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TGF-β_1受体阻滞剂对树突状细胞融合疫苗制备的影响研究 被引量:1

Effect of TGF-β_1 Receptor Blocker on Fusion Vaccine of Dendritic Cells
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摘要 目的探讨TGF-β1受体阻滞剂SB-431542对树突状细胞(DC)融合疫苗制备的影响。方法①SB-431542(TGF-β1受体阻滞剂)与粒细胞集落刺激因子(GM-CSF)、白细胞介素-4(IL-4)、脂多糖(LPS)联合应用,刺激C57BL/6小鼠骨髓来源DC成熟,应用聚乙二醇(PEG)融合技术融合DC和小鼠胰腺癌细胞(Panc02),制备融合疫苗。②观察细胞形态、细胞表面表达、MTT法检测肿瘤细胞体外杀伤细胞毒活性。结果①在SB-431542参与下,成熟DC的细胞数目及形态无显著改变;②DC表面CD80、CD86、CD40的表达较未加SB-431542显著增高;MTT比色法,添加SB-431542的DC疫苗组对肿瘤细胞的杀伤抑制率显著提高。结论 SB-431542组融合细胞的分子表达较非SB-431542组显著提高;体外MTT显示SB-431542组有更好的抗肿瘤效应,说明SB-431542对增强融合疫苗抗肿瘤效应有明显的增强作用。 Objective To investigate the effect of SB-431542 on the preparation of the dendritic cell fusion vaccine. Methods ①In the presence of SB-431542(an inhibitor TGF- β1 receptor), GM-CSF, IL-4 and LPS, the maturation of dendritic cells from C57BL/6 mouse bone marrow was stimulated,and the preparation of the fusion vaccine was made by use of polyethylene glycol(PEG) fusion technique for fusion of DC and mouse pancreatic cells(Panc02). ②The observation of cell morphology and expression of cell surface phenotypes and the MTY assay detection of specific cytotoxic Tlymphocyte(CTL)were carried out. Results ①SB-431542 could stimulate the full maturation of dendritic cells. Dendritic cells and panc02 cells could be fused by PEG. ②The fusion cells exhibited typical biological characteristics. The expression of cell surface phenotypes was enhanced efficiently. Conclusion SB-431542 can enhance the maturation of dendritic cell. The fusion vaccine could induce a specific and effective immune response against tumor cell.
作者 任建林 徐钧
出处 《中国现代医生》 2010年第14期17-18,21,F0003,共4页 China Modern Doctor
关键词 树突状细胞 细胞融合 SB-431542 肿瘤疫苗 Dendritic cells Cell fusion SB-431542 Cancer vaccine
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  • 1Juan Zhang~1 Jin-Kun Zhang~2 Shao-Hong Zhuo~3 Hai-Bin Chen~2 1 Clinical Laboratory,The First Affiliated Hospital of Shantou University Medical College,Shantou 515041,Guangdong Province,China2 Cancer Pathology Laboratory,Shantou University Medical College,Shantou 515031,Guangdong Province,China3 Department of Gastroenterology,Third Municipal Hospital of Shantou,Shantou 515073,Guangdong Province,China.Effect of a cancer vaccine prepared by fusions of hepatocarcinoma cells with dendritic cells[J].World Journal of Gastroenterology,2001,7(5):690-694. 被引量:26
  • 2于哲,范清宇.树突状细胞肿瘤疫苗的研究进展[J].医学研究生学报,2005,18(1):63-66. 被引量:8
  • 3Massague J. The transforming growth factor-bets family[J]. Annu Rev Cell Biol,1990,6:597-641.
  • 4Munger JS, Harpel JG, Gleizes PE, et al. Latent transforming growth factor-B;Structural factures and mechanisms of activation [ J ]. Kidney Int, 1997,51 (5) : 1376-1382.
  • 5Taipale J, Keskioja J. Growth factors in the extracellular matrix [J]. FASEB J, 1997,11 : 51-59.
  • 6Hinch AP, Archer S J, Qian SW, et al. Transforming growth factor-beta 1; three-dimensional structure in solution and comparision with the X-ray structure of transforming growth factor-beta 2 [ J ]. Biochemstry, 1996,35:8517-8534.
  • 7Roberls AB. TGF-beta singaling from receptors to the nueleus [ J ]. Mierobers Infect, 1999,15 : 1265-1273.
  • 8Warner DR, Roberts EA, Greene RM, et al. Identifieation of novel Smad binding proteins [ J ]. Biochem Biophys Res Commun,2003,312(4) :1185-1190.
  • 9Kuang C, Chen Y. Tumor derived C-terminal mutations of Smad4 with decreased DXA binding activity and enhaneed intramolecular interacion [ J ]. Oneogene, 2004, 23 ( 5 ) : 1021-1029.
  • 10De Caestecker MP, Pick E, Roberts AB. Role of transforming growth factor-beta singaling in cancer [ J ]. J Natl Cancer Inst,2000,92 (17) : 1388-1402.

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  • 1温宗梅,戚中田.肿瘤DNA疫苗:诱导抗肿瘤抗原的CTL应答[J].国际生物制品学杂志,2006,29(5):216-218. 被引量:2
  • 2Eager R, Nemunaitis J. GM-CSF gene-transduced tumor vaccines[ J]. Molecular Therapy, 2005,12( 1 ) :18-27.
  • 3Ozgen A. A single institution retrospective analysis of ma- lignant melanoma[J]. J Cancer lies Ther, 2014, I0( 1 ) : 38-42.
  • 4Korgavkar K, Lee K C, Weinstock M A. Higher melano- ma incidence in coastal versus inland counties in Califor- nia[ J]. Melanoma Res, 2014,24(3) :280-285.
  • 5Bai Y, Burchfield R, Lu S, et al. Bacteria-Based Vec- tors for Oral Gene Therapy[ M]. New York: Mucosal De- livery of Biopharmaceuticals. Springer. 2014: 313-324.
  • 6Shata M T, Stevceva L, Agwale S, et al. Recent ad- vances with recombinant bacterial vaccine vectors [ J ]. Molecular medicine today, 2000,6(2) :66-71.
  • 7Low K B, Ittensohn M, Le T, et al. Lipid A mutant Sal- monella with suppressed virulence and TNFoL induction retain tumor-targeting in vivo [ J ].Nature biotechnology, 1999,17(1) :37-41.
  • 8Kong W, Clark-Curtiss J, Curtiss R, et al. Utilizing Sal- monella for antigen delivery: the aims and benefits of bacterial delivered vaccination[ J]. Expert Rev Vaccines, 2013,12(4) :345-347.
  • 9Grille S, Moreno M, Brugnini A, et al. A therapeutic vaccine using Salmonella-modified tumor cells combined with interleukin-2 induces enhanced antitumor immunity in B-cell lymphoma [ J ]. Leukemia research, 2013,37 (3) :341-348.
  • 10Wang S, Li Y, Shi H, et al. Comparison of a regulateddelayed antigen synthesis system with in vivo-inducible promoters for antigen delivery by live attenuated Salmo- nella vaccines [J]. Infection and immunity, 2011,79 (2) :937-949.

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