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用于癌症免疫治疗的 CAR-NK 细胞:近期进展与未来方向

英文原题:CAR-NK cells for cancer immunotherapy: recent advances and future directions.

查看英文原题

CAR-NK cells for cancer immunotherapy: recent advances and future directions.

PubMed 2024/02/09(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

自然杀伤(NK)细胞是固有免疫系统的重要组成部分,因其在抗肿瘤免疫应答中具有独立的细胞毒性能力,在抗击癌症中发挥关键作用。与主要靶向T细胞免疫的治疗方法不同,T细胞免疫治疗的有限成功凸显了创新方法的紧迫性,其中NK细胞的潜力备受关注。尽管肿瘤已演化出逃避NK细胞诱导的细胞毒性的机制,但嵌合抗原受体(CAR)NK细胞仍令人乐观。这篇综合性综述深入探讨了NK细胞在肿瘤微环境中动态变化的基础特征及近期突破。文章批判性地评估了新兴CAR-NK细胞治疗策略的潜在应用与挑战,将其定位为不断发展的精准医学领域中颇具前景的工具。随着研究的进展,CAR-NK细胞的独特属性为治疗干预提供了新途径,为更有效、更精准的癌症治疗方法铺平了道路。

展开英文摘要原文

Natural Killer (NK) cells, intrinsic to the innate immune system, are pivotal in combating cancer due to their independent cytotoxic capabilities in antitumor immune response. Unlike predominant treatments that target T cell immunity, the limited success of T cell immunotherapy emphasizes the urgency for innovative approaches, with a spotlight on harnessing the potential of NK cells. Despite tumors adapting mechanisms to evade NK cell-induced cytotoxicity, there is optimism surrounding Chimeric Antigen Receptor (CAR) NK cells.

This comprehensive review delves into the foundational features and recent breakthroughs in comprehending the dynamics of NK cells within the tumor microenvironment. It critically evaluates the potential applications and challenges associated with emerging CAR-NK cell therapeutic strategies, positioning them as promising tools in the evolving landscape of precision medicine.

As research progresses, the unique attributes of CAR-NK cells offer a new avenue for therapeutic interventions, paving the way for a more effective and precise approach to cancer treatment.

论文信息

作者
Li T、Niu M、Zhang W、Qin S、Zhou J、Yi M
第一作者单位
Department of Gynecology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.China
通讯作者单位
Department of Breast Surgery, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.China
文献类型
综述 · 非美国政府资助研究
期刊
Frontiers in immunology2024
原文标识
PubMed 38404574 · DOI 10.3389/fimmu.2024.1361194