医学
细胞因子
免疫疗法
全身给药
黑色素瘤
药代动力学
促炎细胞因子
细胞因子释放综合征
免疫学
药理学
癌症研究
免疫系统
炎症
体内
生物
生物技术
嵌合抗原受体
作者
Amanda Nash,Maria Jarvis,Samira Aghlara-Fotovat,Sudip Mukherjee,Andrea Hernández,Andrew D. Hecht,Peter D. Rios,Sofia Ghani,Ira Joshi,Douglas Isa,Yufei Cui,Shirin Nouraein,Jared Z. Lee,Chunyu Xu,David Y. Zhang,Rahul A. Sheth,Weiyi Peng,José Oberholzer,Oleg A. Igoshin,Amir A. Jazaeri
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2022-03-02
卷期号:8 (9)
被引量:51
标识
DOI:10.1126/sciadv.abm1032
摘要
Proinflammatory cytokines have been approved by the Food and Drug Administration for the treatment of metastatic melanoma and renal carcinoma. However, effective cytokine therapy requires high-dose infusions that can result in antidrug antibodies and/or systemic side effects that limit long-term benefits. To overcome these limitations, we developed a clinically translatable cytokine delivery platform composed of polymer-encapsulated human ARPE-19 (RPE) cells that produce natural cytokines. Tumor-adjacent administration of these capsules demonstrated predictable dose modulation with spatial and temporal control and enabled peritoneal cancer immunotherapy without systemic toxicities. Interleukin-2 (IL2)–producing cytokine factory treatment eradicated peritoneal tumors in ovarian and colorectal mouse models. Furthermore, computational pharmacokinetic modeling predicts clinical translatability to humans. Notably, this platform elicited T cell responses in NHPs, consistent with reported biomarkers of treatment efficacy without toxicity. Combined, our findings demonstrate the safety and efficacy of IL2 cytokine factories in preclinical animal models and provide rationale for future clinical testing in humans.
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