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基于 PEO-PPO-PEO 聚氧丙烯醚的温敏水凝胶用于控制重组腺相关病毒载体的原位释放,以有效治疗软骨缺损的基因治疗。

Thermosensitive Hydrogel Based on PEO-PPO-PEO Poloxamers for a Controlled In Situ Release of Recombinant Adeno-Associated Viral Vectors for Effective Gene Therapy of Cartilage Defects.

机构信息

Center of Experimental Orthopaedics, Saarland University Medical Center and Saarland University, D-66421, Homburg, Saarland, Germany.

Department of Orthopaedic Surgery, Saarland University Medical Center and Saarland University, D-66421, Homburg, Saarland, Germany.

出版信息

Adv Mater. 2020 Jan;32(2):e1906508. doi: 10.1002/adma.201906508. Epub 2019 Nov 25.

DOI:10.1002/adma.201906508
PMID:31763733
Abstract

Advanced biomaterial-guided delivery of gene vectors is an emerging and highly attractive therapeutic solution for targeted articular cartilage repair, allowing for a controlled and minimally invasive delivery of gene vectors in a spatiotemporally precise manner, reducing intra-articular vector spread and possible loss of the therapeutic gene product. As far as it is known, the very first successful in vivo application of such a biomaterial-guided delivery of a potent gene vector in an orthotopic large animal model of cartilage damage is reported here. In detail, an injectable and thermosensitive hydrogel based on poly(ethylene oxide) (PEO)-poly(propylene oxide) (PPO)-PEO poloxamers, capable of controlled release of a therapeutic recombinant adeno-associated virus (rAAV) vector overexpressing the chondrogenic sox9 transcription factor in full-thickness chondral defects, is applied in a clinically relevant minipig model in vivo. These comprehensive analyses of the entire osteochondral unit with multiple standardized evaluation methods indicate that rAAV-FLAG-hsox9/PEO-PPO-PEO hydrogel-augmented microfracture significantly improves cartilage repair with a collagen fiber orientation more similar to the normal cartilage and protects the subchondral bone plate from early bone loss.

摘要

先进的生物材料引导基因载体的传递是一种新兴的、极具吸引力的靶向关节软骨修复治疗方法,它能够以时空精确的方式控制和微创地传递基因载体,减少关节内载体的扩散和治疗基因产物的可能损失。据目前所知,这里首次报道了在关节软骨损伤的原位大动物模型中,成功应用这种生物材料引导传递强效基因载体的首例体内应用。具体来说,一种可注射的、温敏性的基于聚(氧化乙烯)(PEO)-聚(氧化丙烯)(PPO)-PEO 聚氧乙烯醚的水凝胶,能够在全层软骨缺损中控制释放过表达软骨形成 Sox9 转录因子的治疗性重组腺相关病毒(rAAV)载体,在临床相关小型猪模型中进行了体内应用。这些通过多种标准化评估方法对整个骨软骨单位进行的综合分析表明,rAAV-FLAG-hsox9/PEO-PPO-PEO 水凝胶增强微骨折术可显著改善软骨修复,使胶原纤维方向更接近正常软骨,并防止软骨下骨板早期丢失。

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