De Rosa Laura, Enzo Elena, Zardi Giulia, Bodemer Christine, Magnoni Cristina, Schneider Holm, De Luca Michele
Holostem Terapie Avanzate, s.r.l, Modena, Italy.
Centre for Regenerative Medicine "Stefano Ferrari", University of Modena and Reggio Emilia, Modena, Italy.
Front Genet. 2021 Sep 1;12:705019. doi: 10.3389/fgene.2021.705019. eCollection 2021.
Epidermolysis bullosa (EB) is a group of devastating genetic diseases characterized by skin and mucosal fragility and formation of blisters, which develop either spontaneously or in response to minor mechanical trauma. There is no definitive therapy for any form of EB. Intermediate junctional EB (JEB) caused by mutations in the gene has been the first genetic skin disease successfully tackled by gene therapy. Here, we present a multicenter, open-label, uncontrolled phase II/III study that aims at confirming the efficacy of Hologene 5, a graft consisting of cultured transgenic keratinocytes and epidermal stem cells and meant to combine cell and gene therapy for the treatment of -related JEB. Autologous clonogenic keratinocytes will be isolated from patients' skin biopsies, genetically corrected with a gamma-retroviral vector (γRV) carrying the full-length human cDNA and plated onto a fibrin support (144cm). The transgenic epidermis will be transplanted onto surgically prepared selected skin areas of at least six JEB patients (four pediatric and two adults). Evaluation of clinical efficacy will include, as primary endpoint, a combination of clinical parameters, such as percentage of re-epithelialization, cellular, molecular, and functional parameters, mechanical stress tests, and patient-reported outcome (PRO), up to 12months after transplantation. Safety and further efficacy endpoints will also be assessed during the clinical trial and for additional 15years in an interventional non-pharmacological follow-up study. If successful, this clinical trial would provide a therapeutic option for skin lesions of JEB patients with mutations and pave the way to a combined cell and gene therapy platform tackling other forms of EB and different genodermatoses. Clinical Trial Registration: EudraCT Number: 2018-000261-36.
大疱性表皮松解症(EB)是一组严重的遗传性疾病,其特征为皮肤和黏膜脆弱以及水疱形成,水疱可自发出现或因轻微机械创伤而产生。目前尚无针对任何形式EB的确切治疗方法。由该基因突变引起的中间型交界性EB(JEB)是首个通过基因治疗成功攻克的遗传性皮肤病。在此,我们开展了一项多中心、开放标签、非对照的II/III期研究,旨在确认Hologene 5的疗效,Hologene 5是一种由培养的转基因角质形成细胞和表皮干细胞组成的移植物,旨在将细胞治疗和基因治疗相结合,用于治疗与相关的JEB。将从患者的皮肤活检样本中分离出自体克隆性角质形成细胞,用携带全长人cDNA的γ-逆转录病毒载体(γRV)进行基因校正,然后接种到纤维蛋白支架(144平方厘米)上。将转基因表皮移植到至少六名JEB患者(四名儿童和两名成人)经手术准备的选定皮肤区域。临床疗效评估将包括,作为主要终点,一系列临床参数的组合,如再上皮化百分比、细胞、分子和功能参数、机械应力测试以及患者报告结局(PRO),直至移植后12个月。在临床试验期间以及在一项介入性非药物随访研究中额外的15年里,还将评估安全性和其他疗效终点。如果成功,这项临床试验将为携带突变的JEB患者的皮肤病变提供一种治疗选择,并为攻克其他形式的EB和不同遗传性皮肤病的细胞和基因治疗联合平台铺平道路。临床试验注册号:欧洲临床试验数据库编号:2018-000261-36。