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协同刺激分子B7-H4与CD11c共表达对细胞因子诱导的杀伤细胞治疗胃癌患者预后的影响 被引量:1

Effects of coexpression of B7-H4 and CD11c on prognosis of patients with gastric cancer treated by cytokine-induced killer cells
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摘要 目的 观察协同刺激分子B7-H4及黏附分子CD11c在胃癌组织中的不同表达水平,并观察其对细胞因子诱导的杀伤细胞(CIK)治疗对胃癌患者预后的影响.方法 应用免疫组织化学法检测88例胃癌患者手术标本中B7-H4及CD11c的表达水平.采用x2检验比较CIK联合化疗组与单纯化疗组患者临床资料的均衡性.采用Kaplan-Meier法和Log-rank检验比较B7-H4、CD11c不同表达水平及CIK联合化疗、单纯化疗患者无瘤生存期及生存期的差异.采用多因素Cox模型分析B7-H4、CD11c不同表达水平联合CIK治疗与复发和死亡的关联强度.结果 CIK联合化疗组和单纯化疗组除在肿瘤转移差异有统计学意义外,其余临床资料及B7-H4、CD11c表达水平在两组间分布差异无统计学意义(P>0.05).CIK联合化疗+CD11c高表达+B7-H4低表达患者无瘤生存期及生存期明显高于单纯化疗+ CD11c低表达+B7-H4高表达患者(59个月比15个月、67个月比22个月,P<0.01).调整了性别、年龄、TNM分期、肿瘤分化程度、肿瘤大小等混杂因素后,与CIK联合化疗+ CD11c高表达+B7-H4低表达组比较,单纯化疗+CD1 1c低表达+B7-H4高表达组患者的复发率和死亡率明显升高,其风险比(HR)[95%可信区间(CI)]分别为5.06(1.64 -15.56)、6.51(2.09 -20.29).结论 CD11c高表达、B7-H4低表达胃癌患者接受CIK联合化疗的治疗方案将可能延长无瘤生存时间及生存时间. Objective To investigate the effects of the expression level of costimulatory molecules B7-H4 and adhesion molecules CD11c combined with cytokine-induced killer cells (CIK) therapy on the prognosis of patients with gastric cancer.Methods Tissue specimens from 88 cases of gastric cancer were evaluated for the expression levels of B7-H4 and CD11c by immunohistochemistry.The balance of clinical data between CIK therapy combined with chemotherapy group and chemotherapy group was evaluated by using chi-square test.Median disease-free survival time and median survival time in patients with different expression levels of B7-H4,CD11 c and methods of treatment were compared by using Kaplan-Meier and Log-rank test.The Cox model was used to evaluate the hazard risk (HR) of the link strength between the different expression levels of B7-H4 and CD11c combined with CIK therapy and recurrence,mortality.Results There was no significant difference in clinical data and expression levels of B7-H4 and CD11c between CIK combined with chemotherapy group and single chemotherapy group except metastasis.The median disease-free time and median survival time were significant difference between CIK combined with chemotherapy group + CD1 1c high + B7-H4 low and chemotherapy group + CD11 c low + B7-H4 high (P 〈0.01).Adjusted for sex,age,TNM stage,tumor differentiation,and tumor size,the recurrence and mortality were higher in single chemotherapy group + CD1 1c low + B7-H4 high as compared with CIK combined with chemotherapy group + CD11 c high + B7-H4 low (59 months vs.15 months,67 months vs.22months) with the HR value [95% confidence interval (CI)] being 5.06 (1.64-15.56) and 6.51(2.09-20.29) respectively.Conclusion Patients with high expression of CD11 c and low expression of B7-H4 in combination with the CIK chemotherapy may prolong disease-free survival time and survival time.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2015年第3期460-462,共3页 Chinese Journal of Experimental Surgery
基金 国家自然科学基金资助项目(81171653、30950022、30972703) 江苏省科技型企业技术创新基金资助项目(BC2012093) 江苏省“333工程”科研项目资助项目(BRA2013054) 江苏省卫生厅医学科研招标立项课题(H201350) 常州市社会发展计划基金资助项目(CE20125017、CE20135048)
关键词 胃癌 B7-H4 CD11C 细胞因子诱导的杀伤细胞 Gastric cancer B7 -H4 CD11c Cytokine induced killer cells
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参考文献4

  • 1Shi L, Zhou Q, Wu J, et al. Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer [ J ]. Cancer Immunol Immunother,2012,61 ( 12 ) :2251-2259.
  • 2Choi IH,Zhu G, Sica GL, et al. Genomic organization and expression analysis of B7-H4, an immune inhibitory molecule of the B7 family [ J]. J Immunol,2003,171 (9) :4650-4654.
  • 3Dangaj D, Lanitis E, Zhao A, et al. Novel recombinant human bT-h4 antibodies overcome tumoral immune escape to potentiate T-cell anti- tumor responses[ J]. Cancer Res ,2013,73 ( 15 ) :4820-4829.
  • 4朱大伟,陈俊俊,裴红蕾.不同分期的胃癌患者组织中CD11c差异表达的研究[J].中华实验外科杂志,2013,30(5):1045-1047. 被引量:3

二级参考文献11

  • 1Takenaka S, McCormick S, Safroneeva E ,et al. Influence of the tissuemicroenvironment on Toll-like receptor expression by CD11 c + anti-gen-presenting cells isolated from mucosal tissues. Clin Vaccine Im-munol,2009 ,16 : 1615-1623.
  • 2Bachem A,Guttler S,Hartung E,et al. Superior antigen cross-presen-tation and XCR1 expression define human CD] lc + CD141 + cells ashomologues of mouse CD8 + dendritic cells. J Exp Med, 2010, 207 :1273-1281.
  • 3Pages F,Berger A,Camus M,et al. Effector memory T cells,early me-tastasis ,and survival in colorectal cancer. N Engl J Med,2005 ,353 :2654-2666.
  • 4Fahlen-Yrlid L, Gustafsson T, Westlund J, et al. CD1 1 c( high ) den-dritic cells are essential for activation of CD4 + T cells and generationof specific antibodies following mucosal immunization. J Immunol,2009,183:5032-5041.
  • 5Duan XZ,Zhuang H, Wang M,et al. Decreased numbers and impairedfunction of circulating dendritic cell subsets in patients with chronichepatitis B infection ( R2 ). J Gastroenterol Hepatol f 2005 , 20 : 234-242.
  • 6Shankaran V, Ikeda H, Bruce AT, et al. IFNgamma and lymphocytesprevent primary tumour development and shape tumour immunogenici -ty. Nature,2001 ,410; 1107-1111.
  • 7Street SE,Trapani JA,MacGregor D, et al. Suppression of lymphomaand epithelial malignancies effected by interferon gamma. J Exp Med,2002,196;129-134.
  • 8Vinay DS, Kwon BS. GDI 1 c + CD8 + T cells: two-faced adaptive im-mune regulators. Cell Immunol ,2010,264 : 18-22.
  • 9刘书漫,孟青,张钦宪,王盛典,刘占举,张谢夫.B7-H1及其受体PD-1在胃癌组织中的表达与意义[J].中华肿瘤杂志,2008,30(3):192-195. 被引量:23
  • 10蒋敬庭,吴昌平,沈月平,朱一蓓,陈陆俊,孙静,胡文蔚,孔炯,吴鸿雅,Lu Binfeng,张学光.共刺激分子B7-H4在胃癌组织中表达及其与预后的关系[J].中华实验外科杂志,2009,26(9):1155-1158. 被引量:29

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