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TGF-b: A Fibrotic Factor in Wound Scarring and a Potential Target for Anti- Scarring Gene Therapy

机译:TGF-b:瘢痕形成中的纤维化因子和抗瘢痕形成基因治疗的潜在目标

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摘要

Hypertrophic scar and keloid are common and difficult to treat diseases in plastic surgery. Results of wound healing research over the past decades have demonstrated that transforming growth factor-b (TGF-b) plays an essential role in cutaneous scar formation. In contrast, fetal wounds, which heal without scarring, contain a lower level of TGF-b than adult wounds. How to translate the discovery of basic scientific research into the clinical treatment of wound scarring has become an important issue to both clinicians and basic researchers. The development of gene therapy techniques offers the potential to genetically modify adult wound healing to a healing process similar to fetal wounds, and thus reduces wound scarring. This article intends to review the roles of TGF-b in the formation of wound scarring, the possible strategies of antagonizing wound TGF-b, and our preliminary results of scar gene therapy, which show that wound scarring can be significantly reduced by targeting wound TGF-b.
机译:增生性瘢痕和瘢痕loid是常见的,在整形外科中难以治疗。过去几十年中伤口愈合研究的结果表明,转化生长因子b(TGF-b)在皮肤瘢痕形成中起着至关重要的作用。相反,可以治愈而不会留下疤痕的胎儿伤口所含的TGF-b水平低于成人伤口。如何将基础科学研究的发现转化为伤口疤痕的临床治疗已成为临床医生和基础研究人员的重要课题。基因治疗技术的发展提供了将成人伤口愈合基因改造成类似于胎儿伤口的愈合过程的潜力,从而减少了伤口疤痕。本文旨在回顾TGF-b在伤口疤痕形成中的作用,拮抗伤口TGF-b的可能策略以及我们的疤痕基因治疗的初步结果,这些结果表明,靶向伤口TGF可以显着减少伤口疤痕-b。

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