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T细胞共刺激分子及其亚群在胃癌和大肠癌组织中表达的意义 被引量:6

Expression of T Cell Costimulatory Molecule and Variance of T Cell Subpopulations in Patients with Gastric Cancer and Colorectal Cancer
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摘要 目的探讨T细胞共刺激分子及其亚群在胃癌、大肠癌发生及预后中的作用。方法应用流式细胞术检测38例胃癌、42例大肠癌患者和21例健康人(对照组)外周血T细胞亚群及其共刺激分子CD28的表达。结果T细胞共刺激分子CD28(CD28+CD3+)表达:胃癌组为(25.80±10.56)%,大肠癌组为(28.95±9.29)%,均明显高于对照组的(0.82±0.98)%,P<0.01;总T细胞(CD3+)表达:胃癌组为(53.61±13.84)%,大肠癌组为(55.96±10.68)%,均明显低于对照组的(72.07±7.83)%,P<0.01;CD4+T细胞(CD4+CD3+)表达:胃癌组为(29.84±9.71)%,大肠癌组为(33.75±9.04)%,也均明显低于对照组的(38.79±5.08)%,P<0.01,P<0.05;细胞毒T细胞(CTL,CD8+CD28+CD3+)表达:胃癌组为(1.57±1.99)%,大肠癌组为(1.93±2.61)%,均明显高于对照组的(0.02±0.04)%,P<0.01;胃癌组CD8+抑制性T细胞(CD8+CD28-CD3+)和CD4/CD8比值明显低于对照组〔(16.06±6.94)%vs(20.56±6.54)%,P<0.05;(1.10±0.51)%vs(1.36±0.31)%,P<0.05〕;大肠癌组调节性T细胞(CD4+CD25+CD3+)明显高于对照组〔(19.74±6.89)%vs(13.72±3.08)%,P<0.01〕。胃癌组和大肠癌组患者手术前和手术后1周外周血T细胞亚群(除外胃癌组的CD3+细胞和CD28+CD3-细胞)的差异无统计学意义(P>0.05)。结论胃癌和大肠癌患者T细胞数量明显减少,T细胞共刺激分子CD28表达增高。胃癌患者CD4+T细胞显著减少;大肠癌患者调节性T细胞显著增加。 Objective To investigate the role of expression of T cell costimulatory molecule CD28 and variance of T cell subpopulations in the development and prognosis of gastric cancer and colorectal cancer. Methods The peripheral blood lymphocytes were tested for T cell subpopulations and T cell costimulatory molecule CD28 by flow cytometry in 38 patients with gastric cancer, 42 patients with colorectal cancer, and 21 healthy peoples as control group. Results Expressions of T cell costimulatory molecule CD28 in patients with gastric cancer and colorectal cancer were (25.80±10.56) % and (28.95±9.29) %, and significantly higher than that of control group [(0.82_±0.98) %, P〈0. 013. Expression percentage of total T cell (CD3+) in patients with gastric cancer and colorectal cancer were significantly lower than that of control group [ (53.61±13.84) % and (55.96 ± 10.68)% vs (72.07 ± 7.83) %, P〈0. 013. Expression percentage of CD4+ T cell (CD4+ CD3+ ) in patients with gastric cancer and colorectal cancer were significantly lower than that of control group [(29. 84 ± 9. 71) % and (33. 75 ± 9. 04) % vs (38.79±5.08) %; P〈0.01, P〈0. 053 ] Expression percentage of CTL cell (CD8+ CD28+ CD3+ ) in patients with gastric cancer and colorectal cancer were significantly higher than that of control group [(1. 57±1. 99)% and (1.93±2.61) % vs (0.02-1-0.04) % ; P〈0. 013 ] Expression percentage of CD8+ inhibitory T cell (CD8+ CD28- CD 3+) and CD4/CD8 ratio in patients with gastric cancer were significantly lower than that of control group[(16.06±6.94)% vs (20.56±6.54)%, P〈0.05; (1. 10±0.51)% vs (1.36±0.31)%, P〈0.05]; Expression of regulatory T cell (CD4+CD25+ CD3+) of patients with colorectal cancer was (19. 74± 6. 89)%, which was slgnificantly higher than that of control group [ ( 13.72 ± 3.08) %, P〈0.01]. No difference of expression was found in peripheral T cell subpopulations of postoperative patients with gastric cancer and colorectal cancer after one week (P〉0.05). Conclusion T cell number is [all, and T cell costimulatory molecule CD28 useless expression is increase in patients with gastric cancer and colorectal cancer. CD4+ T cell subpopulation is significantly de±creased in patients with gastric cancer. The regulatory T cell of patients with colorectal cancer is significantly increased.
出处 《中国普外基础与临床杂志》 CAS 2008年第1期51-55,共5页 Chinese Journal of Bases and Clinics In General Surgery
基金 福建省教育厅基金资助项目(编号:JB05245)~~
关键词 胃癌 大肠癌 共刺激分子 T细胞亚群 流式细胞术 Gastric cancer Colorectal cancer Costimulatory molecule T cell subpopulations Flow cytometry
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  • 1Antony PA, Piccirillo CA, Akpinarli A, et al CD8^+ T cell immunity against a tumor/self-antigen is augmented by CD4^+ T helper cells and hindered by naturally occurring T regulatory cells [J]. J Immunol, 2005; 174(5) : 2591
  • 2林学颜,张玲主编.现代细胞分子免疫学[M].第1版.北京;科学出版社,2003:384-385
  • 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
  • 4Chattopadhyay S, Chakraborty NG, Mukherji B. Regulatory T cells and tumor immunity [J]. Cancer Immunol Immunother, 2005; 54(12):1153
  • 5吴静静,王俐,张林杰.CD4^+CD25^+调节性T细胞及其与肿瘤的关系[J].国外医学(肿瘤学分册),2004,31(7):496-498. 被引量:6
  • 6李晓,汪辉.CD4^+CD25^+调节性T细胞和肿瘤免疫[J].国外医学(免疫学分册),2003,26(6):326-329. 被引量:10
  • 7Yu P, Lee Y, Liu W, etal. Intratumor depletion of CD4^+ cells unmasks tumor immunogenicity leading to the rejection of latestage tumors [J]. J Exp Med, 2005; 201(5) : 779
  • 8Seo N, Hayakawa S, Takigawa M, et al. Interleukin-10 expressed at early tumour sites induces subsequent generation of CD4^(+) T-regulatory cells and systemic collapse of antitumour immunity [J]. Immunology, 2001; 103(4) : 449
  • 9刘莉,丁乾,姚军霞,黄士昂.结直肠癌患者外周血CD4^+CD25^(high)调节性T细胞分析[J].中华肿瘤防治杂志,2007,14(2):110-113. 被引量:10
  • 10任秀红,刘莉,刘平平,董文川.恶性肿瘤患者T细胞亚群变化及其与肿瘤分期的关系[J].第三军医大学学报,2006,28(18):1906-1908. 被引量:38

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