通过mrna介导的肝脏特异性抗体治疗预防和逆转代谢功能障碍相关的脂肪性肝炎和肝纤维化

IF 16 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Chenshuang Zhang, Yilong Teng, Xin Bai, Maoping Tang, William Stewart, Jake Jinkun Chen, Xiaoyang Xu* and Xue-Qing Zhang*, 
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引用次数: 0

摘要

肝脏长期暴露于多种损伤最终导致代谢功能障碍相关脂肪性肝炎(MASH)的发展,这是一种复杂的代谢综合征,以肝脏脂肪变性和炎症为特征,通常伴有进行性纤维化。尽管进行了广泛的临床评估,但MASH药物开发仍然存在挑战,主要是由于疗效不理想和特异性有限。迫切需要在MASH合并纤维化达到失代偿性肝硬化的不可逆阶段之前解决其未满足的医疗需求的策略。在此,我们开发了一种mrna介导的肝脏特异性抗体疗法,用于使用靶向脂质纳米颗粒(LNP)递送系统治疗MASH和肝纤维化。当被IL-11单链可变片段(scFv)编码的mRNA包裹后,靶向的AA3G LNP(称为mIL11-scFv@AA3G)特异性地在肝脏中积累,并分泌IL-11 scFv来中和肝脏环境中过表达的IL-11,从而抑制肝细胞和肝星状细胞中的IL-11信号通路。作为一种预防方案,在小鼠早期MASH模型中,全身给药mIL11-scFv@AA3G逆转了MASH并阻止了纤维化的进展。值得注意的是,mIL11-scFv@AA3G与全身单独给药IL-11 scFv相比,表现出更好的疗效,这是由于抗体在肝脏中的持续表达,比IL-11 scFv持续时间长18倍。当在纤维化的MASH模型中进行测试时,mIL11-scFv@AA3G有效地改善了脂肪变性,解决了纤维化和炎症。这些发现提出了一种针对肝细胞亚型的多功能LNP平台,用于持续表达治疗性抗体来治疗MASH和纤维化。开发的mrna介导的肝脏特异性抗体治疗为解决MASH提供了一种有希望的方法,并具有扩展到各种其他疾病的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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 mIL11-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 mIL11-scFv@AA3G reversed MASH and prevented the progression to fibrosis in a murine model of early MASH. Notably, mIL11-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, mIL11-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.

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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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