[Research advances in mesenchymal stem cell therapy for graft-versus-host disease].

Q3 Medicine
W H Wang, X L Pei, J Y Luo, E L Jiang
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引用次数: 0

Abstract

Graft-versus-host disease (GVHD) remains a severe complication after allogeneic hematopoietic stem cell transplantation, and effective treatment options remain limited, particularly for patients with steroid-refractory GVHD or failure of multiple lines of therapy. Mesenchymal stem cell (MSC) therapy has shown promise for the prevention and treatment of GVHD because of the low immunogenicity and immunomodulatory, anti-inflammatory, and tissue-reparative properties of MSC. To date, MSC-based products have been approved for the treatment of acute GVHD (aGVHD) in several countries, including China. Although MSC therapy is generally well tolerated, its broader clinical application remains challenged by substantial interindividual variability in therapeutic response, potential safety concerns, and the lack of harmonized standards for manufacturing and quality control. This review systematically summarizes recent clinical research on MSC-based interventions for GVHD and critically discusses their therapeutic prospects and current limitations, with the aim of informing standardized and precision-oriented clinical application of MSC therapy.

间充质干细胞治疗移植物抗宿主病的研究进展
移植物抗宿主病(GVHD)仍然是同种异体造血干细胞移植后的严重并发症,有效的治疗选择仍然有限,特别是对于类固醇难治性GVHD患者或多线治疗失败的患者。由于间充质干细胞(MSC)具有低免疫原性、免疫调节、抗炎和组织修复的特性,因此MSC治疗在预防和治疗GVHD方面显示出了前景。迄今为止,基于msc的产品已在包括中国在内的多个国家被批准用于治疗急性GVHD (aGVHD)。尽管骨髓间充质干细胞治疗通常耐受性良好,但其更广泛的临床应用仍然受到治疗反应的个体差异、潜在的安全问题以及缺乏统一的生产和质量控制标准的挑战。本文系统总结了近年来基于MSC干预GVHD的临床研究,并批判性地讨论了其治疗前景和目前的局限性,旨在为MSC治疗的标准化和精准化临床应用提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.80
自引率
0.00%
发文量
100
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