基础医学与临床 ›› 2007, Vol. 27 ›› Issue (9): 1006-1010.

• 研究论文 • 上一篇    下一篇

慢性再生障碍性贫血患者间充质干细胞对T细胞的抑制作用

刘丽辉 孙昭 韩钦 叶丽萍 施兵 金建刚 赵春华   

  1. 解放军总医院第二附属医院血液科 医科院基础医学研究所 医科院基础医学研究所 解放军总医院第二附属医院血液科 解放军总医院第二附属医院血液科 解放军总医院第二附属医院血液科 医科院基础所
  • 收稿日期:2006-06-01 修回日期:2007-01-26 出版日期:2007-09-25 发布日期:2007-09-25
  • 通讯作者: 刘丽辉

Effects of T-cell suppression mediated by mesenchymal stem cells in patients with chronic aplastic anemia

Li-hui Liu Zhao Sun Qin Han Li-ping Ye Bing Shi Jian-gang Jin   

  • Received:2006-06-01 Revised:2007-01-26 Online:2007-09-25 Published:2007-09-25
  • Contact: Li-hui Liu

摘要: 目的 比较来源于正常志愿者和慢性再生障碍性贫血(CAA)患者骨髓间充质干细胞(MSC)免疫抑制作用的区别。方法 培养5例正常志愿者和10例CAA患者的骨髓MSC,比较两组MSC的形态、细胞表型、细胞因子的表达,通过PHA刺激的T细胞增殖试验,混合淋巴细胞培养和T细胞周期检测比较两组MSC对T细胞的抑制作用。结果 两组MSC形态、表型基本相同。CAA来源的MSC对PHA和同种异体抗原诱导的T细胞的抑制作用均低于正常志愿者来源的MSC,加入正常志愿者的MSC后有更多的T细胞阻滞在G0/G1期,但CAA来源的MSC作用较弱。两组MSC表达的肝细胞生长因子(HGF)、转化生长因子(TGF-β2)无明显区别,但CAA患者的MSC表达的TGF-β1、3较正常志愿者MSC表达的明显减少。结论 虽然CAA的MSC在形态、增殖和细胞表型上基本正常,但其对T细胞的抑制作用减弱,在经过免疫抑制剂治疗后仍然存在,其异常是否与CAA的发病机制有关需要进一步研究。

Abstract: Objectve To compare the effects of T-cell suppression mediated by mesenchymal stem cells (MSC) from normal individuals and chronic aplastic anemia (CAA) patients. Methods MSC were cultured from the bone marrow of 5 healthy volunteers and 10 CAA patients, Morphology, surface markers and the expression of serveral cytokines of MSC were compared, and the effects of T-cell supression were tested in the following assay: phytohemaglutinin (PHA)-primed cultures, mixed lymophocyte reaction (MLR) and cell cycle of T-cell after PHA-primed cultures. Results MSC from normal volunteers and CAA patients were similar in morphology, proliferation and surface markers. The suppression of T-cell proliferation induced by PHA and alloantigens mediated by CAA MSC was significantly lower than that of normal MSC. More T-cells were arrested in G0/G1 phase by normal MSC, while the effects were deficient by CAA MSC. The cytokines TGF-β2, HGF expression were similar in normal MSC and CAA MSC, but TGF-β1, 3, expressed by CAA MSC were reduced comparing with normal MSC. Conclusion Although the morphology, proliferation and cell surface markers of CAA MSC were normal, the T-cell suppression mediated by CAA MSC is deficient, persists indifinitely after immunosuppressive therapy, whether these abnormalitied are relevant to the pathogenesis of aplastic anemia remains to be determined.