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[间充质干细胞与免疫调节:迈向治疗自身免疫性疾病的新型免疫抑制策略?]

[Mesenchymal stem cells and immunomodulation: toward new immunosuppressive strategies for the treatment of autoimmune diseases?].

作者信息

Larghero J, Vija L, Lecourt S, Michel L, Verrecchia F, Farge D

机构信息

Unité de thérapie cellulaire, Hôpital Saint-Louis, AP-HP, Paris, France.

出版信息

Rev Med Interne. 2009 Mar;30(3):287-99. doi: 10.1016/j.revmed.2008.08.019. Epub 2008 Oct 17.

Abstract

Mesenchymal stem cells (MSC) represent a population of the bone marrow microenvironment, which participates in the regulation of haematopoietic stem cells (HSC) self-renewal and differentiation. MSC are multipotent non-haematopoietic progenitors, which have been explored as a promising treatment in tissue regeneration. Both in vitro and in vivo, the MSC inhibit the T, B, NK and dendritic cell functions. Although MSC immunomodulating properties are not yet completely understood, their low immunogenic potential can be used as a therapeutic tool not only for regenerative medicine, but also for the treatment of graft-versus-host disease (GVHD) after bone marrow transplantation as well as for specific cases of severe refractory autoimmune diseases. Experimental and clinical data gave encouraging results, showing that MSC injection allowed controlling refractory GVHD, restoring bone development in children with osteogenesis imperfecta or improving heart function after myocardial infarction. Phase I-II studies are in progress in various countries to investigate the potential benefit from MSC due to their immunosuppressive properties, as an adjunctive therapy for severe refractory autoimmune disease.

摘要

间充质干细胞(MSC)是骨髓微环境的一部分,参与造血干细胞(HSC)自我更新和分化的调节。MSC是多能非造血祖细胞,已被探索作为组织再生中有前景的治疗方法。在体外和体内,MSC均抑制T细胞、B细胞、自然杀伤细胞(NK)和树突状细胞的功能。尽管MSC的免疫调节特性尚未完全明确,但其低免疫原性潜力不仅可作为再生医学的治疗工具,还可用于治疗骨髓移植后的移植物抗宿主病(GVHD)以及特定严重难治性自身免疫性疾病病例。实验和临床数据给出了令人鼓舞的结果,表明注射MSC可控制难治性GVHD、恢复成骨不全儿童的骨骼发育或改善心肌梗死后的心脏功能。各国正在进行I-II期研究,以调查由于MSC的免疫抑制特性作为严重难治性自身免疫性疾病辅助治疗可能带来的益处。

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