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胃癌患者PBMCs中CD4+CD25+T细胞体外增殖及对CD4+CD25-T细胞增殖的影响
引用本文:王凌云,陈梅,朱兆华,彭辉,吴长有. 胃癌患者PBMCs中CD4+CD25+T细胞体外增殖及对CD4+CD25-T细胞增殖的影响[J]. 中国病理生理杂志, 2006, 22(11): 2202-2206. DOI: 1000-4718
作者姓名:王凌云  陈梅  朱兆华  彭辉  吴长有
作者单位:中山大学附属第二医院 1 消化内科, 2 检验科, 广东 广州 510120;3 中山大学基础医学院免疫教研室, 广东 广州 510180
摘    要:目的:探讨胃癌患者外周血单个核细胞(PBMCs)中的CD4+CD25+T细胞体外增殖及对CD4+CD25-T细胞增殖的影响。 方法:以免疫磁性分离方法 (MACS)分选出胃癌患者外周血单个核细胞中的CD4+CD25+T及CD4+CD25-T细胞后,用流式细胞仪分析细胞的纯度及活力;再以小鼠抗人CD3单抗、小鼠抗人CD28单抗及rh IL-2作为共刺激因子,观察与CD4+CD25-T细胞共培养时,CD4+CD25+T细胞对CD4+CD25-T细胞增殖的抑制效应。 结果:(1)分选后健康对照组及胃癌患者PBMC 中CD4+CD25+ T细胞纯度分别为83.8%±1.84%、84.13%±2.77%,两者相比,无显著差异(P>0.05);(2)经MACS 分选后正常对照组与胃癌患者CD4+CD25+ T细胞活力分别为98.52%±0.72%、97.80%±0.95%,两者相比,无显著差异(P>0.05);(3)无论是健康对照还是胃癌患者的CD4+CD25+T均具有明显抑制效应性T细胞如CD4+CD25-T细胞的增殖,随着CD4+CD25+T细胞数的增加,这种抑制增殖的能力也相应增加,当CD4+CD25+∶〖KG-*2〗CD4+CD25-T达 1∶〖KG-*2〗1时,抑制率最大达到50%。 结论:MACS分选法能够分选出高纯度及活力的CD4+CD25+T细胞,分选后CD4+CD25+T细胞在体外均能抑制CD4+CD25-T细胞增殖,且这种抑制效应呈一定效靶比关系。

关 键 词:胃肿瘤  CD4+CD25+T细胞  CD4+CD25-T细胞  细胞增殖  
文章编号:1000-4718(2006)11-2202-05
收稿时间:2006-01-11
修稿时间:2006-01-112006-06-21

Proliferation of CD4+CD25+ T cells from PBMCs of the gastric cancer patients and inhibitory effect on CD4+CD25- T cells in vitro
WANG Ling-yun,CHEN Mei,ZHU Zhao-hua,PENG Hui,WU Chang-you. Proliferation of CD4+CD25+ T cells from PBMCs of the gastric cancer patients and inhibitory effect on CD4+CD25- T cells in vitro[J]. Chinese Journal of Pathophysiology, 2006, 22(11): 2202-2206. DOI: 1000-4718
Authors:WANG Ling-yun  CHEN Mei  ZHU Zhao-hua  PENG Hui  WU Chang-you
Affiliation:1Department of Gastroenterology, 2 Department of Laboratory Diagnosis, The Second Affiliated Hospital of Sun Yat-sen University, Guangzhou 510120, China. E-mail:zhuzhaohua@yahoo.com.cn;3 Department of Immunology, Sun Yat-sen University, Guangzhou 510080, China
Abstract:AIM:To investigate the proliferation of CD4+CD25+ T cells from PBMCs of the gastric cancer patients and the inhibitory effect on CD4+CD25- T cells in vitro. METHODS:Magnetic activated cell sorting (MACS) method was used to separate CD4+CD25+T and CD4+CD25-T cells from peripheral blood monocytic lymphocytes in the gastric cancer patients, and then the purity and activity of CD4+CD25+T cells were analyzed with flow cytometer. After stimulated with anti-CD3 Ab, anti-CD28 Ab and rh IL-2, CD4+CD25- and CD4+CD25+ T cells were cocultured. The inhibitory effect of CD4+CD25+T on CD4+CD25-T cells was assayed by [3H] thymidine proliferation experiment. RESULTS:(1)After sorting, CD4+CD25+ T cells purity in healthy control and gastric cancer patients were 83.80%±1.84% and 84.13%±2.77%, respectively. No significant difference between the two groups (P>0.05) was observed. (2)The activity of CD4+CD25+ and CD4+CD25- T cells in healthy control and the gastric cancer patients after sorting were 98.52%±0.72% and 97.80%±0.95%. There was no significantly difference between the two groups (P>0.05). (3) CD4+CD25+ T cells obviously inhibited the CD4+CD25-T cell proliferation in vitro. The inhibition achieved to maximum in coculture of CD4+CD25+ T cells together with CD4+CD25- T cells (ratio of 1∶〖KG-*2〗1). CONCLUSION:The MACS system can effectively isolate CD4+CD25+ and CD4+CD25- T cells. After sorting, CD4+CD25+T cells obviously inhibit the proliferation of CD4+CD25- T cells in vitro and the inhibitory effect display an effect-target ratio relationship.
Keywords:Stomach neoplasms  CD4~ CD25~ T cells  CD4~ CD25~-T cells  Cell proliferation
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