Cui Xinyu, Gu Xuanyu, Li Dongyu, Wu Peng, Sun Nan, Zhang Chaoqi, He Jie
Department of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China; 4+4 Medical Doctor Program, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
Department of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, China.
Cancer Lett. 2025 Mar 31;613:217491. doi: 10.1016/j.canlet.2025.217491. Epub 2025 Jan 23.
Tertiary lymphoid structures (TLSs) are ectopic immune cell clusters formed in nonlymphoid tissues affected by persistent inflammation, such as in cancer and prolonged infections. They have features of the structure and function of secondary lymphoid organs, featuring central CD20 B cells, surrounded by CD3 T cells, CD21 follicular dendritic cells, and CD68 macrophages, with a complex vascular system. TLS formation is governed by lymphotoxin-α1β2, TNF, and chemokines like CCL19, CCL21, and CXCL13, differing from secondary lymphoid organ development in developing later in life at sites of chronic inflammation. Their role in enhancing immune responses, particularly in the context of cancer, makes them a focal point in immunotherapy. This review discusses recent advances in TLS assessment that involves complex gene expression signatures, histological analysis, artificial intelligence, and spatial omics. The presence and maturity of TLS are associated with better outcomes in various cancers, acting as a biomarker for immunotherapy effectiveness. This review explores the structure, formation, and role of TLS in disease prognosis, including their roles in immunotherapy and non-immunotherapy treatments, highlighting a need to develop novel techniques for precise characterization of TLS as well as their significance as predictive biomarkers beyond traditional biomarkers.
三级淋巴结构(TLSs)是在受持续性炎症影响的非淋巴组织中形成的异位免疫细胞簇,如在癌症和长期感染中。它们具有二级淋巴器官的结构和功能特征,以中央CD20 B细胞为特征,周围是CD3 T细胞、CD21滤泡树突状细胞和CD68巨噬细胞,并具有复杂的血管系统。TLS的形成受淋巴毒素-α1β2、肿瘤坏死因子(TNF)以及趋化因子(如CCL19、CCL21和CXCL13)的调控,这与二级淋巴器官在生命后期于慢性炎症部位发育不同。它们在增强免疫反应,特别是在癌症背景下的免疫反应中的作用,使其成为免疫治疗的一个焦点。本综述讨论了TLS评估的最新进展,其中涉及复杂的基因表达特征、组织学分析、人工智能和空间组学。TLS的存在和成熟与各种癌症的更好预后相关,可作为免疫治疗有效性的生物标志物。本综述探讨了TLS在疾病预后中的结构、形成和作用,包括它们在免疫治疗和非免疫治疗中的作用,强调需要开发新技术以精确表征TLS及其作为超越传统生物标志物的预测性生物标志物的意义。