Remodelling hypoxic TNBC microenvironment restores antitumor efficacy of Vγ9Vδ2 T cell therapy.

IF 6.4 1区 医学 Q1 ONCOLOGY
Yanyun Jing, Yangzhe Wu, Qinglin Hu, Wenfeng Wu, Dang Li, Wenhao Hu, Heming Li, Minggang Fu, Xin Huang, Yi Hu
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引用次数: 0

Abstract

Background: γδ T cells have emerged as pivotal regulators within the breast cancer tumour microenvironment (TME) and represent a promising therapeutic strategy for late-stage and metastatic breast cancer. In recent years, our research has focused on leveraging allogeneic Vγ9Vδ2 T cells as a novel approach to treat advanced cancers, including triple-negative breast cancer (TNBC). However, the varying clinical outcomes of this therapy have prompted us to investigate the diverse roles of γδ T cells within the TNBC microenvironment and to explore strategies for enhancing therapeutic efficacy through microenvironmental remodelling.

Methods: Data from TCGA, publicly available scRNA-seq datasets and a series of experiments including flow cytometry, atomic force microscopy, confocal laser scanning microscopy, mouse model and others were applied to examine the functional heterogeneity of γδ T cells in TNBC, non-TNBC, and healthy individuals.

Results: γδ T cells serve as predictive markers of better prognosis in breast cancer. In TNBC tumours, γδ T cells exhibited heightened expression of genes linked to both effector and inhibitory molecules, alongside a significant upregulation of glycolytic activity-patterns not observed in non-TNBC or normal breast tissues. Further analysis demonstrated that hypoxic conditions in the TNBC microenvironment likely contribute to these metabolic changes, leading to upregulation of inhibitory checkpoints and downregulation of effector functions in γδ T cells. Importantly, we showed that suppressing HIF-1 signalling using PX478 enhanced the antitumor efficacy of Vδ2+γδ T cell therapy in TNBC-bearing mice.

Discussion: This work underscores that remodelling the hypoxic TNBC microenvironment can restore the antitumor activity of Vγ9Vδ2 T cell therapy. Our findings offer a compelling new adjuvant strategy to improve the outcomes of Vγ9Vδ2 T cell-based therapies for advanced breast cancer treatment.

重塑缺氧TNBC微环境可恢复v - γ - 9v - δ2 T细胞治疗的抗肿瘤效果。
背景:γδ T细胞已成为乳腺癌肿瘤微环境(TME)中的关键调节因子,并代表了晚期和转移性乳腺癌的一种有希望的治疗策略。近年来,我们的研究重点是利用异体Vγ9Vδ2 T细胞作为治疗晚期癌症的新方法,包括三阴性乳腺癌(TNBC)。然而,这种治疗的不同临床结果促使我们研究γδ T细胞在TNBC微环境中的不同作用,并探索通过微环境重塑提高治疗效果的策略。方法:采用TCGA数据、公开的scRNA-seq数据集以及流式细胞术、原子力显微镜、共聚焦激光扫描显微镜、小鼠模型等一系列实验,研究TNBC、非TNBC和健康个体γδ T细胞功能的异质性。结果:γδ T细胞可作为乳腺癌预后较好的预测指标。在TNBC肿瘤中,γδ T细胞表现出与效应分子和抑制分子相关的基因表达升高,同时糖酵解活性显著上调,这在非TNBC或正常乳腺组织中没有观察到。进一步的分析表明,TNBC微环境中的缺氧条件可能有助于这些代谢变化,导致γδ T细胞中抑制检查点的上调和效应功能的下调。重要的是,我们发现使用PX478抑制HIF-1信号传导可增强Vδ2+γδ T细胞治疗tnbc小鼠的抗肿瘤效果。讨论:这项工作强调了重塑缺氧TNBC微环境可以恢复Vγ9Vδ2 T细胞治疗的抗肿瘤活性。我们的研究结果提供了一种令人信服的新辅助策略,以改善基于v γ - 9v - δ2 T细胞的晚期乳腺癌治疗的结果。
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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来源期刊
British Journal of Cancer
British Journal of Cancer 医学-肿瘤学
CiteScore
15.10
自引率
1.10%
发文量
383
审稿时长
6 months
期刊介绍: The British Journal of Cancer is one of the most-cited general cancer journals, publishing significant advances in translational and clinical cancer research.It also publishes high-quality reviews and thought-provoking comment on all aspects of cancer prevention,diagnosis and treatment.
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