Lee Hong Kyung, Lim Sang Hee, Chung In Sung, Park Yunsoo, Park Mi Jeong, Kim Ju Young, Kim Yong Guk, Hong Jin Tae, Kim Youngsoo, Han Sang-Bae
College of Pharmacy, Chungbuk National University, Cheongju 361-763, Korea.
Immune Netw. 2014 Apr;14(2):81-8. doi: 10.4110/in.2014.14.2.81. Epub 2014 Apr 21.
Mesenchymal stem cells (MSCs) are present in diverse tissues and organs, including bone marrow, umbilical cord, adipose tissue, and placenta. MSCs can expand easily in vitro and have regenerative stem cell properties and potent immunoregulatory activity. They inhibit the functions of dendritic cells, B cells, and T cells, but enhance those of regulatory T cells by producing immunoregulatory molecules such as transforming growth factor-β, hepatic growth factors, prostaglandin E2, interleukin-10, indolamine 2,3-dioxygenase, nitric oxide, heme oxygenase-1, and human leukocyte antigen-G. These properties make MSCs promising therapeutic candidates for the treatment of autoimmune diseases. Here, we review the preclinical studies of MSCs in animal models for systemic lupus erythematosus, rheumatoid arthritis, Crohn's disease, and experimental autoimmune encephalomyelitis, and summarize the underlying immunoregulatory mechanisms.
间充质干细胞(MSCs)存在于多种组织和器官中,包括骨髓、脐带、脂肪组织和胎盘。MSCs在体外易于扩增,具有再生干细胞特性和强大的免疫调节活性。它们抑制树突状细胞、B细胞和T细胞的功能,但通过产生免疫调节分子如转化生长因子-β、肝生长因子、前列腺素E2、白细胞介素-10、吲哚胺2,3-双加氧酶、一氧化氮、血红素加氧酶-1和人类白细胞抗原-G来增强调节性T细胞的功能。这些特性使MSCs成为治疗自身免疫性疾病的有前景的治疗候选物。在此,我们综述了MSCs在系统性红斑狼疮、类风湿性关节炎、克罗恩病和实验性自身免疫性脑脊髓炎动物模型中的临床前研究,并总结了潜在的免疫调节机制。