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巨噬细胞免疫调节在糖尿病足溃疡愈合中的新视野

New Horizons of Macrophage Immunomodulation in the Healing of Diabetic Foot Ulcers.

作者信息

Lin Ching-Wen, Hung Chien-Min, Chen Wan-Jiun, Chen Jui-Ching, Huang Wen-Yen, Lu Chia-Sing, Kuo Ming-Liang, Chen Shyi-Gen

机构信息

Oneness Biotech Co., Ltd., Taipei 106, Taiwan.

Microbio Co., Ltd., Taipei 115, Taiwan.

出版信息

Pharmaceutics. 2022 Sep 27;14(10):2065. doi: 10.3390/pharmaceutics14102065.

Abstract

Diabetic foot ulcers (DFUs) are one of the most costly and troublesome complications of diabetes mellitus. The wound chronicity of DFUs remains the main challenge in the current and future treatment of this condition. Persistent inflammation results in chronic wounds characterized by dysregulation of immune cells, such as M1 macrophages, and impairs the polarization of M2 macrophages and the subsequent healing process of DFUs. The interactive regulation of M1 and M2 macrophages during DFU healing is critical and seems manageable. This review details how cytokines and signalling pathways are co-ordinately regulated to control the functions of M1 and M2 macrophages in normal wound repair. DFUs are defective in the M1-to-M2 transition, which halts the whole wound-healing machinery. Many pre-clinical and clinical innovative approaches, including the application of topical insulin, CCL chemokines, micro RNAs, stem cells, stem-cell-derived exosomes, skin substitutes, antioxidants, and the most recent Phase III-approved ON101 topical cream, have been shown to modulate the activity of M1 and M2 macrophages in DFUs. ON101, the newest clinically approved product in this setting, is designed specifically to down-regulate M1 macrophages and further modulate the wound microenvironment to favour M2 emergence and expansion. Finally, the recent evolution of macrophage modulation therapies and techniques will improve the effectiveness of the treatment of diverse DFUs.

摘要

糖尿病足溃疡(DFUs)是糖尿病最昂贵且麻烦的并发症之一。DFUs的伤口慢性化仍是当前及未来治疗该病的主要挑战。持续的炎症导致以免疫细胞(如M1巨噬细胞)失调为特征的慢性伤口,并损害M2巨噬细胞的极化以及随后DFUs的愈合过程。DFU愈合过程中M1和M2巨噬细胞的相互调节至关重要且似乎是可控的。本综述详细阐述了细胞因子和信号通路如何协同调节,以控制正常伤口修复中M1和M2巨噬细胞的功能。DFUs在从M1向M2的转变过程中存在缺陷,这使整个伤口愈合机制停滞。许多临床前和临床创新方法,包括局部应用胰岛素、CCL趋化因子、微小RNA、干细胞、干细胞衍生的外泌体、皮肤替代物、抗氧化剂,以及最近III期批准的ON101外用乳膏,已被证明可调节DFUs中M1和M2巨噬细胞的活性。ON101是该领域最新获得临床批准的产品,专门设计用于下调M1巨噬细胞,并进一步调节伤口微环境,以促进M2巨噬细胞的出现和扩增。最后,巨噬细胞调节疗法和技术的最新进展将提高不同类型DFUs的治疗效果。

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