期刊文献+

调节性树突状细胞诱导大鼠供者特异性移植物免疫低反应

Regulatory dendritic cells treatment induce donor-specific allograft hyporesponsiveness
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摘要 目的探讨调节性树突状细胞(rDC)对大鼠同种异体排斥反应的调控及其效应。方法大鼠腹腔心脏移植前7d,受者静脉输注供者来源未成熟DC(imDC)、成熟DC(matDC)、rDC和磷酸盐缓冲液(PBS)。观察移植物体存活时间,比较排异反应病理分级,逆转录聚合酶链反应(RT—PCR)检测受者淋巴结细胞叉状头/翅膀状螺旋转录因子(Foxp3)mRNA表达。结果rDC组(18.6d)移植物平均生存时间较imDC(12.1d)、matDC(6.8d)和PBS(7.1d)组显著延长(P〈0.05)。检测受者淋巴结组织中Foxp3mRNA的表达结果显示:PBS组几乎不表达,matDC组表达较低,imDC组和rDC组表达明显上调,与前两组比较差异有统计学意义(P〈0.01),但两者间差异无统计学意义(P〉0.05)。结论rDC能延长同种异体大鼠心脏移植物的存活时间,诱导受者对供者移植物的特异性免疫低反应。 Objective To investigate the effect and mechanism of regulatory dendritic cell (rDC) in allograft rejection. Methods Graft recipients were infused (i. v. ) with 1×10^6 rDC, imature dendritic cell (imDC) , MatDC or PBS respectively 7 days preceding heterotopie fully MHC-mismatched heart trans- plantation. Graft survival was monitored by transabdominal palpation of the donor heart. The forkhead box P3(Foxp3) mRNA expression was determined in lymph node eells at day 7 after the i. v. infusion by re- verse transcriptase-polymerase chain reaction (RT-PCR). The sample of allogr'aft had been studied by he- matoxylin and eosin (HE) stain and scored according to the International society of Heart. Results rDC prolonged the mean survival time (MST) of allograft, which was 18.6 days, as compared to PBS group (7. l days; P〈0.01), imDC group (12.1 days; P〈0.05) and matDC group (6.8 days; P〈0.01), respectively. Infusion of rDC and imDC resulted in increased foxp3 mRNA expression as compared to infusion of matDC and PBS, respectively. Conclusion Pretreatment with donor type rDC resulted in pro- longed survival of a completely MHC-mismatched heart allograft, rDC is more efficacious than the classical imDC in the regulation of the alloimmune response.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2013年第6期1200-1202,共3页 Chinese Journal of Experimental Surgery
关键词 调节性树突状细胞 器官移植 排异反应 Regulatory dendritic cell Organ transplantation Allografl rejection
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参考文献10

  • 1Lutz MB,Schuler G. hnmature,semi-mature and fully mature dendrit- ic cells:which signals induce tolerance or immunity? Trends Immu- no1,2002 ,23 :445-449.
  • 2Matyszak MK, Citterio S, Rescigno M, Ricciardi-Castagnoli P. Difir- ential effects of corticosteroids during different stages of dendritic cell maturation. Eur J Immunol, 2000,30:1233-1242.
  • 3Roelen DL, Schuurhuis DH, van den Boogaardt DE, et al. Prolongation of skin graft survival by modulation of the alloimmune response with alternatively activated dendritic cells. Transplantation, 2003,76 : 1608- 1615.
  • 4高晓燕,黄必军,丘惠娟.大鼠调节性树突状细胞的培养与生物学特性鉴定[J].中华实验外科杂志,2012,29(11):2252-2254. 被引量:1
  • 5尧凯,高晓燕,董培,王祥慧,徐达,周芳坚,韩辉.改良大鼠腹腔心脏移植模型的建立[J].中华实验外科杂志,2012,29(11):2323-2324. 被引量:2
  • 6McCurry KR, Colvin BL, Zahorchak AF, et al. Regulatory dendritic cell therapy in organ transplantation. Transpl Int.2006.19:525-529.
  • 7Roelen DL, Schuurhuis DH, van den Boogaardt DE, et al. Prolongation of skin graft survival by modulation of the alloimmune response with ahernatively activated dendritic cells. Transplantation, 2003,76 : 1608- 1615.
  • 8Oehando JC, Yopp AC, Yang Y, et al. Lymph node occupancy is re- quired for the peripheral development of alloantigen-specific Foxp3 + regulatory T cells. J Immuno1,2005,174:6993-7005.
  • 9Cobbold SP, Nolan KF, Graca L,et al. Regulatory T ceils and dendrit- ic cells in transplantation tolerance: molecular markers and mecha- nisms. Immunot Rev ,2003,196 : 109-124.
  • 10Hawiger D, Inaba K, Dorsett Y, et al. Dendritic cells induce peripheral T cell unresponsiveness under steady state conditions in vivo. J Exp Med ,2001,194:769-775.

二级参考文献14

  • 1马毅,陈细桃,朱晓峰,何晓顺,陈规划.大鼠异位心脏移植模型的术式探讨[J].中华实验外科杂志,2005,22(10):1238-1240. 被引量:15
  • 2李跃华,陈凡,宋惠民.两种大鼠异位心脏移植模型的比较[J].中华实验外科杂志,1997,14(2):114-115. 被引量:5
  • 3Morelli AE,Thomson AW. Dendritic cells:regulators of alloimmunity and opportunities for tolerance induction. Immunol Rev, 2003,196 : 125-146.
  • 4Lutz MB, Schuler G. Immature, semi-mature and fully mature dendrit- ic cells:which signals induce tolerance or immunity?. Trends Immu- no1,2002 ,23 :445-449.
  • 5Hackstein H,Thomson AW. Dendritic cells : emerging pharmacological targets of immunosuppressive drugs. Nat Rev Immunol, 2004,4 : 24- 29.
  • 6Lu L, McCaslin D, Starzl TE, et al. Bone marrow-derived dendritic cell progenitors induce alloantigen-specific hyporesponsiveness in murine T lymphocytes. Transplantation, 1995,60 : 1539-1544.
  • 7Xing N, ML LM, Bachman LA, et al. Distinctive dendritic cell modu- lation by vitamin D (3) and glucocorticoid pathways. Biochem Bio- phys Res Commun 2002,297:645-652.
  • 8Lutz MB. Immature, semi-mature and fully mature dendritic cells: which signals induce tolerance or immunity. Trends Immunol,2002, 23:445-449.
  • 9Tone M, Powell MJ, Tone Y, et al. IL-10 gene expression is controlled by the transcription factors Spl and Sp3. J Imrnunol,2000,165:286- 291.
  • 10Brightbill HD, Plevy SE, Modlin RL, et al. A prominent role for Spl during lipopolysaccharide-mediated induction of the IL-10 promoter in macrophages. J Immuno1,2000,164 : 1940-1951.

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