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FTY720对小肠移植物中淋巴细胞及单核细胞浸润的影响

The effects of FTY720 on lymphocytes and monocytes in mouse intestinal transplantation

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【作者】 严盛于吉人刘小孙吴丽花郑树森

【Author】 YAN Sheng,YU Ji-ren,LIU Xiao-sun,WU Li-hua,ZHENG Shu-sen (Department of Surgery,The First Affiliated Hospital,Zhejiang University School of Medicine,Hangzhou 310003,China)

【机构】 浙江大学医学院附属第一医院普外科浙江大学医学院附属第一医院普外科 浙江杭州310003浙江杭州310003

【摘要】 目的:研究FTY720对同种异体小鼠小肠移植排斥反应的作用及可能机制。方法:以C3H小鼠(H-2k)为供者,C57BL/6小鼠(H-2b)为受者,行异位小肠移植。分别建立FTY720治疗组、空白对照组及同系移植组,在移植后6 d与12 d进行组织学观测评定排斥分数,流式细胞术分析移植物肠系膜淋巴结(MLN)、派氏结(PP)、粘膜上皮细胞间淋巴组织(IEL)与固有层淋巴组织(LPL)中淋巴细胞中受者淋巴细胞及单核细胞浸润情况。结果:FTY720在移植后6 d可有效抑制排斥反应,但在移植后14 d,排斥反应仍可发生。在空白对照组,移植后6 d移植物内受者淋巴细胞基本取代供者细胞;而在FTY720治疗组,受者淋巴细胞进入移植物的速度及数量明显减缓,包括CD4+与CD8+T细胞,以及CD19+B细胞。受者来源的γδT淋巴细胞也显著减少。FTY720对G r1+CD11b+单核细胞系也有一定的抑制作用。结论:FTY720可通过减少受者淋巴细胞及单核细胞进入移植小肠,起到缓解排斥反应的作用。

【Abstract】 AIM: To test the effects of FTY720 on mouse intestinal allografts.METHODS: C3H mice(H-2k)were used as donor and C57BL/6 mice(H-2b) as recipients.FTY720 group,allogeneic control group and isogeneic control group were set up.6 and 14 days after transplantation,murine intestinal grafts were harvested for histologic assessment.Lymphocytes were collected from mesenteric lymph nodes(MLN),Peyer’s patch(PP),lamina propria lymphocytes(LPL) and intraepithelial lymphocytes(IEL) in the graft,then were analyzed by cytometry.RESULTS: Rejection was inhibited in FTY720 group at the 6th post-transplant day,although not at the 14th day.Recipient CD4+ and CD8+ T cells,CD19+ B cells,as well as γδ TCR lymphocytes,were greatly reduced by FTY720 therapy.The similar action of FTY720 was also revealed in Gr1+CD11b+ monocytes.CONCLUSION: FTY720 is efficient on alleviating allo-immune response by reducing the infiltration of both lymphocytes and monocytes into the graft in a mouse intestinal transplantation model.

【关键词】 肠移植淋巴细胞单核细胞FTY720
【Key words】 Intestinal transplantationLymphocytesMonocytesFTY720
【基金】 国家自然科学基金资助(No.30471633);浙江省教育厅回国留学人员启动基金资助(No.J20040193);浙江省医药卫生科学研究基金资助(No.2003A023)
  • 【文献出处】 中国病理生理杂志 ,Chinese Journal of Pathophysiology , 编辑部邮箱 ,2006年08期
  • 【分类号】R656.7
  • 【下载频次】102
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