期刊文献+

吉西他滨对胰腺癌外周血调节性T细胞影响的研究

Changes of regulatory T cells in peripheral blood after gemcitabine chemotherapy for pancreatic cancer patients
下载PDF
导出
摘要 目的探讨吉西他滨对胰腺癌外周血调节性T细胞的影响,为进一步提高过继免疫治疗的疗效提供依据和参考。方法本研究入选2012年1月至2014年10月收治的32例胰腺癌患者,分为吉西他滨组(吉西他滨+过继免疫治疗)和对照组(单纯过继免疫治疗),观察两组患者治疗前后外周血调节性T细胞水平、化疗不良反应,并对两组患者的生存时间进行分析比较。结果吉西他滨组患者治疗后外周血调节性T细胞水平较治疗前显著降低,与对照组相比亦显著降低,两组比较有统计学差异(P<0.05),吉西他滨组中位生存时间较对照组延长1.3个月(10.0个月与8.7个月比较)。结论吉西他滨化疗可以显著降低胰腺癌患者外周血调节性T细胞水平,有效调节患者的肿瘤免疫耐受,提高过继免疫治疗的疗效。 Objective To investigate the influence of gemcitabine chemotherapy on levels of regulatory Tcells (Tregs) in peripheral blood for patients with pancreatic cancer and provide evidence and reference for improving the efficacy of adoptive im-munotherapy .Methods 32 patients were enrolled in this study from January 2012 to October 2014 ,among whom 16 received gemcitabine chemotherapy combined with adoptive immunotherapy (gemcitabine group) ,the other 16 patients received adoptive immunotherapy only(control group) .The level of Tregs in peripheral blood ,side effect and overall survival were observed be-fore and after the therapy .Results The number of Tregs in peripheral blood was significantly decreased after gemcitabine chemotherapy ,and it was also lower than that of the control group .The overall survival time of the gemcitabine group was 1.3 mo longer than the control group(10 .0 mo vs 8 .7 mo) .Conclusion Therapeutic regimen of gemcitabine can remarkly de-plete Tregs in peripheral blood of patients with pancreatic cancer ,effectively regulate tumor immune tolerance ,and improve the efficacy of adoptive immunotherapy .
出处 《药学实践杂志》 CAS 2015年第3期258-260,268,共4页 Journal of Pharmaceutical Practice
基金 第二军医大学青年启动基金课题(2012QN18)
关键词 吉西他滨 胰腺癌 调节性T细胞 过继免疫治疗 gemcitabine pancreatic cancer regulatory T eells(Tregs) adoptive immunotherapy
  • 相关文献

参考文献12

  • 1Trouilloud I, Dubreuil O, Boussaha T,et al. Medical treatment pancreatic cancer: new hopes after 10 years of gemcitabine [J]. Clin Res Hepatol Gastroenterol,2011,35(5) :364-374.
  • 2ShevchenkoI,Karakhanova S, Soltek S,et al. Low-dose gemc- etabine depletes regulatory T cells and improves survival in the orthotopic Pane02 model of pancreatic cancer[J]. Int J Cancer,2013,133(1) :98-107.
  • 3Burris HA, Moore MJ, Andersen J ,et al. Improvement in sur- vival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer~ a randomized trial [J]. J Clin Onco1,1997,15(6) :2403-2413.
  • 4Hiraoka N, Onozato K, Kosuge T, et al. Prevalence of FOXP3+ regulatory T cells increases during the progression of pancreatic ductal adenocareinoma and its premalignant le- sions[J]. Clin Cancer Res, 2006,12 : 5423-5434.
  • 5Ikemoton T, Yamaguehi T, Morine Y, et al. Clinical roles of increased populations of Foxp3+ CD4+ T ceils in peripheral blood from advanced pancreatic cancer patients[J]. Pancreas, 2006,33 .. 386-390.
  • 6Shindo Y, Hazama S, Maeda Y,et al. Adoptive immunother- apy with MUCI-mRNA transfeeted dendritic cells and cyto- toxic lymphoeytes plus gemcetabine for unresectable pancre- atic cancer[J]. J Translat Med, 2014,12 : 175.
  • 7Gabitass RF, Annels NE, Stocken DD, et al. Elevated myeloid- derived suppressor cells in pancreatic, esophageal and gastric cancer are an independent prognostic factor and are associated with significant elevation of the Th2 cytokine interleukin-13 [J]. Cancer Immunol Immunother, 2011,60 : 14,19-1430.
  • 8Ghansah T, Vohra N, Kinney K,et al. Dendritic cell immu- notherapy combined with gemcitabine chemotherapy enhances survival in a murine model of pancreatic carcinoma[J]. Cancer Immunol Immunother, 2013,62 : 1083-1091.
  • 9高强,邱双健,樊嘉.CD4^+CD25^+FOXP3^+调节性T细胞在肿瘤免疫逃逸中的作用研究进展[J].中国癌症杂志,2007,17(8):657-662. 被引量:13
  • 10卢晓婷,刘俊田.CD_4+CD_(25)+调节性T细胞在肿瘤免疫及化疗方面的研究进展[J].中国肿瘤临床,2008,35(11):656-658. 被引量:28

二级参考文献59

  • 1刘莉,姚军霞,丁乾,黄士昂.非霍奇金淋巴瘤患者外周血CD4^+CD25^(high)调节性T细胞研究[J].中国实验血液学杂志,2006,14(1):119-122. 被引量:30
  • 2Mukherji B,Wilhelm SA,Guha A,et al.Regulation of cellular immune response against autologous human melanoma.I.Evidence for cell-mediated suppression of in vitro cytotoxic immune response[J].J Immunol,1986,136(5):1888-1892.
  • 3Sakaguchi S,Sakaguchi N,Asano M,et al.Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains (CD25):breakdown of a single mechanism of self-tolerance causes various autoimmune diseases[J].J Immunol,1995,155(3):1151-1164.
  • 4Fontenot JD,Gavin MA,Rudensky AY.Foxp3 programs the development and function of CD4+CD25+ regulatory T cells[J].Nat Immunol,2003,4(4):330-336.
  • 5Williams LM,Rudensky AY.Maintenance of the Foxp3-dependent developmental program in mature regulatory T cells requires continued expression of Foxp3[J].Nat Immunol,2007,8(3):277-284.
  • 6Jonuleit H,Schmitt E.The regulatory T cell family:distinct subsets and their interrelations[J].J Immunol,2003,171(12):6323-6327.
  • 7Cozzo C,Lerman MA,Boesteanu A,et al.Selection of CD4+CD25+ regulatory T cells by self-peptides[J].Curr Top Microbiol Immunol,2005,293:3-23.
  • 8Chen W,Jin W,Hardegen N,et al.Conversion of peripheral CD4+CD25-naive T cells to CD4+CD25+ regulatory T cells by TGF-beta induction of transcription factor Foxp3[J].J Exp Med,2003,198(12):1875-1886.
  • 9Turk MJ,Guevara-Patino JA,Rizzuto GA,et al.Concomitant tumor immunity to a poorly immunogenic melanoma is prevented by regulatory T cells[J].J Exp Med,2004,200(6):771-782.
  • 10Peng L,Kjaergaard J,Plautz GE,et al.Tumor-induced L-selectinhigh suppressor T cells mediate potent effector T cell blockade and cause failure of otherwise curative adoptive immunotherapy[J].J Immunol,2002,169(9):4811-4821.

共引文献37

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部