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血管生成素样 3 衍生物 LNA043 治疗骨关节炎软骨再生:一项随机 1 期试验。

Angiopoietin-like 3-derivative LNA043 for cartilage regeneration in osteoarthritis: a randomized phase 1 trial.

机构信息

Novartis Institutes for BioMedical Research, Basel, Switzerland.

Novartis Pharma, Basel, Switzerland.

出版信息

Nat Med. 2022 Dec;28(12):2633-2645. doi: 10.1038/s41591-022-02059-9. Epub 2022 Dec 1.

DOI:10.1038/s41591-022-02059-9
PMID:36456835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9800282/
Abstract

Osteoarthritis (OA) is a common, debilitating, chronic disease with no disease-modifying drug approved to date. We discovered LNA043-a derivative of angiopoietin-like 3 (ANGPTL3)-as a potent chondrogenesis inducer using a phenotypic screen with human mesenchymal stem cells. We show that LNA043 promotes chondrogenesis and cartilage matrix synthesis in vitro and regenerates hyaline articular cartilage in preclinical OA and cartilage injury models in vivo. LNA043 exerts at least part of these effects through binding to the fibronectin receptor, integrin αβ on mesenchymal stem cells and chondrocytes. In a first-in-human (phase 1), randomized, double-blinded, placebo-controlled, single ascending dose, single-center trial ( NCT02491281 ; sponsored by Novartis Pharmaceuticals), 28 patients with knee OA were injected intra-articularly with LNA043 or placebo (3:1 ratio) either 2 h, 7 d or 21 d before total knee replacement. LNA043 met its primary safety endpoint and showed short serum pharmacokinetics, cartilage penetration and a lack of immunogenicity (secondary endpoints). Post-hoc transcriptomics profiling of cartilage revealed that a single LNA043 injection reverses the OA transcriptome signature over at least 21 d, inducing the expression of hyaline cartilage matrix components and anabolic signaling pathways, while suppressing mediators of OA progression. LNA043 is a novel disease-modifying OA drug candidate that is currently in a phase 2b trial ( NCT04864392 ) in patients with knee OA.

摘要

骨关节炎(OA)是一种常见的、使人虚弱的、慢性疾病,迄今为止尚无批准的疾病修饰药物。我们使用人间质干细胞的表型筛选发现 LNA043-一种血管生成素样 3(ANGPTL3)的衍生物-是一种有效的成软骨诱导剂。我们表明 LNA043 在体外促进成软骨和软骨基质合成,并在体内 OA 和软骨损伤模型中再生透明关节软骨。LNA043 通过与间质干细胞和软骨细胞上的纤维连接蛋白受体整合素 αβ 结合,发挥至少部分这些作用。在一项首次人体(I 期)、随机、双盲、安慰剂对照、单次递增剂量、单中心试验(NCT02491281;由诺华制药公司赞助)中,28 例膝骨关节炎患者在全膝关节置换前 2 小时、7 天或 21 天分别接受 LNA043 或安慰剂(3:1 比例)关节内注射。LNA043 达到了其主要安全性终点,并表现出短暂的血清药代动力学、软骨穿透和缺乏免疫原性(次要终点)。软骨的事后转录组学分析显示,单次 LNA043 注射可至少在 21 天内逆转 OA 转录组特征,诱导透明软骨基质成分和合成代谢信号通路的表达,同时抑制 OA 进展的介质。LNA043 是一种新型的 OA 疾病修饰药物候选物,目前正在进行膝骨关节炎患者的 IIb 期试验(NCT04864392)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/6fcbdd311ec1/41591_2022_2059_Fig12_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/162be2e987ef/41591_2022_2059_Fig9_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/24a072fe7da1/41591_2022_2059_Fig10_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/a3afcbb5adb2/41591_2022_2059_Fig11_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/6fcbdd311ec1/41591_2022_2059_Fig12_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/162be2e987ef/41591_2022_2059_Fig9_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/24a072fe7da1/41591_2022_2059_Fig10_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/a3afcbb5adb2/41591_2022_2059_Fig11_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfdc/9800282/6fcbdd311ec1/41591_2022_2059_Fig12_ESM.jpg

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