Venkatesan Jagadeesh K, Cai Xiaoyu, Meng Weikun, Rey-Rico Ana, Schmitt Gertrud, Speicher-Mentges Susanne, Falentin-Daudré Céline, Leroux Amélie, Madry Henning, Migonney Véronique, Cucchiarini Magali
Center of Experimental Orthopaedics, Université Sorbonne Paris Nord, Villetaneuse, France.
LBPS/CSPBAT UMR CNRS 7244, Université Sorbonne Paris Nord, Villetaneuse, France.
Hum Gene Ther. 2021 Sep;32(17-18):895-906. doi: 10.1089/hum.2020.329. Epub 2021 Apr 26.
Scaffold-guided viral gene therapy is a novel, powerful tool to enhance the processes of tissue repair in articular cartilage lesions by the delivery and overexpression of therapeutic genes in a noninvasive, controlled release manner based on a procedure that may protect the gene vehicles from undesirable host immune responses. In this study, we examined the potential of transferring a recombinant adeno-associated virus (rAAV) vector carrying a sequence for the highly chondroregenerative transforming growth factor beta (TGF-β), using poly(ɛ-caprolactone) (PCL) films functionalized by the grafting of poly(sodium styrene sulfonate) (pNaSS) in chondrogenically competent bone marrow aspirates as future targets for therapy in cartilage lesions. Effective overexpression of TGF-β in the aspirates by rAAV was achieved upon delivery using pNaSS-grafted and ungrafted PCL films for up to 21 days (the longest time point evaluated), with superior levels using the grafted films, compared with respective conditions without vector coating. The production of rAAV-mediated TGF-β by pNaSS-grafted and ungrafted PCL films significantly triggered the biological activities and chondrogenic processes in the samples (proteoglycan and type-II collagen deposition and cell proliferation), while containing premature mineralization and hypertrophy relative to the other conditions, with overall superior effects supported by the pNaSS-grafted films. These observations demonstrate the potential of PCL film-assisted rAAV TGF-β gene transfer as a convenient, off-the-shelf technique to enhance the reparative potential of the bone marrow in patients in future approaches for improved cartilage repair.
支架引导的病毒基因治疗是一种新型的强大工具,它基于一种可保护基因载体免受不良宿主免疫反应影响的程序,以非侵入性、控释方式递送和过表达治疗性基因,从而增强关节软骨损伤的组织修复过程。在本研究中,我们研究了在具有软骨生成能力的骨髓抽吸物中,使用通过接枝聚(苯乙烯磺酸钠)(pNaSS)功能化的聚(ε-己内酯)(PCL)薄膜,来递送携带高软骨再生转化生长因子β(TGF-β)序列的重组腺相关病毒(rAAV)载体的潜力,将其作为未来软骨损伤治疗的靶点。使用接枝和未接枝pNaSS的PCL薄膜进行递送时,rAAV在抽吸物中实现了TGF-β的有效过表达,持续长达21天(评估的最长时间点),与未进行载体包被的相应条件相比,接枝薄膜的表达水平更高。接枝和未接枝pNaSS的PCL薄膜产生的rAAV介导的TGF-β显著触发了样品中的生物学活性和软骨生成过程(蛋白聚糖和II型胶原蛋白沉积以及细胞增殖),同时相对于其他条件含有过早的矿化和肥大现象,总体上接枝pNaSS的薄膜具有更优的效果。这些观察结果表明,PCL薄膜辅助的rAAV TGF-β基因转移作为一种方便的现成技术,在未来改善软骨修复的方法中具有增强患者骨髓修复潜力的潜力。