注射植入物治疗声带瘢痕的未来结果和当前局限性。

IF 5.4
Nour Awad, Denzel Ryan D Cruz, Luigi Melaragno, Sapir Pinhas, Peter J Larson, Gregory R Dion
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引用次数: 0

摘要

声带瘢痕形成是一个重大的挑战。它的特征是由于固有层固有细胞外基质(ECM)的破坏和柔韧性的丧失而导致声带功能的长期和经常不可逆转的损害。目前的治疗在很大程度上仍然是姑息性的,旨在改善声门关闭,而不是恢复正常的组织生物力学。随着对伤口愈合途径和瘢痕形成的纤维化机制的深入研究,注射疗法正在成为调节愈合和恢复振动功能的方法。涵盖领域:本综述概述了声带瘢痕的病理生理学,并评估了旨在恢复组织结构和功能的新兴注射策略。这些包括基于生物材料的植入物、抗纤维化和促再生生物制剂、干细胞疗法和先进的药物输送系统。翻译方面的挑战包括解剖学限制、递送精度、动物模型、免疫相容性、降解动力学以及缺乏标准化的结果测量。专家意见:该综述强调了正在进行的注射植入物治疗声带瘢痕的研究,该研究支持生物力学特性和调节局部组织修复。然而,需要进一步的高级和长期研究,包括临床试验,以充分阐明其安全性,有效性和毒性。此外,它们在制药生产中的可扩展性和可重复性必须经过严格验证,以支持临床翻译。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Future outcomes and current limitations of injectable implants for vocal fold scarring.

Introduction: Vocal fold (VF) scarring poses a significant challenge. It is characterized by prolonged and often irreversible impairment of vocal function due to loss of pliability and disruption of the lamina propria's native extracellular matrix. Current treatments remain largely palliative, aiming to improve glottic closure rather than restore normal tissue biomechanics. As research deepens into the wound healing pathways and fibrotic mechanisms underlying scar formation, injectable therapies are emerging as approaches to modulate healing and restore vibratory function.

Areas covered: This review outlines the pathophysiology of VF scarring and evaluates emerging injectable strategies designed to restore tissue architecture and function. These include biomaterial-based implants, antifibrotic and pro-regenerative biologics, stem cell therapies, and advanced drug delivery systems. The translational challenges include anatomical constraints, delivery precision, animal models, immune compatibility, degradation kinetics, and the lack of standardized outcome measures.

Expert opinion: The review highlights the ongoing research on injections of implants for VF scarring that support biomechanical properties and modulate local tissue repair. However, further advanced and long-term studies, including clinical trials, are needed to fully elucidate their safety, efficacy, and toxicity profiles. In addition, their scalability and reproducibility within pharmaceutical manufacturing must be rigorously validated to support clinical translation.

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