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小鼠肝癌总RNA转染的树突状细胞体外诱导特异性细胞毒T淋巴细胞的研究 被引量:1

Anti-tumor responsiveness by dendritic cells transfected with tumor total RNA
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摘要 目的 :探讨小鼠骨髓树突状细胞 (dendriticcell,DC)体外经Hepa 1 6肝癌细胞株总RNA转染后 ,对特异性细胞毒T淋巴细胞 (CTL)的诱导作用。方法 :自小鼠骨髓分离DC前体细胞 ,经GM CSF +IL 4培养、扩增 ;制备Hepa 1 6小鼠肝癌细胞株总RNA ,体外转染DC ,检测DC诱导同基因型小鼠T细胞增殖及其特异性CTL的反应能力。结果 :经Hepa 1 6肝癌细胞总RNA转染的DC ,其组织相容性分子 (MHC I、II)及共刺激分子 (B7 1 、B7 2 )表达明显增高 ,刺激同基因型小鼠T细胞增殖能力增强 ,且能诱导Hepa 1 6特异性CTL。结论 :以肝癌总RNA转染DC ,构造肝癌疫苗为肝癌的临床治疗提供了新的策略。 Objective:The present study was designed to investigate whether transfecting DC with tumor derived total RNA is an effective way to induce CTL and antitumor immunity.Methods:DC were propagated from bone marrow(BM) of C57BL/6J(H 2k b?I A b)mice in vitro with GM CSF+IL 4.Tumor derived total RNA extracted from actively growing Hepa 1 6 cells was used to transfected DC.The phenotypes of DC were detected by FACS,the cytotoxicity of CTL was assayed by MTT method.Results:The tumor derived total RNA transfected DC exhibited much more and longer plasm membrane processes and increased expression of MHC Ⅰ?MHC Ⅱ?CD80(B7 1)?CD86(B7 2).Conclusion:This experiment has shown that DC transfected with tumor derived total RNA of C57BL/6J cells could stimulate effectively the responsiveness of syngenic splenic T cells to induce specific CTL against C57BL/6J cells.
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2002年第2期102-105,共4页 Chinese Journal of Immunology
基金 国家自然科学基金 (3 9770 3 87) 1999年高校博士点基金(983 9)资助
关键词 树突状细胞 肝癌 核糖核酸 细胞毒T淋巴细胞 动物实验 RNA转染 Dendritic cells Hepatocarcinoma RNA Cytotoxic of T lymphocytes
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  • 1吴厚生.用^3H-TdR释放法测量细胞介导的细胞毒功能[J].上海免疫学杂志,1987,(4):230-233.
  • 2[1] Thomson A W, Lu L.Are dendritic cells the key to liver transplant t olerance [J]? Immunology today, 1999,20(1):27-32.
  • 3[2] Khanan A, Morelli A E, Zhong CP, et al. Effects of liver-derved de ndritic cell progenitors on Thl-and Th2 like cytokine responses in vitor and in vivo. The Journal of Immunology,2000,164(3):1346-1354.
  • 4[3] Lu L, Woo J, Rao A S, et al. Propagation of dendritic cell progenit ors from n ormal mouse liver using granulocyte/macrophage colony-stimulating factor and th e ir maturational development in the presence of type-l collagen[J]. J Exp Med, 1994,179(6):1823-1834.
  • 5[4] Inaba K, Inaba M, Romani N, et al. Generation of large numb er of dendritic c ells from mouse bone marrow cultures supplemented with Granulocyte/Macrophage co lony-stimulating factor[J]. J Exp Med, 1992,176(6):1693-1702.
  • 6[5] Smedt T D, Mechelen M V, Becker G D, et al. Effect of interleukin- 1 0 on dendritic cell maturation and function[J]. Eur, J Immunol,1997,27(5):1229 -1235.
  • 7[6] Rissoan MC, Soumelis V,Kadowaki N,et al. Reciprocal control of T he lper cell and dendritic cell differentiation[J]. Science, 1999,283(5405):1183-1186 .
  • 8[2]Bandchereav J,Steinman RM.Dendritic cells and the control of immun ity[J]. Nature,1998,392(19):245251.
  • 9[3]Flamand.V,Sornasse T,Thielemans K,et al.Murine dendritic cells pul sed in vitro with tumor antigen induce tumor resistance in vivo[J].Europ J Immunol,19 94 24(3):605-610.
  • 10[4]Nair SK,Snyder D,Rouse BT,et al.Regression of tumors in mice vacci nated w ith professional antigen-presenting cells pulsed with tumor extracts[J].Int J Cancer,1997,70(6):706-715.

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