatics and tumor-draining lymph nodes play major roles in mediating the adaptive immune response to cancer immunotherapy. Despite this, current paradigms of clinical cancer management seldom seek to therapeutically modulate tumor-lymphatic immune crosstalk. This review explores recent developments that set the stage for how this regulatory axis can be therapeutically manipulated, with a particular emphasis on tumor-localized immunomodulation. Building on this idea, the nature of tumor-lymphatic immune crosstalk and relevant immunotherapeutic targets and pathways are reviewed, with a focus on their translational potential. Engineered drug delivery systems that enhance intratumoral immunotherapy by improving drug delivery to both the tumor and lymph nodes are also highlighted.
肿瘤内及肿瘤周围的淋巴管以及引流肿瘤的淋巴结在介导对癌症免疫疗法的适应性免疫反应中发挥着主要作用。尽管如此,当前临床癌症管理模式很少寻求通过治疗来调节肿瘤-淋巴管免疫串扰。本综述探讨了为如何通过治疗手段操控这一调节轴奠定基础的最新进展,特别强调肿瘤局部免疫调节。基于这一理念,本文回顾了肿瘤-淋巴管免疫串扰的本质以及相关的免疫治疗靶点和途径,重点关注它们的转化潜力。还强调了通过改善药物向肿瘤和淋巴结的递送从而增强肿瘤内免疫治疗的工程化药物递送系统。
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