生物类似药基因治疗:Secukinumab基因治疗的研究评估

A. Fallah, H. Estiri, Elizabeth L. Parrish, Mansoureh Soleimani, S. Zeinali, A. Zadeh-Vakili
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引用次数: 1

摘要

肿瘤坏死因子-α (TNF-α)、检查点抑制剂和白细胞介素-17 (IL-17)是炎症和自身免疫性疾病的关键靶点。单克隆抗体(mab)在慢性疾病的治疗中具有成功的组合。随着干细胞和基因治疗技术的进步,有希望用一种更直接、更经济的方法在患者细胞内取代生物反应器中昂贵的单克隆抗体生产。在这篇论文中,我们研究了一项关于secukinumab基因治疗的研究评估结果。材料与方法在慢病毒载体上克隆了secukinumab抗体重链和轻链的DNA序列。分离并鉴定了人绒毛膜绒毛间充质干细胞(CMSCs)。经过慢病毒包装和滴定后,一部分重组病毒用于CMSCs的转导,另一部分用于全身基因治疗。将工程干细胞和重组病毒分别应用于不同组大鼠模型的离体和体内基因治疗。以获批的secukinumab为标准参比,采用定量实时聚合酶链反应(qRT-PCR)、western blot、ELISA等方法确认secukinumab在体外和体内的表达。结果细胞分化实验和标准生物标志物的流式细胞术证实了骨髓间充质干细胞的多能性。Western blot和qRT-PCR在mRNA和蛋白水平上证实了体外secukinumab基因的表达。ELISA检测治疗大鼠模型的血清,证实单抗在体内和体外基因治疗中均过表达。在本研究中,开发了一种慢病毒介导的体外和体内基因治疗方法,为大鼠模型提供中等剂量的secukinumab。生物仿制药基因治疗是治疗自身免疫性疾病、癌症和其他慢性疾病的一种有吸引力的方法。
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Biosimilar Gene Therapy: Investigational Assessment of Secukinumab Gene Therapy
Objective Tumor necrosis factor-alpha (TNF-α), checkpoint inhibitors, and interleukin-17 (IL-17) are critical targets in inflammation and autoimmune diseases. Monoclonal antibodies (mAbs) have a successful portfolio in the treatment of chronic diseases. With the current progress in stem cells and gene therapy technologies, there is the promise of replacing costly mAbs production in bioreactors with a more direct and cost-effective production method inside the patient’s cells. In this paper we examine the results of an investigational assessment of secukinumab gene therapy. Materials and Methods In this experimental study, the DNA sequence of the heavy and light chains of secukinumab antibodies were cloned in a lentiviral vector. Human chorionic villous mesenchymal stem cells (CMSCs) were isolated and characterized. After lentiviral packaging and titration, part of the recombinant viruses was used for transduction of the CMSCs and the other part were applied for systemic gene therapy. The engineered stem cells and recombinant viruses were applied for ex vivo and in vivo gene therapy, respectively, in different groups of rat models. In vitro and in vivo secukinumab expression was confirmed with quantitative real-time polymerase chain reaction (qRT-PCR), western blot, and ELISA by considering the approved secukinumab as the standard reference. Results Cell differentiation assays and flow cytometry of standard biomarkers confirmed the multipotency of the CMSCs. Western blot and qRT-PCR confirmed in vitro gene expression of secukinumab at both the mRNA and protein level. ELISA testing of serum from treated rat models confirmed mAb overexpression for both in vivo and ex vivo gene therapies. Conclusion In this study, a lentiviral-mediated ex vivo and in vivo gene therapy was developed to provide a moderate dose of secukinumab in rat models. Biosimilar gene therapy is an attractive approach for the treatment of autoimmune disorders, cancers and other chronic diseases.
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