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:Dendritic Cell Vaccination in Non-Small Cell Lung Cancer: Remodeling the Tumor Immune Microenvironment.
Dendritic Cell Vaccination in Non-Small Cell Lung Cancer: Remodeling the Tumor Immune Microenvironment.
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非小细胞肺癌(NSCLC)仍然是全球主要死亡原因之一。尽管NSCLC具有可能引发T细胞应答的抗原,但缺陷性肿瘤抗原呈递和T细胞活化阻碍了宿主抗肿瘤免疫应答。NSCLC肿瘤微环境(TME)由可促进或对抗肿瘤生长的细胞和可溶性介质组成。TME的组成在促进肿瘤发生和决定对免疫治疗的抗肿瘤免疫应答中起关键作用。树突状细胞(DC)是激活抗肿瘤T细胞应答并维持效应应答的关键免疫细胞。DC疫苗是一种有前景的细胞免疫疗法,有可能通过肿瘤抗原呈递和细胞间通讯促进抗肿瘤免疫应答并改变NSCLC TME的组成。在此,我们将综述NSCLC TME的特征,重点介绍直接与DC相互作用的免疫细胞表型。此外,我们将总结DC疫苗制备的主要临床前和临床方法,并探讨有效的DC疫苗接种如何将NSCLC TME转变为持续抗肿瘤免疫信号传导的状态。
Non-small-cell lung cancer (NSCLC) remains one of the leading causes of death worldwide. While NSCLCs possess antigens that can potentially elicit T cell responses, defective tumor antigen presentation and T cell activation hinder host anti-tumor immune responses. The NSCLC tumor microenvironment (TME) is composed of cellular and soluble mediators that can promote or combat tumor growth.
The composition of the TME plays a critical role in promoting tumorigenesis and dictating anti-tumor immune responses to immunotherapy. Dendritic cells (DCs) are critical immune cells that activate anti-tumor T cell responses and sustain effector responses. DC vaccination is a promising cellular immunotherapy that has the potential to facilitate anti-tumor immune responses and transform the composition of the NSCLC TME via tumor antigen presentation and cell-cell communication.
Here, we will review the features of the NSCLC TME with an emphasis on the immune cell phenotypes that directly interact with DCs.
Additionally, we will summarize the major preclinical and clinical approaches for DC vaccine generation and examine how effective DC vaccination can transform the NSCLC TME toward a state of sustained anti-tumor immune signaling.
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