T细胞活化与功能有用的肿瘤相关高内皮小静脉发育之间的联系。

Stefan Milutinovic, Awen Gallimore
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摘要

高内皮小静脉(HEVs)是特化的毛细血管后小静脉,专门用于招募循环淋巴细胞到次要淋巴器官(slo),在次要淋巴器官中可以遇到同源抗原,并启动免疫反应。原发性人实体瘤中hev样血管的存在及其与淋巴细胞浸润的关联、良好的临床结果和对免疫治疗的反应,为在肿瘤中诱导这些血管以获得免疫治疗益处提供了理论依据。在这里,我们特别讨论了t细胞活化和有用的肿瘤相关HEV (TA-HEV)发展之间联系的证据。我们讨论了TA-HEV的分子和功能特征,强调了促进肿瘤免疫的益处,以及在优化TA-HEV诱导以获得免疫治疗益处之前需要解决的重要未解问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The link between T cell activation and development of functionally useful tumour-associated high endothelial venules.

High endothelial venules (HEVs) are specialized postcapillary venules that specifically serve to recruit circulating lymphocytes to secondary lymphoid organs (SLOs) where cognate antigens can be encountered, and immune responses can be initiated. The presence of HEV-like vessels in primary human solid tumours and their association with lymphocyte infiltration and favourable clinical outcomes and response to immunotherapy have provided a rationale for therapeutically inducing these vessels in tumours for immunotherapeutic benefit. Here we specifically discuss evidence for a link between T-cell activation and development of useful tumour-associated HEV (TA-HEV). We discuss the molecular and functional features of TA-HEV, highlighting the benefits for promoting tumour immunity and the important unanswered questions that need to be addressed before TA-HEV induction can be optimized for immunotherapeutic benefit.

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