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用于肝硬化的间充质干细胞疗法:间充质干细胞作为改善肝纤维化和再生的“传导细胞”

Mesenchymal stem cell therapies for liver cirrhosis: MSCs as "conducting cells" for improvement of liver fibrosis and regeneration.

作者信息

Tsuchiya Atsunori, Takeuchi Suguru, Watanabe Takayuki, Yoshida Tomoaki, Nojiri Shunsuke, Ogawa Masahiro, Terai Shuji

机构信息

Division of Gastroenterology and Hepatology, Graduate School of Medical and Dental Science, Niigata University, 1-757 Asahimachi-dori, Chuo-ku, Niigata, 951-8510 Japan.

出版信息

Inflamm Regen. 2019 Sep 9;39:18. doi: 10.1186/s41232-019-0107-z. eCollection 2019.

Abstract

Mesenchymal stem cells (MSCs) can be cultured relatively easily and can be obtained not only from the bone marrow, but also from medical waste such as adipose tissue and umbilical cord tissue. Because of its low antigenicity, allogeneic MSC injection is safe. MSCs have been evaluated in more than 900 clinical trials in a variety of fields, with more than 50 clinical trials related to liver diseases. Experiments have suggested that MSCs function as "conducting cells" to affect various "effective cells" such as T cells, B cells, and macrophages. Recent clinical trials have focused on allogeneic MSCs. Thus, studies are needed to determine the most effective cell source, culture conditions, cell numbers, administration frequency, administration route, cost, safety, and liver disease treatments. Recently, the functions of exosomes have gained attention, and cell-free therapy may become possible as an alternative therapy for liver disease. In this review, we introduce general information, mechanism, representative clinical study data, recently started or planned clinical trials, and possibility of cell-free therapy of MSCs.

摘要

间充质干细胞(MSCs)相对易于培养,不仅可以从骨髓中获取,还可以从脂肪组织和脐带组织等医疗废弃物中获得。由于其低抗原性,同种异体间充质干细胞注射是安全的。间充质干细胞已在900多项涉及多个领域的临床试验中得到评估,其中有50多项与肝脏疾病相关的临床试验。实验表明,间充质干细胞作为“传导细胞”影响各种“效应细胞”,如T细胞、B细胞和巨噬细胞。最近的临床试验集中在同种异体间充质干细胞上。因此,需要开展研究以确定最有效的细胞来源、培养条件、细胞数量、给药频率、给药途径、成本、安全性以及肝脏疾病的治疗方法。最近,外泌体的功能受到关注,无细胞疗法可能成为肝脏疾病的一种替代治疗方法。在这篇综述中,我们介绍间充质干细胞的一般信息、作用机制、代表性临床研究数据、最近启动或计划开展的临床试验以及无细胞疗法的可能性。

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