journal article·2024-12-17

Prevent and Reverse Metabolic Dysfunction-Associated Steatohepatitis and Hepatic Fibrosis via mRNA-Mediated Liver-Specific Antibody Therapy

Chenshuang Zhang, Yilong Teng, Xin Bai, Maoping Tang, William Stewart, Jake Jinkun Chen, Xiaoyang Xu, Xue-Qing Zhang

ACS Nano· Volume 18· Issue 50
Publisher page

Abstract

Chronic exposure of the liver to multiple insults culminates in the development of metabolic dysfunction - associated steatohepatitis (MASH), a complicated metabolic syndrome characterized by hepatic steatosis and inflammation, typically accompanied by progressive fibrosis. Despite extensive clinical evaluation, there remain challenges in MASH drug development, which are primarily due to unsatisfactory efficacy and limited specificity. Strategies to address the unmet medical need for MASH with fibrosis before it reaches the irreversible stage of decompensated cirrhosis are critically needed. Herein, we developed an mRNA-mediated liver-specific antibody therapy for MASH and hepatic fibrosis using a targeted lipid nanoparticle (LNP) delivery system. When encapsulated with IL-11 single-chain variable fragment (scFv)-encoded mRNA, the targeted AA3G LNP (termed m IL11-scFv @AA3G) specifically accumulated in the liver and secreted IL-11 scFv to neutralize overexpressed IL-11 in hepatic environments, thus inhibiting the IL-11 signaling pathway in hepatocytes and hepatic stellate cells. As a preventative regimen, systemic administration of m IL11-scFv @AA3G reversed MASH and prevented the progression to fibrosis in a murine model of early MASH. Notably, m IL11-scFv @AA3G exhibited superior efficacy compared to systemic administration of IL-11 scFv alone, attributed to the sustained antibody expression in the liver, which lasted 18-fold longer than that of IL-11 scFv. When tested in the MASH model with fibrosis, m IL11-scFv @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.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Liver Disease Diagnosis and Treatment · Pancreatic function and diabetes · Endoplasmic Reticulum Stress and Disease

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Shanghai Frontiers Science Center of Drug Target Identification and Delivery, School of Pharmaceutical Sciences, National Key Laboratory of Innovative Immunotherapy, Shanghai Jiao Tong University, Shanghai 200240, P. R. China

Department of Chemical and Materials Engineering, New Jersey Institute of Technology, Newark, New Jersey 07102, United States

Department of Biomedical Engineering, New Jersey Institute of Technology, Newark, New Jersey 07102, United States

Division of Oral Biology, School of Dental Medicine and Tufts University, Boston, Massachusetts 02111, United States

Department of Genetics, Molecular and Cell Biology, School of Medicine, Tufts University, Boston, Massachusetts 02111, United States

Funding

Natural Science Foundation of Shanghai Municipality · Shanghai Jiao Tong University · National Key Research and Development Program of China · Gustavus and Louise Pfeiffer Research Foundation · National Natural Science Foundation of China · National Center of Technology Innovation for Biopharmaceuticals · Foundation of National Facility for Translational Medicine (Shanghai )

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