脂肪性肝炎
抗体
医学
肝纤维化
肝功能不全
信使核糖核酸
纤维化
肝纤维化
免疫学
脂肪肝
生物
内科学
生物化学
疾病
基因
作者
Chenshuang Zhang,Yilong Teng,Xin Bai,Maoping Tang,William C. Stewart,Jake Chen,Xiaoyang Xu,Xue‐Qing Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-12-06
卷期号:18 (50): 34375-34390
被引量:17
标识
DOI:10.1021/acsnano.4c13404
摘要
@AA3G effectively ameliorated steatosis and resolved fibrosis and inflammation. These findings present a versatile LNP platform targeting liver cell subtypes for the sustained expression of therapeutic antibodies to treat MASH and fibrosis. The developed mRNA-mediated liver-specific antibody therapy offers a promising approach for addressing MASH and holds the potential for expansion to various other diseases.
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