• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于间充质干细胞的自身免疫性疾病治疗:细胞外囊泡的新作用

Mesenchymal stem cell-based therapy for autoimmune diseases: emerging roles of extracellular vesicles.

作者信息

Rad Fariba, Ghorbani Mohammad, Mohammadi Roushandeh Amaneh, Habibi Roudkenar Mehryar

机构信息

Cellular and Molecular Research Center, Yasuj University of Medical Sciences, Yasuj, Iran.

Department of Hematology and Blood Banking, Gonabad University of Medical Sciences, Gonabad, Iran.

出版信息

Mol Biol Rep. 2019 Feb;46(1):1533-1549. doi: 10.1007/s11033-019-04588-y. Epub 2019 Jan 8.

DOI:10.1007/s11033-019-04588-y
PMID:30623280
Abstract

In autoimmune disease body's own immune system knows healthy cells as undesired and foreign cells. Over 80 types of autoimmune diseases have been recognized. Currently, at clinical practice, treatment strategies for autoimmune disorders are based on relieving symptoms and preventing difficulties. In other words, there is no effective and useful therapy up to now. It has been well-known that mesenchymal stem cells (MSCs) possess immunomodulatory effects. This strongly suggests that MSCs might be as a novel modality for treatment of autoimmune diseases. Supporting this notion a few preclinical and clinical studies indicate that MSCs ameliorate autoimmune disorders. Interestingly, it has been found that the beneficial effects of MSCs in autoimmune disorders are not relying only on direct cell-to-cell communication but on their capability to produce a broad range of paracrine factors including growth factors, cytokines and extracellular vehicles (EVs). EVs are multi-signal messengers that play a serious role in intercellular signaling through carrying cargo such as mRNA, miRNA, and proteins. Numerous studies have shown that MSC-derived EVs are able to mimic the effects of the cell of origin on immune cells. In this review, we discuss the current studies dealing with MSC-based therapies in autoimmune diseases and provide a vision and highlight in order to introduce MSC-derived EVs as an alternative and emerging modality for autoimmune disorders.

摘要

在自身免疫性疾病中,机体自身的免疫系统将健康细胞识别为不需要的外来细胞。目前已确认超过80种自身免疫性疾病。当前在临床实践中,自身免疫性疾病的治疗策略基于缓解症状和预防并发症。换句话说,到目前为止尚无有效且有用的治疗方法。众所周知,间充质干细胞(MSCs)具有免疫调节作用。这强烈表明MSCs可能是治疗自身免疫性疾病的一种新方法。一些临床前和临床研究支持了这一观点,表明MSCs可改善自身免疫性疾病。有趣的是,已发现MSCs在自身免疫性疾病中的有益作用不仅依赖于直接的细胞间通讯,还依赖于它们产生多种旁分泌因子的能力,这些因子包括生长因子、细胞因子和细胞外囊泡(EVs)。EVs是多信号信使,通过携带mRNA、miRNA和蛋白质等货物在细胞间信号传导中发挥重要作用。大量研究表明,源自MSCs的EVs能够模拟起源细胞对免疫细胞的作用。在本综述中,我们讨论了目前关于基于MSCs治疗自身免疫性疾病的研究,并提供了展望和重点内容,以便将源自MSCs的EVs作为自身免疫性疾病的一种替代且新兴的治疗方法进行介绍。

相似文献

1
Mesenchymal stem cell-based therapy for autoimmune diseases: emerging roles of extracellular vesicles.基于间充质干细胞的自身免疫性疾病治疗:细胞外囊泡的新作用
Mol Biol Rep. 2019 Feb;46(1):1533-1549. doi: 10.1007/s11033-019-04588-y. Epub 2019 Jan 8.
2
Therapeutic potential of mesenchymal stem cell-derived extracellular vesicles as novel cell-free therapy for treatment of autoimmune disorders.间充质干细胞衍生的细胞外囊泡作为治疗自身免疫性疾病的新型无细胞疗法的治疗潜力。
Exp Mol Pathol. 2021 Feb;118:104566. doi: 10.1016/j.yexmp.2020.104566. Epub 2020 Nov 6.
3
The developing role of extracellular vesicles in autoimmune diseases: special attention to mesenchymal stem cell-derived extracellular vesicles.细胞外囊泡在自身免疫性疾病中的发展作用:特别关注间充质干细胞衍生的细胞外囊泡。
Int Immunopharmacol. 2023 Sep;122:110531. doi: 10.1016/j.intimp.2023.110531. Epub 2023 Jul 10.
4
Therapeutic Implications of Mesenchymal Stromal Cells and Their Extracellular Vesicles in Autoimmune Diseases: From Biology to Clinical Applications.间充质基质细胞及其细胞外囊泡在自身免疫性疾病中的治疗意义:从生物学到临床应用。
Int J Mol Sci. 2021 Sep 20;22(18):10132. doi: 10.3390/ijms221810132.
5
Therapeutic prospects of MicroRNAs carried by mesenchymal stem cells-derived extracellular vesicles in autoimmune diseases.间充质干细胞衍生的细胞外囊泡携带的 microRNAs 在自身免疫性疾病中的治疗前景。
Life Sci. 2021 Jul 15;277:119458. doi: 10.1016/j.lfs.2021.119458. Epub 2021 Apr 6.
6
Immunomodulatory Effects of Mesenchymal Stem Cells and Mesenchymal Stem Cell-Derived Extracellular Vesicles in Rheumatoid Arthritis.间充质干细胞及其衍生的细胞外囊泡在类风湿关节炎中的免疫调节作用。
Front Immunol. 2020 Aug 20;11:1912. doi: 10.3389/fimmu.2020.01912. eCollection 2020.
7
Taking advantage of the potential of mesenchymal stromal cells in liver regeneration: Cells and extracellular vesicles as therapeutic strategies.利用间充质基质细胞在肝脏再生中的潜力:细胞和细胞外囊泡作为治疗策略。
World J Gastroenterol. 2018 Jun 21;24(23):2427-2440. doi: 10.3748/wjg.v24.i23.2427.
8
Functional proteins of mesenchymal stem cell-derived extracellular vesicles.间充质干细胞衍生细胞外囊泡的功能蛋白。
Stem Cell Res Ther. 2019 Nov 28;10(1):359. doi: 10.1186/s13287-019-1484-6.
9
Mesenchymal stem cell-derived extracellular vesicles attenuate pulmonary vascular permeability and lung injury induced by hemorrhagic shock and trauma.间充质干细胞衍生的细胞外囊泡可减轻失血性休克和创伤引起的肺血管通透性和肺损伤。
J Trauma Acute Care Surg. 2018 Feb;84(2):245-256. doi: 10.1097/TA.0000000000001744.
10
Unlocking the Potential of Extracellular Vesicles as the Next Generation Therapy: Challenges and Opportunities.解锁细胞外囊泡作为下一代治疗方法的潜力:挑战与机遇。
Tissue Eng Regen Med. 2024 Jun;21(4):513-527. doi: 10.1007/s13770-024-00634-4. Epub 2024 Apr 10.

引用本文的文献

1
Therapeutic Potential of Umbilical Cord MSC-Derived Exosomes in a Severe Dry Eye Rat Model: Enhancing Corneal Protection and Modulating Inflammation.脐带间充质干细胞衍生外泌体在严重干眼大鼠模型中的治疗潜力:增强角膜保护和调节炎症
Biomedicines. 2025 May 11;13(5):1174. doi: 10.3390/biomedicines13051174.
2
Immune-regulating extracellular vesicles: a new frontier in autoimmune disease therapy.免疫调节细胞外囊泡:自身免疫性疾病治疗的新前沿。
Essays Biochem. 2025 May 13. doi: 10.1042/EBC20253016.
3
Current advancements in cellular immunotherapy for autoimmune disease.

本文引用的文献

1
Exosome mediated phenotypic changes in lung cancer pathophysiology.外泌体介导肺癌病理生理学中的表型变化。
Transl Cancer Res. 2017 Aug;6(Suppl 6):S1040-S1042. doi: 10.21037/tcr.2017.07.09.
2
Therapeutic potential of extracellular vesicles derived from human mesenchymal stem cells in a model of progressive multiple sclerosis.人骨髓间充质干细胞来源的细胞外囊泡在进展型多发性硬化模型中的治疗潜力。
PLoS One. 2018 Sep 19;13(9):e0202590. doi: 10.1371/journal.pone.0202590. eCollection 2018.
3
Therapeutic Potential of Mesenchymal Cell-Derived miRNA-150-5p-Expressing Exosomes in Rheumatoid Arthritis Mediated by the Modulation of MMP14 and VEGF.
自身免疫性疾病细胞免疫疗法的当前进展。
Semin Immunopathol. 2025 Jan 16;47(1):7. doi: 10.1007/s00281-024-01034-5.
4
Nanomedicine regulating PSC-mediated intercellular crosstalk: Mechanisms and therapeutic strategies.纳米医学调控PSC介导的细胞间串扰:机制与治疗策略
Acta Pharm Sin B. 2024 Nov;14(11):4756-4775. doi: 10.1016/j.apsb.2024.07.007. Epub 2024 Jul 10.
5
Anti-necroptotic effects of human Wharton's jelly-derived mesenchymal stem cells in skeletal muscle cell death model via secretion of GRO-α.人脐带华通氏胶间充质干细胞通过分泌GRO-α对骨骼肌细胞死亡模型的抗坏死性凋亡作用
PLoS One. 2024 Dec 2;19(12):e0313693. doi: 10.1371/journal.pone.0313693. eCollection 2024.
6
Understanding molecular characteristics of extracellular vesicles derived from different types of mesenchymal stem cells for therapeutic translation.了解源自不同类型间充质干细胞的细胞外囊泡的分子特征以用于治疗转化。
Extracell Vesicle. 2024 Jun;3. doi: 10.1016/j.vesic.2024.100034. Epub 2024 Mar 2.
7
Controversies regarding transplantation of mesenchymal stem cells.间充质干细胞移植的争议
World J Transplant. 2024 Jun 18;14(2):90554. doi: 10.5500/wjt.v14.i2.90554.
8
Mesenchymal stromal cells protect tissues from Th1 immune responses via IL-11 secretion.间质基质细胞通过分泌白细胞介素-11 来保护组织免受 Th1 免疫应答的影响。
FASEB J. 2024 May 31;38(10):e23683. doi: 10.1096/fj.202400078R.
9
Peptoid-Cross-Linked Hydrogel Stiffness Modulates Human Mesenchymal Stromal Cell Immunoregulatory Potential in the Presence of Interferon-Gamma.在干扰素-γ存在的情况下,类肽交联水凝胶的硬度调节人间充质基质细胞的免疫调节潜能。
Macromol Biosci. 2024 Jul;24(7):e2400111. doi: 10.1002/mabi.202400111. Epub 2024 Apr 18.
10
hUC-MSCs-derived MFGE8 ameliorates locomotor dysfunction via inhibition of ITGB3/ NF-κB signaling in an NMO mouse model.在视神经脊髓炎小鼠模型中,人脐带间充质干细胞来源的乳脂肪球表皮生长因子8通过抑制整合素β3/核因子κB信号通路改善运动功能障碍。
NPJ Regen Med. 2024 Jan 20;9(1):4. doi: 10.1038/s41536-024-00349-z.
间充质细胞衍生 miRNA-150-5p 表达外泌体通过调节 MMP14 和 VEGF 在类风湿关节炎中的治疗潜力。
J Immunol. 2018 Oct 15;201(8):2472-2482. doi: 10.4049/jimmunol.1800304. Epub 2018 Sep 17.
4
Mesenchymal stem cells-derived IL-6 activates AMPK/mTOR signaling to inhibit the proliferation of reactive astrocytes induced by hypoxic-ischemic brain damage.间质干细胞衍生的白细胞介素 6 通过激活 AMPK/mTOR 信号通路抑制低氧缺血性脑损伤诱导的反应性星形胶质细胞的增殖。
Exp Neurol. 2019 Jan;311:15-32. doi: 10.1016/j.expneurol.2018.09.006. Epub 2018 Sep 10.
5
Critical Role of Tumor Necrosis Factor Signaling in Mesenchymal Stem Cell-Based Therapy for Autoimmune and Inflammatory Diseases.肿瘤坏死因子信号通路在基于间充质干细胞的自身免疫性和炎性疾病治疗中的关键作用
Front Immunol. 2018 Jul 20;9:1658. doi: 10.3389/fimmu.2018.01658. eCollection 2018.
6
Immunomodulatory effects of mesenchymal stem cell-derived exosomes on experimental type-1 autoimmune diabetes.间充质干细胞来源的外泌体对实验性 1 型自身免疫性糖尿病的免疫调节作用。
J Cell Biochem. 2018 Nov;119(11):9433-9443. doi: 10.1002/jcb.27260. Epub 2018 Aug 3.
7
TGF-β and mesenchymal stromal cells in regenerative medicine, autoimmunity and cancer.转化生长因子-β与间充质基质细胞在再生医学、自身免疫和癌症中的作用。
Cytokine Growth Factor Rev. 2018 Oct;43:25-37. doi: 10.1016/j.cytogfr.2018.06.002. Epub 2018 Jun 13.
8
Contribution of the macrophage migration inhibitory factor superfamily of cytokines in the pathogenesis of preclinical and human multiple sclerosis: In silico and in vivo evidences.细胞因子巨噬细胞移动抑制因子超家族在临床前和人类多发性硬化症发病机制中的作用:计算机模拟和体内证据。
J Neuroimmunol. 2018 Sep 15;322:46-56. doi: 10.1016/j.jneuroim.2018.06.009. Epub 2018 Jun 15.
9
Inhibitory Effects of iPSC-MSCs and Their Extracellular Vesicles on the Onset of Sialadenitis in a Mouse Model of Sjögren's Syndrome.诱导多能干细胞来源的间充质干细胞及其细胞外囊泡对干燥综合征小鼠模型涎腺炎发病的抑制作用
Stem Cells Int. 2018 Mar 15;2018:2092315. doi: 10.1155/2018/2092315. eCollection 2018.
10
Mesenchymal Stem Cells on Horizon: A New Arsenal of Therapeutic Agents.间充质干细胞:治疗新武器。
Stem Cell Rev Rep. 2018 Aug;14(4):484-499. doi: 10.1007/s12015-018-9817-x.