Literature DB >> 35918892

Macrophages as a therapeutic target to promote diabetic wound healing.

Maryam Sharifiaghdam1, Elnaz Shaabani1, Reza Faridi-Majidi2, Stefaan C De Smedt3, Kevin Braeckmans4, Juan C Fraire5.   

Abstract

It is well‏ ‏established that macrophages are key regulators of wound healing, displaying impressive plasticity and an evolving phenotype, from an aggressive pro-inflammatory or "M1" phenotype to a pro-healing or "M2" phenotype, depending on the wound healing stage, to ensure proper healing. Because dysregulated macrophage responses have been linked to impaired healing of diabetic wounds, macrophages are being considered as a therapeutic target for improved wound healing. In this review, we first discuss the role of macrophages in a normal skin wound healing process and discuss the aberrations that occur in macrophages under diabetic conditions. Next we provide an overview of recent macrophage-based therapeutic approaches, including delivery of ex-vivo-activated macrophages and delivery of pharmacological strategies aimed at eliminating or re-educating local skin macrophages. In particular, we focus on strategies to silence key regulator genes to repolarize wound macrophages to the M2 phenotype, and we provide a discussion of their potential future clinical translation.
Copyright © 2022 The American Society of Gene and Cell Therapy. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  IRF5; M1; M2; drug delivery; inflammation; macrophage; siRNA; wound healing

Mesh:

Year:  2022        PMID: 35918892      PMCID: PMC9482022          DOI: 10.1016/j.ymthe.2022.07.016

Source DB:  PubMed          Journal:  Mol Ther        ISSN: 1525-0016            Impact factor:   12.910


  165 in total

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