银屑病
免疫系统
DNA
核酸
趋化因子
细胞因子
重编程
脂多糖
巨噬细胞
转录组
免疫学
先天免疫系统
炎症
材料科学
细胞生物学
化学
免疫疗法
癌症研究
获得性免疫系统
生物
自愈水凝胶
肿瘤坏死因子α
作者
Ziang Xu,Zhiqiang Liu,Yijun Li,Yun Wang,X. L. CHEN,Songhang Li,Ye Chen,Lan Yao,Jiale Liang,Yao He,Taoran Tian,Yunfeng Lin
标识
DOI:10.1021/acsami.5c20385
摘要
Psoriasis represents a persistent immune-mediated dermatological disorder for which no curative therapy is currently available, imposing a considerable burden on affected individuals and healthcare resources. And aberrant macrophage activation is one of the main factors influencing the course of psoriasis. However, safe and drug-free strategy to modulate macrophages is still urgently needed. Here, we developed a tetrahedral framework DNA-based hydrogel (TDH), which was constructed via the self-assembly of sticky-ended tetrahedral DNA nanostructures (TDNs). TDH exhibited robust mechanical strength, injectability, and self-healing properties, demonstrating advantages over conventional DNA hydrogels. TDH markedly downregulated pro-inflammatory cytokine and chemokine levels in macrophages activated by lipopolysaccharide (LPS). Furthermore, a widespread reprogramming of inflammatory signaling networks was shown by transcriptome analysis. Clinical symptoms were significantly reduced by topical TDH application in an imiquimod-induced psoriasis mouse model in vivo, which also decreased the infiltration of immune cells and both epidermal hyperplasia, and successfully resulted in immune homeostasis. Importantly, this effect was achieved without systemic toxicity. Collectively, this study establishes TDH as a biocompatible, programmable, and drug-free immunoregulatory platform, which provides a strategy for the application of nucleic acid–based biomaterials in dermatological therapy.
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