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优化急性髓系白血病中的 NK 细胞治疗

英文原题:Optimizing Natural Killer Cellular Therapy in Acute Myeloid Leukemia.

查看英文原题

Optimizing Natural Killer Cellular Therapy in Acute Myeloid Leukemia.

PubMed 2025/12/03(内容时间) Am J Clin Oncol Q4 · IF 1.8(JCR 2025)

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中文摘要

急性髓系白血病(AML)因其遗传复杂性和对标准治疗易产生耐药,仍然是血液肿瘤学领域的重大难题。即使在治疗方面取得了进展——如大剂量化疗和造血干细胞移植(HSCT)——许多患者的结局仍不理想。近年来,免疫治疗作为一种通过增强机体自身抗白血病防御来提高生存率的策略,已崭露头角。自然杀伤(NK)细胞作为固有免疫的重要组成部分,已显示出无需预先抗原暴露即可直接清除AML细胞的强大潜力。本综述概述了NK细胞在AML免疫监视中的作用、其功能在疾病中受损的机制,以及当前利用NK细胞进行AML管理的治疗策略。我们还讨论了关键障碍和机遇,包括增强NK细胞活性、对抗免疫逃逸和提高治疗持久性的策略。持续的研究对于完善基于NK细胞的疗法并将个体化免疫治疗选择推向更广泛的临床应用至关重要。

展开英文摘要原文

Acute myeloid leukemia (AML) continues to pose a major hurdle in hematologic oncology, driven by its genetic complexity and tendency to resist standard therapies. Even with progress in treatment-such as high-dose chemotherapy and hematopoietic stem cell transplantation (HSCT)-outcomes remain unsatisfactory for many patients. In recent years, immunotherapy has emerged as an appealing strategy to improve survival by strengthening the body's own anti-leukemia defenses.

Natural killer (NK) cells, a critical component of innate immunity, have shown strong potential for directly eliminating AML cells without prior antigen exposure. This review outlines the role of NK cells in AML immune surveillance, mechanisms by which their function becomes impaired in the disease, and the current therapeutic approaches harnessing NK cells in AML management.

We also discuss key obstacles and opportunities, including strategies to boost NK cell activity, counter immune escape, and improve treatment durability. Continued investigation is essential to refine NK cell-based therapies and bring patient-tailored immunotherapeutic options into broader clinical use.

论文信息

作者
George B、Pandey M、Herstein J、Maiti A
第一作者单位
Department of Hematology-Oncology, University of Texas Health Science Center at Houston.United States
通讯作者单位
Department of Leukemia, University of Texas M.D. Anderson Cancer Center, Houston, TX.United States
文献类型
综述
期刊
American journal of clinical oncology2026 May 1
原文标识
PubMed 41332227 · DOI 10.1097/COC.0000000000001262