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嵌合抗原受体 NK 细胞免疫治疗:现状与前景

英文原题:Immunotherapy of chimeric antigen receptor NK cells: status and its promising future.

查看英文原题

Immunotherapy of chimeric antigen receptor NK cells: status and its promising future.

PubMed 2025/10/30(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)是由胞外抗原识别结构域和多个胞内信号传导结构域组成的基因工程融合蛋白。尽管CAR-T 细胞免疫疗法在治疗血液系统恶性肿瘤方面取得了显著进展,但其在实体瘤中的应用仍不太成功。关键挑战——包括生产复杂性、肿瘤特异性抗原的稀缺以及细胞运输和肿瘤浸润方面的局限性——继续阻碍着治疗效果。自然杀伤(NK)细胞是重要的固有免疫淋巴细胞,在靶向恶性细胞方面发挥着关键作用。其独特的抗原识别机制、强大的细胞毒性和良好的临床安全性使CAR NK细胞成为靶向癌症治疗的一种有前景的替代方案,尤其是对于实体瘤。然而,NK细胞在体内的短暂持久性以及与其制备相关的技术挑战目前限制了该方法的更广泛临床采用。本综述探讨了CAR NK细胞免疫疗法的优势,并综合了当前国内外研究,以推进对CAR NK细胞治疗学的理解。

展开英文摘要原文

Chimeric antigen receptors (CARs) are genetically engineered fusion proteins composed of extracellular antigen-recognition domains and multiple intracellular signaling domains. Although CAR T-cell immunotherapy has achieved significant advancements in treating hematologic malignancies, its application against solid tumors remains less successful.

Key challenges-including production complexities, the scarcity of tumor-specific antigens, and limitations in cell trafficking and tumor infiltration-continue to impede therapeutic efficacy. Natural killer (NK) cells, essential innate immune lymphocytes, play a critical role in targeting malignant cells. Their unique antigen-recognition mechanisms, potent cytotoxicity, and favorable clinical safety profile position CAR NK cells as a promising alternative for targeted cancer therapy, especially for solid tumors.

However, the transient persistence of NK cells in vivo and the technical challenges associated with their preparation currently limit the broader clinical adoption of this approach. This review examines the advantages of CAR NK cells immunotherapy and synthesizes current domestic and international research to advance the understanding of CAR NK cells therapeutics.

论文信息

作者
Wang F、Huang Z、Feng X、Shi M
单位
Department of Hematology, The First Affiliated Hospital of Kunming Medical University, Kunming, China.China
文献类型
综述
期刊
Frontiers in immunology2025
原文标识
PubMed 41246355 · DOI 10.3389/fimmu.2025.1608277