← 返回前沿论文

基于 DNA 超分子水凝胶的保护性 NK 细胞储库用于增强三阴性乳腺癌治疗

英文原题:Protective NK Cell Reservoir Based on DNA Supramolecular Hydrogel for Enhanced Triple-Negative Breast Cancer Therapy.

PubMed 2026/09/17(内容时间) Research (Wash D C) Q1 · IF 12.9(JCR 2025)

研究概要

过继性自然杀伤(NK)细胞疗法是治疗三阴性乳腺癌的一种有前景的策略,但其疗效往往受到瘤内持久性差以及在免疫抑制性肿瘤微环境中功能耗竭的限制。

中文摘要

过继性自然杀伤(NK)细胞疗法是治疗三阴性乳腺癌的一种有前景的策略,但其疗效往往受到肿瘤内持久性差以及在免疫抑制性肿瘤微环境中功能耗竭的限制。在此,我们开发了一种基于可注射DNA超分子水凝胶的NK细胞递送平台(NK@DSH),该平台可作为移植NK细胞的保护性储库。DNA超分子水凝胶能够在温和条件下高效包封NK细胞,同时保持细胞活力和功能。体内荧光追踪显示,NK细胞在肿瘤内的持久性延长至7 d,并且肿瘤组织内NK细胞积聚增加。在4T1荷瘤小鼠模型中,NK@DSH比游离NK细胞给药产生更强的肿瘤生长抑制作用,同时全身毒性可忽略不计。这种基于DSH的策略为过继性细胞治疗提供了一个可推广的平台,为克服实体瘤治疗中的细胞持久性障碍提供了新见解。

展开英文摘要原文

Adoptive natural killer (NK) cell therapy represents a promising strategy for triple-negative breast cancer, but its therapeutic efficacy is often limited by poor intratumoral persistence and functional exhaustion within the immunosuppressive tumor microenvironment. Here, we developed an injectable DNA supramolecular hydrogel-based NK cell delivery platform (NK@DSH) that functions as a protective reservoir for transferred NK cells. The DNA supramolecular hydrogel enabled efficient NK cell encapsulation under mild conditions while preserving both cell viability and functionality. In vivo fluorescence tracking demonstrated prolonged intratumoral persistence of NK cells for up to 7 d and increased NK cell accumulation within tumor tissues. In a 4T1 tumor-bearing mouse model, NK@DSH produced stronger tumor growth inhibition than free NK cell administration while showing negligible systemic toxicity. This DSH-based strategy provides a generalizable platform for adoptive cell therapy, offering new insights into overcoming cell-persistence barriers in the treatment of solid tumors.

论文信息

作者
Lu W、Li M、He W、Yang W、Fan J、Chen H、Feng C、Yang F
第一作者单位
Department of Oncology, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, P.R. China.China
通讯作者单位
Department of Anesthesiology, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, P.R. China.China
期刊
Research (Washington, D.C.)2026
原文标识
PubMed 42756298 · DOI 10.34133/research.1436