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一种新型针对血管生成素样蛋白 3 的纳米抗体重链抗体可降低血浆脂质并缓解非酒精性脂肪性肝病。

A novel nanobody-heavy chain antibody against Angiopoietin-like protein 3 reduces plasma lipids and relieves nonalcoholic fatty liver disease.

机构信息

School of Pharmacy & Minhang Hospital, Shanghai Engineering Research Center of Immunotherapeutic, Fudan University, Shanghai, 201203, China.

National Children's Medical Center, Children's Hospital of Fudan University, Shanghai, 201203, China.

出版信息

J Nanobiotechnology. 2022 May 19;20(1):237. doi: 10.1186/s12951-022-01456-z.

Abstract

BACKGROUND

Nonalcoholic fatty liver disease (NAFLD) is a metabolic disease mainly on account of hypercholesterolemia and may progress to cirrhosis and hepatocellular carcinoma. The discovery of effective therapy for NAFLD is an essential unmet need. Angiopoietin-like protein 3 (ANGPTL3), a critical lipid metabolism regulator, resulted in increased blood lipids and was elevated in NAFLD. Here, we developed a nanobody-heavy chain antibody (VHH-Fc) to inhibit ANGPTL3 for NAFLD treatment.

RESULTS

In this study, we retrieved an anti-ANGPTL3 VHH and Fc fusion protein, C44-Fc, which exhibited high affinities to ANGPTL3 proteins and rescued ANGPLT3-mediated inhibition of lipoprotein lipase (LPL) activity. The C44-Fc bound a distinctive epitope within ANGPTL3 when compared with the approved evinacumab, and showed higher expression yield. Meanwhile, C44-Fc had significant reduction of the triglyceride (~ 44.2%), total cholesterol (~ 36.6%) and LDL-cholesterol (~ 54.4%) in hypercholesterolemic mice and ameliorated hepatic lipid accumulation and liver injury in NAFLD mice model.

CONCLUSIONS

We discovered a VHH-Fc fusion protein with high affinity to ANGPTL3, strong stability and also alleviated the progression of NAFLD, which might offer a promising therapy for NAFLD.

摘要

背景

非酒精性脂肪性肝病(NAFLD)是一种主要由高胆固醇血症引起的代谢性疾病,可能进展为肝硬化和肝细胞癌。发现有效的 NAFLD 治疗方法是一个亟待满足的需求。血管生成素样蛋白 3(ANGPTL3)是一种关键的脂质代谢调节剂,可导致血脂升高,并在 NAFLD 中升高。在这里,我们开发了一种针对 ANGPTL3 的纳米抗体重链抗体(VHH-Fc)用于治疗 NAFLD。

结果

在这项研究中,我们检索到一种抗 ANGPTL3 的 VHH 和 Fc 融合蛋白 C44-Fc,它对 ANGPTL3 蛋白具有高亲和力,并挽救了 ANGPLT3 介导的脂蛋白脂肪酶(LPL)活性抑制。与已批准的evinacumab 相比,C44-Fc 结合了 ANGPTL3 内的一个独特表位,并且表达产量更高。同时,C44-Fc 可显著降低高脂血症小鼠的甘油三酯(44.2%)、总胆固醇(36.6%)和 LDL-胆固醇(~54.4%),并改善 NAFLD 小鼠模型中的肝脂质蓄积和肝损伤。

结论

我们发现了一种与 ANGPTL3 具有高亲和力、强稳定性的 VHH-Fc 融合蛋白,可缓解 NAFLD 的进展,为 NAFLD 提供了一种有前景的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed12/9118633/6c2adf72f982/12951_2022_1456_Fig1_HTML.jpg

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