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可注射瞬时刺激性水凝胶生态位递送 CAR-T 细胞改善实体瘤治疗

英文原题:Delivery of CAR-T cells in a transient injectable stimulatory hydrogel niche improves treatment of solid tumors.

查看英文原题

Delivery of CAR-T cells in a transient injectable stimulatory hydrogel niche improves treatment of solid tumors.

PubMed 2022/04/08(内容时间) Sci Adv Q1 · IF 13.9(JCR 2025)

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中文摘要

过继性细胞治疗(ACT)已被证明在治疗血液肿瘤方面高度有效,但传统的ACT方法在临床上治疗实体瘤效果不佳。与标准静脉给药方法相比,治疗性细胞的新型递送方法在实体瘤治疗中显示出前景,但少数已报道的方法利用了制造复杂且主要在肿瘤切除后或免疫豁免组织中证明适用性的生物材料。在此,我们设计了易于实施的注射用水凝胶,用于CAR-T 细胞和刺激性细胞因子的受控共递送,从而改善实体瘤的治疗。该材料独特的结构同时抑制了包封细胞因子的被动扩散,并允许包封细胞的主动运动,从而实现CAR-T 细胞的长期滞留、活力和激活。给药后产生的短暂炎症微环境提供了CAR-T 细胞的持续暴露,诱导肿瘤反应性CAR-T 表型,并提高治疗效果。

展开英文摘要原文

Adoptive cell therapy (ACT) has proven to be highly effective in treating blood cancers, but traditional approaches to ACT are poorly effective in treating solid tumors observed clinically. Novel delivery methods for therapeutic cells have shown promise for treatment of solid tumors when compared with standard intravenous administration methods, but the few reported approaches leverage biomaterials that are complex to manufacture and have primarily demonstrated applicability following tumor resection or in immune-privileged tissues.

Here, we engineer simple-to-implement injectable hydrogels for the controlled co-delivery of CAR-T cells and stimulatory cytokines that improve treatment of solid tumors. The unique architecture of this material simultaneously inhibits passive diffusion of entrapped cytokines and permits active motility of entrapped cells to enable long-term retention, viability, and activation of CAR-T cells.

The generation of a transient inflammatory niche following administration affords sustained exposure of CAR-T cells, induces a tumor-reactive CAR-T phenotype, and improves efficacy of treatment.

论文信息

作者
Grosskopf AK、Labanieh L、Klysz DD、Roth GA、Xu P、Adebowale O、Gale EC、Jons CK
第一作者单位
Department of Chemical Engineering, Stanford University, Stanford, CA 94305, USA.United States
通讯作者单位
Department of Bioengineering, Stanford University, Stanford, CA 94305, USA.United States
期刊
Science advances2022 Apr 8
原文标识
PubMed 35394838 · DOI 10.1126/sciadv.abn8264