肝细胞癌
免疫检查点
封锁
免疫系统
医学
肿瘤科
癌症研究
免疫疗法
免疫学
内科学
受体
作者
Daniel Shu,Won Jin Ho,Luciane T. Kagohara,Alexander Girgis,Sarah M. Shin,Ludmila Danilova,Jae W. Lee,Dimitrios N. Sidiropoulos,Sarah Mitchell,Kabeer Munjal,Kathryn L. Howe,Kayla J. Bendinelli,Hanfei Qi,Guanglan Mo,Janelle M. Montagne,James M. Leatherman,Tamara Y. Lopez-Vidal,Qingfeng Zhu,Amanda L. Huff,Xuan Yuan
出处
期刊:
[Cold Spring Harbor Laboratory]
日期:2023-10-19
被引量:11
标识
DOI:10.1101/2023.10.16.562104
摘要
Neoadjuvant immunotherapy is thought to produce long-term remissions through induction of antitumor immune responses before removal of the primary tumor. Tertiary lymphoid structures (TLS), germinal center-like structures that can arise within tumors, may contribute to the establishment of immunological memory in this setting, but understanding of their role remains limited. Here, we investigated the contribution of TLS to antitumor immunity in hepatocellular carcinoma (HCC) treated with neoadjuvant immunotherapy. We found that neoadjuvant immunotherapy induced the formation of TLS, which were associated with superior pathologic response, improved relapse free survival, and expansion of the intratumoral T and B cell repertoire. While TLS in viable tumor displayed a highly active mature morphology, in areas of tumor regression we identified an involuted TLS morphology, which was characterized by dispersion of the B cell follicle and persistence of a T cell zone enriched for ongoing antigen presentation and T cell-mature dendritic cell interactions. Involuted TLS showed increased expression of T cell memory markers and expansion of CD8
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