一种用于克服非小细胞肺癌治疗中抗原异质性的多靶向 CAR-T 细胞平台
A Multi-Targeting Chimeric Antigen Receptor-T Cell Platform to Overcome Antigen Heterogeneity in the Treatment of Non-Small Cell Lung Cancer.
这些发现支持采用多靶点CAR-T 策略来应对NSCLC及可能其他实体瘤中的抗原异质性。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Phenotypic, functional, and metabolic heterogeneity of immune cells infiltrating non-small cell lung cancer.
Phenotypic, functional, and metabolic heterogeneity of immune cells infiltrating non-small cell lung cancer.
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肺癌是全球发病率最高的癌症,每年新增病例约120万,占全部癌症死亡的17.8%。非小细胞肺癌(NSCLC)约占所有肺癌的85%,死亡率较高,可能与其早期缺乏症状有关,许多患者确诊时肿瘤已转移至其他器官。尽管新疗法改善了患者的长期生存,NSCLC仍难以治愈,疾病控制也不理想。过去20年间,单细胞技术使研究人员能够深入描绘肿瘤微环境(TME)浸润免疫细胞的表型和代谢特征,促进预后预测性生物标志物的发现,并支持新治疗策略的开发。本文讨论主要TIL(肿瘤浸润淋巴细胞)和肿瘤浸润髓系细胞(TIM)亚群的表型和功能特征,以及它们如何促进或抑制NSCLC发生与进展。我们还探讨TIL和TIM生物学中的两个新兴方面:其代谢会影响效应功能、增殖和分化;此外,这些细胞还具有与癌症干细胞相互作用的能力。
Lung cancer is the leading cancer in the world, accounting for 1. 2 million of new cases annually, being responsible for 17. 8% of all cancer deaths. In particular, non-small cell lung cancer (NSCLC) is involved in approximately 85% of all lung cancers with a high lethality probably due to the asymptomatic evolution, leading patients to be diagnosed when the tumor has already spread to other organs. Despite the introduction of new therapies, which have improved the long-term survival of these patients, this disease is still not well cured and under controlled.
Over the past two decades, single-cell technologies allowed to deeply profile both the phenotypic and metabolic aspects of the immune cells infiltrating the TME, thus fostering the identification of predictive biomarkers of prognosis and supporting the development of new therapeutic strategies. In this review, we discuss phenotypic and functional characteristics of the main subsets of tumor-infiltrating lymphocytes (TILs) and tumor-infiltrating myeloid cells (TIMs) that contribute to promote or suppress NSCLC development and progression.
We also address two emerging aspects of TIL and TIM biology, i. e. , their metabolism, which affects their effector functions, proliferation, and differentiation, and their capacity to interact with cancer stem cells.
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