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血液系统恶性肿瘤的干细胞移植:个性化医疗及与间充质干细胞联合治疗的前景

Stem Cell Transplantation for Hematological Malignancies: Prospects for Personalized Medicine and Co-therapy with Mesenchymal Stem Cells.

作者信息

Patel Shyam A, Rameshwar Pranela

机构信息

Department of Medicine, Division of Hematology/Oncology, New Jersey Medical School, University of Medicine and Dentistry of New Jersey, Newark, NJ, USA.

出版信息

Curr Pharmacogenomics Person Med. 2011 Sep 1;9(3):229-239. doi: 10.2174/187569211796957548.

Abstract

Bone marrow transplantation is a form of cell therapy that has been in practice for decades for the treatment of hematological disorders and solid tumors. Immunosuppressive therapy has been a mainstay for treatment, but the severity of the adverse effects has made it an undesirable choice. Mesenchymal stem cells (MSCs), which reside in the vascular regions of the bone marrow, have been shown to serve as cellular support for the hematopoietic stem cell (HSC) niche. Furthermore, the immune suppressive properties of MSCs have been explored in the treatment of inflammatory and autoimmune disorders. Thus, co-therapy with MSCs has been shown to facilitate engraftment of hematopoietic cells by suppressive graft versus host disease (GvHD). Although the mechanism by which MSCs suppress GvHD is unclear, the experimental evidence suggests that this partly occurs by modulation of immune response such as the induction of regulatory T cells. This paper discusses the role of MSCs as co-therapy for the future of stem cell transplantation, with the overarching theme of personalized medicine for cell-based health interventions.

摘要

骨髓移植是一种细胞治疗形式,几十年来一直在实践中用于治疗血液系统疾病和实体瘤。免疫抑制疗法一直是主要的治疗方法,但不良反应的严重性使其成为一个不理想的选择。间充质干细胞(MSC)存在于骨髓的血管区域,已被证明可为造血干细胞(HSC)微环境提供细胞支持。此外,MSC的免疫抑制特性已在炎症和自身免疫性疾病的治疗中得到探索。因此,与MSC联合治疗已被证明可通过抑制移植物抗宿主病(GvHD)促进造血细胞的植入。虽然MSC抑制GvHD的机制尚不清楚,但实验证据表明,这部分是通过调节免疫反应,如诱导调节性T细胞来实现的。本文讨论了MSC作为联合治疗在干细胞移植未来中的作用,其总体主题是基于细胞的健康干预的个性化医学。

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