Miao-Miao Hu, Ying Zhao, Nan Zhang, Fang-Yuan Gong, Wei Zhang, Chun-Sheng Dong, Jian-Feng Dai, Jun Wang
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引用次数: 0
摘要
肿瘤微环境(tumor microenvironment, TME)主要由肿瘤细胞、免疫细胞、基质细胞和细胞外成分组成,其复杂的组成和动态变化极大地阻碍了细胞毒性T细胞(cytotoxic T cells, ctl)的效应功能,成为肿瘤免疫治疗的主要障碍。本文就TME中主要成分(不同细胞类型、细胞外基质、营养物质和代谢物等)对T细胞(主要是CD8+ ctl)浸润、存活和效应功能的影响及其机制进行综述和讨论。此外,我们还强调了最近的进展,这些进展可能通过操纵TME内外的成分来增强内源性抗肿瘤免疫,并提高基于t细胞的免疫疗法在癌症患者中的疗效。深入了解TME组分对ctl肿瘤根除能力的影响和作用机制,可能为发现增强内源性抗肿瘤免疫的新靶点和设计联合治疗方案,提高临床肿瘤免疫治疗的疗效铺平道路。
Tumor Microenvironment: Obstacles and Opportunities for T Cell-Based Tumor Immunotherapies.
The complex composition and dynamic change of the tumor microenvironment (TME), mainly consisting of tumor cells, immune cells, stromal cells, and extracellular components, significantly impede the effector function of cytotoxic T lymphocytes (CTL), thus representing a major obstacle for tumor immunotherapies. In this review, we summarize and discuss the impacts and underlying mechanisms of major elements in the TME (different cell types, extracellular matrix, nutrients and metabolites, etc.) on the infiltration, survival, and effector functions of T cells, mainly CD8+ CTLs. Moreover, we also highlight recent advances that may potentiate endogenous antitumor immunity and improve the efficacy of T cell-based immunotherapies in patients with cancer by manipulating components inside/outside of the TME. A deeper understanding of the effects and action mechanisms of TME components on the tumor-eradicating ability of CTLs may pave the way for discovering new targets to augment endogenous antitumor immunity and for designing combinational therapeutic regimens to enhance the efficacy of tumor immunotherapies in the clinic.
期刊介绍:
Molecular Cancer Research publishes articles describing novel basic cancer research discoveries of broad interest to the field. Studies must be of demonstrated significance, and the journal prioritizes analyses performed at the molecular and cellular level that reveal novel mechanistic insight into pathways and processes linked to cancer risk, development, and/or progression. Areas of emphasis include all cancer-associated pathways (including cell-cycle regulation; cell death; chromatin regulation; DNA damage and repair; gene and RNA regulation; genomics; oncogenes and tumor suppressors; signal transduction; and tumor microenvironment), in addition to studies describing new molecular mechanisms and interactions that support cancer phenotypes. For full consideration, primary research submissions must provide significant novel insight into existing pathway functions or address new hypotheses associated with cancer-relevant biologic questions.