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间充质基质细胞治疗移植物抗宿主病。

Mesenchymal Stromal Cells for the Treatment of Graft Versus Host Disease.

机构信息

Cynata Therapeutics Limited, Cremorne, VIC, Australia.

Department of Cell and Molecular Therapies, Royal Prince Alfred Hospital, Sydney, NSW, Australia.

出版信息

Front Immunol. 2021 Oct 26;12:761616. doi: 10.3389/fimmu.2021.761616. eCollection 2021.

Abstract

Graft versus host disease (GvHD) is a life-threating complication of allogeneic hematopoietic stem cell transplantation, which is initially treated with high dose corticosteroids. Approximately 50% of acute GvHD cases are resistant to steroid treatment, and two-year mortality rates in those steroid-resistant patients exceed 80%. Chronic GvHD necessitates prolonged corticosteroid use, which is typically associated with limited efficacy and troublesome adverse effects. No agent has yet been established as an optimal second line therapy for either acute or chronic GvHD, but mesenchymal stromal cells (MSCs) have shown substantial promise. MSCs promote an immunosuppressive and immunoregulatory environment multifactorial mechanisms, including: secretion of proteins/peptides/hormones; transfer of mitochondria; and transfer of exosomes or microvesicles containing RNA and other molecules. A large number of clinical studies have investigated MSCs from various sources as a treatment for acute and/or chronic GvHD. MSCs are generally safe and well tolerated, and most clinical studies have generated encouraging efficacy results, but response rates have varied. Confounding factors include variability in MSC donor types, production methodology and dose regimens, as well as variations in study design. It is well-established that extensive culture expansion of primary donor-derived MSCs leads to marked changes in functionality, and that there is a high level of inter-donor variability in MSC properties. However, recent manufacturing innovations may be capable of overcoming these problems. Further adequately powered prospective studies are required to confirm efficacy and establish the place of MSC therapy in the treatment of this condition.

摘要

移植物抗宿主病(GvHD)是异基因造血干细胞移植的一种危及生命的并发症,最初用大剂量皮质类固醇治疗。大约 50%的急性 GvHD 病例对类固醇治疗有抗药性,而那些对类固醇耐药的患者两年死亡率超过 80%。慢性 GvHD 需要长期使用皮质类固醇,通常疗效有限,且不良反应麻烦。目前还没有一种药物被确立为急性或慢性 GvHD 的最佳二线治疗药物,但间充质基质细胞(MSCs)显示出很大的希望。MSCs 通过多种机制促进免疫抑制和免疫调节环境,包括:分泌蛋白质/肽/激素;转移线粒体;以及含有 RNA 和其他分子的外泌体或微泡的转移。大量的临床研究已经研究了来自不同来源的 MSCs 作为治疗急性和/或慢性 GvHD 的方法。MSCs 通常是安全且耐受良好的,大多数临床研究都产生了令人鼓舞的疗效结果,但反应率有所不同。混杂因素包括 MSC 供体类型、生产方法和剂量方案的可变性,以及研究设计的变化。大量研究证实,原代供体来源的 MSCs 的广泛培养扩增会导致功能显著改变,并且 MSC 特性在供体之间存在高度变异性。然而,最近的制造创新可能能够克服这些问题。需要进一步进行足够数量的前瞻性研究,以确认疗效,并确定 MSC 治疗在这种疾病治疗中的地位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c50/8577186/09bd2972a995/fimmu-12-761616-g001.jpg

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