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基于细胞的 RDEB 治疗:它是如何工作的?

Cell-based therapy for RDEB: how does it work?

机构信息

Department of Dermatology and Cutaneous Biology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

J Invest Dermatol. 2011 Aug;131(8):1597-9. doi: 10.1038/jid.2011.125.

Abstract

No effective or specific treatment is currently available for recessive dystrophic epidermolysis bullosa (RDEB), a severe heritable blistering disorder caused by mutations in the type VII collagen gene (COL7A1). Recent studies have suggested that delivery of allogeneic fibroblasts to the skin of patients with RDEB may be beneficial in improving skin adhesion and increasing type VII collagen deposition at the dermal-epidermal junction. In this issue, Nagy et al. explore mechanisms of fibroblast therapy in a patient with RDEB displaying reduced type VII collagen protein expression at the dermal-epidermal junction. The results suggest that allogeneic fibroblast injection elicits expression of cytokines, including heparin binding-EGF-like growth factor (HB-EGF), that upregulate the expression of a patient-specific COL7A1 allele. Thus, fibroblast therapy may provide a novel way to improve skin therapy in a select subgroup of patients with this currently intractable disease.

摘要

目前,尚无有效的特异性治疗方法可用于隐性营养不良型大疱性表皮松解症(RDEB),这是一种严重的遗传性水疱性疾病,由 VII 型胶原基因(COL7A1)突变引起。最近的研究表明,将同种异体成纤维细胞递送至 RDEB 患者的皮肤中可能有益于改善皮肤黏附并增加真皮-表皮交界处的 VII 型胶原沉积。在本期中,Nagy 等人研究了在一个 RDEB 患者中,成纤维细胞治疗的机制,该患者在真皮-表皮交界处显示 VII 型胶原蛋白表达减少。结果表明,同种异体成纤维细胞注射可引发细胞因子的表达,包括肝素结合表皮生长因子样生长因子(HB-EGF),从而上调患者特异性 COL7A1 等位基因的表达。因此,成纤维细胞疗法可能为治疗目前难以治愈的疾病的特定亚组患者提供一种新的改善皮肤治疗的方法。

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