Immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancer

Abstract Background Tertiary lymphoid structures (TLS) correlate with tumour prognosis and immunotherapy responses in gastric cancer (GC) studies. However, understanding the complex and diverse immune microenvironment within TLS requires comprehensive analysis. Methods We examined the prognostic imp...

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Main Authors: Yi Xie, Haoxin Peng, Yajie Hu, Keren Jia, Jiajia Yuan, Dan Liu, Yanyan Li, Xujiao Feng, Jian Li, Xiaotian Zhang, Yu Sun, Lin Shen, Yang Chen
Format: Article
Language:English
Published: BMC 2025-02-01
Series:BMC Medicine
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Online Access:https://doi.org/10.1186/s12916-025-03889-3
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author Yi Xie
Haoxin Peng
Yajie Hu
Keren Jia
Jiajia Yuan
Dan Liu
Yanyan Li
Xujiao Feng
Jian Li
Xiaotian Zhang
Yu Sun
Lin Shen
Yang Chen
author_facet Yi Xie
Haoxin Peng
Yajie Hu
Keren Jia
Jiajia Yuan
Dan Liu
Yanyan Li
Xujiao Feng
Jian Li
Xiaotian Zhang
Yu Sun
Lin Shen
Yang Chen
author_sort Yi Xie
collection DOAJ
description Abstract Background Tertiary lymphoid structures (TLS) correlate with tumour prognosis and immunotherapy responses in gastric cancer (GC) studies. However, understanding the complex and diverse immune microenvironment within TLS requires comprehensive analysis. Methods We examined the prognostic impact of TLS within the tumour core (TC) of 59 GC patients undergoing immunotherapy. Multispectral fluorescence imaging was employed to evaluate variations in immune cell infiltration across different TLS sites among 110 GC patients, by quantifying immune cell density and spatial characteristics. We also generated a single-cell transcriptomic atlas of TLS-positive (n = 4) and TLS-negative (n = 8) microenvironments and performed spatial transcriptomics (ST) analysis on two samples. Results TLS presence in the TC significantly correlated with improved immune-related overall survival (P = 0.049). CD8+LAG-3−PD-1+TIM-3−, CD4+PD-L1+, and CD4+FoxP3− T cell densities were significantly higher in the TLS within TC compared to tumour and stromal regions. Immune cells within TLS exhibited closer intercellular proximity than those outside TLS. Five key density and spatial characteristics of immune cells within TLS in the TC were selected to develop the Density and Spatial Score risk model. Single-cell RNA sequencing revealed strong intercellular interactions in the presence of TLS within the microenvironment. However, TLS-absent environment facilitated tumour cell interactions with immune cells through MIF- and galectin-dependent pathways, recruiting immunosuppressive cells. ST analysis confirmed that T and B cells co-localise within TLS, enhancing immune response activation compared to cancer nests and exerting a strong anti-tumour effect. Conclusions TLS presence facilitates frequent cell-to-cell communication, forming an active immune microenvironment, highlighting the prognostic value of TLS.
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spelling doaj-art-812d1dd5b7b64dfba8e6016970b6820c2025-02-09T12:41:00ZengBMCBMC Medicine1741-70152025-02-0123111810.1186/s12916-025-03889-3Immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancerYi Xie0Haoxin Peng1Yajie Hu2Keren Jia3Jiajia Yuan4Dan Liu5Yanyan Li6Xujiao Feng7Jian Li8Xiaotian Zhang9Yu Sun10Lin Shen11Yang Chen12Department of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Pathology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Pathology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteDepartment of Gastrointestinal Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and InstituteAbstract Background Tertiary lymphoid structures (TLS) correlate with tumour prognosis and immunotherapy responses in gastric cancer (GC) studies. However, understanding the complex and diverse immune microenvironment within TLS requires comprehensive analysis. Methods We examined the prognostic impact of TLS within the tumour core (TC) of 59 GC patients undergoing immunotherapy. Multispectral fluorescence imaging was employed to evaluate variations in immune cell infiltration across different TLS sites among 110 GC patients, by quantifying immune cell density and spatial characteristics. We also generated a single-cell transcriptomic atlas of TLS-positive (n = 4) and TLS-negative (n = 8) microenvironments and performed spatial transcriptomics (ST) analysis on two samples. Results TLS presence in the TC significantly correlated with improved immune-related overall survival (P = 0.049). CD8+LAG-3−PD-1+TIM-3−, CD4+PD-L1+, and CD4+FoxP3− T cell densities were significantly higher in the TLS within TC compared to tumour and stromal regions. Immune cells within TLS exhibited closer intercellular proximity than those outside TLS. Five key density and spatial characteristics of immune cells within TLS in the TC were selected to develop the Density and Spatial Score risk model. Single-cell RNA sequencing revealed strong intercellular interactions in the presence of TLS within the microenvironment. However, TLS-absent environment facilitated tumour cell interactions with immune cells through MIF- and galectin-dependent pathways, recruiting immunosuppressive cells. ST analysis confirmed that T and B cells co-localise within TLS, enhancing immune response activation compared to cancer nests and exerting a strong anti-tumour effect. Conclusions TLS presence facilitates frequent cell-to-cell communication, forming an active immune microenvironment, highlighting the prognostic value of TLS.https://doi.org/10.1186/s12916-025-03889-3Gastric cancerTertiary lymphoid structuresTumour microenvironmentImmunotherapyPrognostic modelSingle-cell RNA sequencing
spellingShingle Yi Xie
Haoxin Peng
Yajie Hu
Keren Jia
Jiajia Yuan
Dan Liu
Yanyan Li
Xujiao Feng
Jian Li
Xiaotian Zhang
Yu Sun
Lin Shen
Yang Chen
Immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancer
BMC Medicine
Gastric cancer
Tertiary lymphoid structures
Tumour microenvironment
Immunotherapy
Prognostic model
Single-cell RNA sequencing
title Immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancer
title_full Immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancer
title_fullStr Immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancer
title_full_unstemmed Immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancer
title_short Immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancer
title_sort immune microenvironment spatial landscapes of tertiary lymphoid structures in gastric cancer
topic Gastric cancer
Tertiary lymphoid structures
Tumour microenvironment
Immunotherapy
Prognostic model
Single-cell RNA sequencing
url https://doi.org/10.1186/s12916-025-03889-3
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