RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Mechanisms and strategies for reversing NK cell exhaustion in tumor immunotherapy.
Mechanisms and strategies for reversing NK cell exhaustion in tumor immunotherapy.
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自然杀伤(NK)细胞是机体先天免疫系统的重要组成部分,可通过多种杀伤方式靶向多种肿瘤。在研究重点长期集中于T细胞后,NK细胞已成为免疫治疗的重要参与者。近期NK细胞癌症治疗进展,包括过继细胞疗法、免疫检查点抑制、重组细胞因子疗法和纳米药物,已在体内外显示出有希望的结果。随着NK细胞疗法研究不断深入,越来越多证据表明NK细胞会发生表型变化并获得耗竭特征。其主要表现包括增殖能力下降、细胞因子生成减少、受体表达改变,以及淋巴结归巢能力和在肿瘤微环境(TME)中的持续性受损。NK细胞耗竭不仅降低实体瘤治疗中NK细胞的效能和数量,也在治疗耐药和肿瘤细胞逃逸中发挥关键作用。深入理解NK细胞耗竭机制,并制定在抑制性TME中逆转耗竭的策略至关重要。本综述阐述NK细胞成熟和发育过程,重点介绍NK细胞耗竭的表型特征和潜在机制,系统回顾缓解耗竭的方法,并深入讨论NK细胞免疫治疗当前的局限。最终旨在为增强NK细胞癌症治疗提供潜在解决方案和未来方向。
Natural Killer (NK) cells play a crucial role in the body's innate immune system, distinguished by their ability to target a wide array of tumors through diverse killing strategies. Following the intense focus on T cells, NK cells have emerged as a key player in immunotherapy. Recent advancements in NK cell-based cancer treatments, including adoptive cell therapy, immune checkpoint inhibition, recombinant cytokine therapies, and nanomedicines, have demonstrated promising outcomes both in vitro and in vivo. As research into NK cell-based therapies intensifies, evidence is mounting that NK cells undergo phenotypic changes, acquiring characteristics of exhaustion. Key features comprise reduced proliferative capacity, diminished cytokine production, altered receptor expression, as well as compromised lymph node homing and Tumor Microenvironment (TME) persistence.
NK cell exhaustion not only reduces NK cell efficacy and number in solid tumor therapies, but it also plays a crucial role in treatment resistance and tumor cell evasion. Understanding the mechanisms behind NK cell exhaustion and developing strategies to counteract it within the suppressive TME are of paramount importance.
In this review, we delineate the maturation and development of NK cells, emphasize the phenotypic characteristics and underlying mechanisms of NK cell exhaustion, systematically review the methods to mitigate NK cell exhaustion, and thoroughly discuss the current limitations of NK cell immunotherapy. Ultimately, we aim to provide potential solutions and future directions for enhancing NK cell-based cancer treatments.
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