细胞因子
急性肾损伤
免疫疗法
免疫系统
医学
肾
免疫学
癌症研究
内科学
作者
Wei Li,Chengshi Wang,Hui Lv,Zhenghao Wang,Meng Zhao,Shuyun Liu,Liping Gou,Ye Zhou,Juan Li,Jiayi Zhang,Lan Li,Yizhuo Wang,Peng Lou,Lei Wu,Li Zhou,Younan Chen,Yanrong Lu,Jingqiu Cheng,Yuan‐Ping Han,Qi Cao
出处
期刊:ACS Nano
[American Chemical Society]
日期:2021-11-01
卷期号:15 (11): 18237-18249
被引量:43
标识
DOI:10.1021/acsnano.1c07270
摘要
Cytokine immunotherapy represents an attractive strategy to stimulate robust immune responses for renal injury repair in ischemic acute kidney injury (AKI). However, its clinical application is hindered by its nonspecificity to kidney, short circulation half-life, and severe side effects. An ideal cytokine immunotherapy for AKI requires preferential delivery of cytokines with accurate dosage to the kidney and sustained-release of cytokines to stimulate the immune responses. Herein, we developed a DNA nanoraft cytokine by precisely arranging interleukin-33 (IL-33) nanoarray on rectangle DNA origami, through which IL-33 can be preferentially delivered to the kidney for alleviation of AKI. A nanoraft carrying precisely quantified IL-33 predominantly accumulated in the kidney for up to 48 h. Long-term sustained-release of IL-33 from nanoraft induced rapid expansion of type 2 innate lymphoid cells (ILC 2s) and regulatory T cells (Tregs) and achieved better treatment efficiency compared to free IL-33 treatment. Thus, our study demonstrates that a nanoraft can serve as a structurally well-defined delivery platform for cytokine immunotherapy in ischemic AKI and other renal diseases.
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