| Literature DB >> 34723467 |
Wei Li1, Chengshi Wang1,2, Hui Lv3,4, Zhenghao Wang1,5, Meng Zhao2, Shuyun Liu2, Liping Gou1, Ye Zhou1, Juan Li1, Jiayi Zhang1, Lan Li2, Yizhuo Wang2, Peng Lou2, Lei Wu6, Li Zhou6, Younan Chen2, Yanrong Lu2, Jingqiu Cheng2, Yuan-Ping Han7, Qi Cao8, Wei Huang9, Nanwei Tong1, Xianghui Fu10, Jingping Liu2, Xiaofeng Zheng1, Per-Olof Berggren1,5.
Abstract
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.Entities:
Keywords: DNA nanoraft; DNA origami; acute kidney injury; cytokines; drug delivery carrier; interleukin-33
Year: 2021 PMID: 34723467 DOI: 10.1021/acsnano.1c07270
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881