Department of Pharmacology and Toxicology, School of Biomedical Sciences; Dunedin, New Zealand.
Department of Chemistry, University of Otago, Dunedin, New Zealand.
Adv Wound Care (New Rochelle). 2021 Nov;10(11):596-622. doi: 10.1089/wound.2020.1183. Epub 2020 Nov 25.
Wound healing involves the phasic production of growth factors (GFs) and cytokines to progress an acute wound to a resolved scar. Dysregulation of these proteins contributes to both wound chronicity and excessive scarring. Direct supplementation of GFs and cytokines for treatment of healing and scarring complications has, however, been disappointing. Failings likely relate to an inability to deliver recombinant proteins at physiologically relevant levels to an environment conducive to healing. Inspired by the extracellular matrix, natural biomaterials have been developed that resemble human skin, and are capable of delivering bioactives. Hybrid biomaterials made using multiple polymers, fabrication methods, and proteins are proving efficacious in animal models of acute and impaired wound healing. For clinical translation, these delivery systems must be tailored for specific wound indications and the correct phase of healing. GFs and cytokines must be delivered in a controlled manner that will target specific healing or scarring impairments. Preclinical assessment in clinically relevant animal models of impaired or excessive healing is critical. Clinical success will likely depend on the GF or cytokine selected, their compatibility with the chosen biomaterial(s), degradation rate of the fabricated system, and the degree of control over release kinetics. Further testing is essential to assess which wound indications are most suited to specific delivery systems and to prove whether they provide superior efficacy over direct protein therapies.
伤口愈合涉及生长因子 (GFs) 和细胞因子的阶段性产生,以将急性伤口进展为已解决的疤痕。这些蛋白质的失调会导致伤口慢性化和过度瘢痕形成。然而,直接补充 GFs 和细胞因子来治疗愈合和瘢痕形成并发症的效果并不理想。失败的原因可能与无法在有利于愈合的环境中以生理相关水平递送达重组蛋白有关。受细胞外基质的启发,已经开发出类似于人类皮肤的天然生物材料,并且能够递送生物活性剂。使用多种聚合物、制造方法和蛋白质制造的混合生物材料在急性和受损伤口愈合的动物模型中被证明是有效的。为了进行临床转化,这些输送系统必须针对特定的伤口指征和正确的愈合阶段进行定制。GFs 和细胞因子必须以受控的方式递送到特定的愈合或瘢痕形成障碍部位。在具有临床相关性的受损或过度愈合的动物模型中进行临床前评估至关重要。临床成功可能取决于所选择的 GF 或细胞因子、它们与所选生物材料的兼容性、所制造系统的降解速率以及对释放动力学的控制程度。进一步的测试对于评估哪些伤口指征最适合特定的输送系统以及证明它们是否比直接蛋白治疗提供更好的疗效至关重要。