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Circulating mesenchymal stem cells, stromal derived factor (SDF)-1 and IP-10 levels increased in clinically active multiple sclerosis patients but not in clinically stable patients treated with beta interferon.循环间充质干细胞、基质衍生因子 (SDF)-1 和 IP-10 水平在临床上活跃的多发性硬化症患者中升高,但在接受β干扰素治疗的临床上稳定的患者中没有升高。
Mult Scler Relat Disord. 2019 Oct;35:233-238. doi: 10.1016/j.msard.2019.08.013. Epub 2019 Aug 12.
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Immunosuppressive Effect of Exosomes from Mesenchymal Stromal Cells in Defined Medium on Experimental Colitis.间充质基质细胞在特定培养基中分泌的外泌体对实验性结肠炎的免疫抑制作用
Int J Stem Cells. 2019 Nov 30;12(3):440-448. doi: 10.15283/ijsc18139.
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Exosomes derived from mesenchymal stem cells attenuate inflammation and demyelination of the central nervous system in EAE rats by regulating the polarization of microglia.骨髓间充质干细胞来源的外泌体通过调节小胶质细胞极化来减轻 EAE 大鼠中枢神经系统的炎症和脱髓鞘。
Int Immunopharmacol. 2019 Feb;67:268-280. doi: 10.1016/j.intimp.2018.12.001. Epub 2018 Dec 17.
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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.
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Therapeutic Potential of Mesenchymal Cell-Derived miRNA-150-5p-Expressing Exosomes in Rheumatoid Arthritis Mediated by the Modulation of MMP14 and VEGF.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.
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AMSC-derived exosomes alleviate lipopolysaccharide/d-galactosamine-induced acute liver failure by miR-17-mediated reduction of TXNIP/NLRP3 inflammasome activation in macrophages.AMSC 衍生的外泌体通过 miR-17 介导的 TXNIP/NLRP3 炎性小体激活减少减轻脂多糖/半乳糖胺诱导的急性肝衰竭。
EBioMedicine. 2018 Oct;36:140-150. doi: 10.1016/j.ebiom.2018.08.054. Epub 2018 Sep 6.
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A comprehensive review on the treatment approaches of multiple sclerosis: currently and in the future.多发性硬化症的治疗方法综述:现状与未来。
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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.
10
Mesenchymal Stem Cell-Based Immunomodulation: Properties and Clinical Application.基于间充质干细胞的免疫调节:特性与临床应用
Stem Cells Int. 2018 Jun 14;2018:3057624. doi: 10.1155/2018/3057624. eCollection 2018.

间充质干细胞衍生的外泌体:治疗自身免疫性疾病的一张有前景的王牌。

Mesenchymal Stem Cell-Derived Exosomes: A Promising Therapeutic Ace Card to Address Autoimmune Diseases.

作者信息

Baharlooi Hussein, Azimi Maryam, Salehi Zahra, Izad Maryam

机构信息

Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Immunology Research Center, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran.

出版信息

Int J Stem Cells. 2020 Mar 30;13(1):13-23. doi: 10.15283/ijsc19108.

DOI:10.15283/ijsc19108
PMID:31887849
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7119210/
Abstract

With the development of novel treatments for autoimmune disorders, it has become a popular research focus which mesenchymal stem cells (MSCs) have the capacity to counteract with autoimmune diseases progression. One of the underlying mechanisms behind their activities is the release of extracellular vesicles especially exosomes. MSC-derived exosomes are hypoimmunogenic nanocarriers which contain numerous immunoregulatory factors and similar to other exosomes, are able to pass through boundaries like the blood-brain barrier (BBB). Accumulating evidence provided by animal studies has demonstrated that MSC-derived exosomes, as a novel therapy, can re-induce self-tolerance, without subsequent complications reported for other treatments. Therefore, therapeutic applications of MSC-derived exosomes are contributing to core advances in the field of autoimmune diseases. Here, we briefly describe the biological characteristics of MSC-derived exosomes and review the experimentally verified outcomes for autoimmune disease therapy purposes.

摘要

随着自身免疫性疾病新型治疗方法的发展,间充质干细胞(MSCs)是否有能力对抗自身免疫性疾病进展已成为一个热门研究焦点。其作用背后的潜在机制之一是细胞外囊泡尤其是外泌体的释放。MSC来源的外泌体是低免疫原性的纳米载体,含有众多免疫调节因子,并且与其他外泌体类似,能够穿过血脑屏障(BBB)等边界。动物研究提供的越来越多的证据表明,MSC来源的外泌体作为一种新型疗法,可以重新诱导自身耐受性,且没有报道其他治疗方法会出现的后续并发症。因此,MSC来源的外泌体的治疗应用正在推动自身免疫性疾病领域的核心进展。在此,我们简要描述了MSC来源的外泌体的生物学特性,并综述了用于自身免疫性疾病治疗目的的经实验验证的结果。