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间充质干细胞在哮喘炎症亚型中的新见解。

New insights into mesenchymal stem cells in inflammatory subtypes of asthma.

作者信息

Hou Zheng-Yan, Hao Yu-Qiu, Zhang Lin, Li Wei, Gao Peng

机构信息

Department of Respiratory & Critical Care Medicine, Hospital 2, Jilin University, Changchun, China.

出版信息

Front Immunol. 2025 Aug 26;16:1649597. doi: 10.3389/fimmu.2025.1649597. eCollection 2025.

DOI:10.3389/fimmu.2025.1649597
PMID:40933990
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12417199/
Abstract

Asthma is a heterogeneous disease characterized by chronic airway inflammation, heightened reactivity, and structural remodeling. The responses of different phenotypes to traditional corticosteroid therapy vary significantly, with steroid resistance in low T-helper type 2 asthma remaining an urgent clinical challenge. In recent years, mesenchymal stem cells (MSCs) and their exosomes-mesenchymal stem cell-derived extracellular vesicles (MSC-EVs)-have emerged as promising therapeutic agents due to their potent immunomodulatory properties. In this review, we systematically explain how MSCs and MSC-EVs inhibit airway inflammation in asthma through multi-target immunoregulation, highlight their therapeutic potential in steroid-resistant asthma, and outline the challenges and optimization strategies involved in clinical translation, thereby providing a theoretical foundation for the development of novel therapies.

摘要

哮喘是一种异质性疾病,其特征为慢性气道炎症、高反应性和结构重塑。不同表型对传统皮质类固醇疗法的反应差异显著,低2型辅助性T细胞哮喘中的类固醇抵抗仍然是一项紧迫的临床挑战。近年来,间充质干细胞(MSCs)及其外泌体——间充质干细胞衍生的细胞外囊泡(MSC-EVs)——因其强大的免疫调节特性而成为有前景的治疗剂。在本综述中,我们系统地解释了MSCs和MSC-EVs如何通过多靶点免疫调节抑制哮喘中的气道炎症,强调了它们在类固醇抵抗性哮喘中的治疗潜力,并概述了临床转化中涉及的挑战和优化策略,从而为新型疗法的开发提供理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e135/12417199/fec49d74cb75/fimmu-16-1649597-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e135/12417199/380e1b63df0c/fimmu-16-1649597-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e135/12417199/fec49d74cb75/fimmu-16-1649597-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e135/12417199/380e1b63df0c/fimmu-16-1649597-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e135/12417199/fec49d74cb75/fimmu-16-1649597-g002.jpg

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本文引用的文献

1
Circadian Clock Disruption and Non-type 2 Asthma: A Hypothesis-Driven Perspective on Immune, Epithelial, and Steroid Response.昼夜节律紊乱与非2型哮喘:关于免疫、上皮及类固醇反应的假说驱动观点
Clin Rev Allergy Immunol. 2025 Jul 25;68(1):72. doi: 10.1007/s12016-025-09088-5.
2
Pulmonary fibroblast-derived stem cell factor promotes neutrophilic asthma by augmenting IL-17A production from ILC3s.肺成纤维细胞衍生的干细胞因子通过增加3型固有淋巴细胞产生白细胞介素-17A来促进嗜中性粒细胞性哮喘。
J Clin Invest. 2025 Jul 17;135(16). doi: 10.1172/JCI187372. eCollection 2025 Aug 15.
3
2025 GINA report for asthma.
2025年哮喘全球防治创议报告
Lancet Respir Med. 2025 Jun 26. doi: 10.1016/S2213-2600(25)00242-5.
4
Sputum Cellularity and MRI Ventilation Defects in Severe Asthma.重度哮喘患者的痰液细胞组成与MRI通气缺陷
Chest. 2025 May 20. doi: 10.1016/j.chest.2025.05.013.
5
HGF-DPSCs ameliorate asthma by regulating CCR1 Th2 cells responses in mice pulmonary mucosa.肝细胞生长因子-牙髓干细胞通过调节小鼠肺黏膜中CCR1 Th2细胞反应来改善哮喘。
Cytotherapy. 2025 Jun;27(6):709-722. doi: 10.1016/j.jcyt.2025.02.005. Epub 2025 Feb 24.
6
Migrasomes derived from human umbilical cord mesenchymal stem cells: a new therapeutic agent for ovalbumin-induced asthma in mice.源自人脐带间充质干细胞的迁移小体:一种治疗小鼠卵清蛋白诱导哮喘的新型治疗剂。
Stem Cell Res Ther. 2025 Jan 26;16(1):26. doi: 10.1186/s13287-025-04145-4.
7
Mechanism and application of mesenchymal stem cells and their secreting extracellular vesicles in regulating CD4T cells in immune diseases.间充质干细胞及其分泌的细胞外囊泡在免疫疾病中调节CD4 T细胞的机制与应用
Biophys Rep. 2024 Dec 31;10(6):403-415. doi: 10.52601/bpr.2024.240005.
8
CTSS contributes to airway neutrophilic inflammation in mixed granulocytic asthma.胱天蛋白酶-1在混合粒细胞性哮喘中导致气道嗜中性粒细胞炎症。
Respir Res. 2024 Dec 24;25(1):441. doi: 10.1186/s12931-024-03077-6.
9
Corrigendum to "Exosomes from TNF-α-treated human gingiva-derived MSCs enhance M2 macrophage polarization and inhibit periodontal bone loss" [Acta Biomaterialia 2021, 122, 306-324].《肿瘤坏死因子-α处理的人牙龈间充质干细胞来源的外泌体增强M2巨噬细胞极化并抑制牙周骨丢失》[《生物材料学报》2021年,第122卷,第306 - 324页]的勘误
Acta Biomater. 2025 Jan 1;191:428-429. doi: 10.1016/j.actbio.2024.11.029. Epub 2024 Dec 1.
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Tezepelumab for severe asthma: elevating current practice to recognize epithelial driven profiles.特泽布尔单抗治疗严重哮喘:提升现有实践水平以识别上皮细胞驱动型特征。
Respir Res. 2024 Oct 9;25(1):367. doi: 10.1186/s12931-024-02998-6.