Hematti Peiman
Department of Medicine, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, WI 53792, USA.
Transplant Rev (Orlando). 2008 Oct;22(4):262-73. doi: 10.1016/j.trre.2008.05.002. Epub 2008 Jul 24.
Mesenchymal stromal cells (MSCs) originally isolated from bone marrow have been derived from almost every tissue in the body. These multipotent cells can be differentiated in vitro and in vivo into various cell types of mesenchymal origin, such as bone, fat, and cartilage. Furthermore, under some experimental conditions, these cells can differentiate into a wider variety of cell types. Upon systemic administration, ex vivo expanded MSCs preferentially home to damaged tissues and participate in regeneration processes through their diverse biological properties. In vitro and in vivo data suggest that MSCs have low inherent immunogenicity and modulate/suppress immunologic responses through interactions with different immune cells. Ease of isolation and ex vivo expansion of MSCs, combined with their intriguing differentiation and immunomodulatory potential, and their impressive record of safety in clinical trials make these cells prime candidates for cellular therapy. Mesenchymal stromal cells derived from bone marrow are currently being evaluated for a wide range of clinical applications including for treatment of immune dysregulation disorders such as acute graft-versus-host disease after allogeneic hematopoietic stem cell transplantation. In the future, MSCs might potentially provide novel therapeutic options for treatment/prevention of rejection and/or repair of organ allografts through their multifaceted properties.
最初从骨髓中分离出的间充质基质细胞(MSC)几乎可源自身体的每个组织。这些多能细胞在体外和体内均可分化为多种间充质来源的细胞类型,如骨、脂肪和软骨。此外,在某些实验条件下,这些细胞可分化为更多种类的细胞类型。经体外扩增后全身给药时,MSC会优先归巢至受损组织,并通过其多样的生物学特性参与再生过程。体外和体内数据表明,MSC具有较低的固有免疫原性,并通过与不同免疫细胞的相互作用调节/抑制免疫反应。MSC易于分离和体外扩增,再加上其引人关注的分化和免疫调节潜能,以及在临床试验中令人印象深刻的安全记录,使其成为细胞治疗的理想候选者。源自骨髓的间充质基质细胞目前正在广泛的临床应用中接受评估,包括用于治疗免疫失调疾病,如异基因造血干细胞移植后的急性移植物抗宿主病。未来,MSC可能通过其多方面特性为器官同种异体移植的排斥反应治疗/预防和/或修复提供新的治疗选择。