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Mesenchymal stem cell derived extracellular vesicles: promising immunomodulators against autoimmune, autoinflammatory disorders and SARS-CoV-2 infection

机译:间充质干细胞衍生的细胞外囊泡:有前途免疫调节剂免疫调节剂免疫调节剂,自身炎症性疾病和SARS-COV-2感染

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Discovery of novel and broad-acting immunomodulators is of critical importance for the prevention and treatment of disorders occurring due to overexuberant immune responseincluding SARS-CoV-2 triggered cytokine storm leading to lung pathology and mortality during the ongoing viral pandemic. Mesenchymal stem/stromal cells (MSCs), highly regarded for their regenerative capacities, also possessesremarkable immunoregulatory functions affecting all types of innate and adaptive immune cells. Owing to that, MSCs have been heavily investigated in clinic for the treatment of autoimmune and inflammatory diseases along with transplant rejection. Extensive research in the last decaderevealed that MSCs carry out most of their functions through paracrine factors which are soluble mediators and extracellular vesicles (EVs). EVs, including exosomes and microvesicles, are an efficient way of intercellular communication due to their unique ability to carry biological messages such as transcription factors, growth factors, cytokines, mRNAs and miRNAs over long distances. EVs originate through direct budding of the cell membrane or the endosomal secretion pathway and they consist of the cytosolic and membrane components of their parent cell. Therefore, they are able to mimic the characteristics of the parent cell, affecting the target cells upon binding or internalization. EVs secreted by MSCs are emerging as a cell-free alternative to MSC-based therapies. MSC EVs are being tested in preclinical and clinical settings where they exhibit exceptional immunosuppressivecapacity. They regulate the migration, proliferation, activation and polarization of various immune cells, promoting a tolerogenic immune response while inhibiting inflammatory response. Being as effective immunomodulators as their parent cells, MSC EVs are also preferable over MSC-based therapies due to their lower risk of immunogenicity, tumorigenicity and overall superior safety. In this review, we present the outcomes of preclinical and clinical studies utilizing MSC EVs as therapeutic agents for the treatment of a wide variety of immunological disorders.
机译:新型和广泛的免疫调节剂的发现对于预防和治疗因过度膨胀的免疫性而导致的SARS-COV-2引发的细胞因子风暴的预防和治疗导致肺病毒流行病中的肺病和死亡率的疾病。间充质茎/基质细胞(MSCs),高度重视其再生能力,也具有影响所有类型的先天性和适应性免疫细胞的令人放大的免疫调节功能。由此,MSCs在临床上被严重研究用于治疗自身免疫和炎症性疾病以及移植排斥。在最后的Decadereveal中进行广泛的研究,MSCS通过帕拉卡碱因子进行大部分功能,该剖腹症因素是可溶的介质和细胞外囊泡(EVS)。 EVS(包括外泌体和微铅)是一种有效的间细胞间通信的方式,因为它们具有在长距离长距离的转录因子,生长因子,细胞因子,MRNA和MIRNA等生物信息的独特能力。 EVS通过细胞膜或内体分泌途径的直接萌芽,并且它们由其亲本细胞的细胞溶质和膜组分组成。因此,它们能够模拟亲本细胞的特性,在结合或内化时影响靶细胞。 MSCs分泌的EVS被涌现为对基于MSC的疗法的无电池替代品。 MSC EVS正在在临床前和临床环境中进行测试,其中它们表现出特殊的免疫抑制性能。它们调节各种免疫细胞的迁移,增殖,激活和极化,同时抑制炎症反应的同时促进耐受性免疫应答。作为其亲本细胞的有效免疫调节剂,由于其较低的免疫原性,致瘤性和总体安全性的安全性,MSC EVS也优于基于MSC的疗法。在本文中,我们介绍了利用MSC EVS作为治疗剂的临床前和临床研究的结果,用于治疗各种免疫障碍。

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