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壳聚糖的免疫调节作用:对免疫细胞及信号通路作用机制的见解

Chitosan immunomodulation: insights into mechanisms of action on immune cells and signaling pathways.

作者信息

Ghattas Majed, Dwivedi Garima, Chevrier Anik, Horn-Bourque Delano, Alameh Mohamad-Gabriel, Lavertu Marc

机构信息

Department of Chemical Engineering, Polytechnique Montreal Montreal QC Canada

Institute of Biomedical Engineering, Polytechnique Montreal Montreal QC Canada.

出版信息

RSC Adv. 2025 Jan 10;15(2):896-909. doi: 10.1039/d4ra08406c. eCollection 2025 Jan 9.

Abstract

Chitosan, a biodegradable and biocompatible natural polymer composed of β-(1-4)-linked -acetyl glucosamine (GlcNAc) and d-glucosamine (GlcN) and derived from crustacean shells, has been widely studied for various biomedical applications, including drug delivery, cartilage repair, wound healing, and tissue engineering, because of its unique physicochemical properties. One of the most promising areas of research is the investigation of the immunomodulatory properties of chitosan, since the biopolymer has been shown to modulate the maturation, activation, cytokine production, and polarization of dendritic cells and macrophages, two key immune cells involved in the initiation and regulation of innate and adaptive immune responses, leading to enhanced immune responses. Several signaling pathways, including the cGAS-STING, STAT-1, and NLRP3 inflammasomes, are involved in chitosan-induced immunomodulation. This review provides a comprehensive overview of the current understanding of the immunomodulatory effects of chitosan. This information may facilitate the development of chitosan-based therapies and vaccine adjuvants for various immune-related diseases.

摘要

壳聚糖是一种可生物降解且具有生物相容性的天然聚合物,由β-(1-4)-连接的N-乙酰葡糖胺(GlcNAc)和D-葡糖胺(GlcN)组成,源自甲壳类动物的外壳。由于其独特的物理化学性质,壳聚糖已被广泛研究用于各种生物医学应用,包括药物递送、软骨修复、伤口愈合和组织工程。最有前景的研究领域之一是对壳聚糖免疫调节特性的研究,因为这种生物聚合物已被证明可以调节树突状细胞和巨噬细胞的成熟、激活、细胞因子产生和极化,这两种关键免疫细胞参与先天性和适应性免疫反应的启动和调节,从而增强免疫反应。包括cGAS-STING、STAT-1和NLRP3炎性小体在内的几种信号通路参与了壳聚糖诱导的免疫调节。本综述全面概述了目前对壳聚糖免疫调节作用的理解。这些信息可能有助于开发用于各种免疫相关疾病的基于壳聚糖的疗法和疫苗佐剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c89/11719903/9a4fac59a137/d4ra08406c-f1.jpg

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