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机构地区:[1]山西医科大学微生物与免疫教研室,太原030001
出 处:《肿瘤研究与临床》2009年第4期239-241,共3页Cancer Research and Clinic
基 金:基金项目:山西医科大学科技创新基金(01200712);山西医科大学博士启动基金(03200705)
摘 要:目的探讨肿瘤细胞是否能上调CD4+CD25+调节性T细胞(Treg细胞)的比例。方法将小鼠淋巴瘤细胞株EL4培养上清液与正常小鼠脾脏淋巴细胞混合培养72h,流式细胞仪检测其中CD4+CD25+Treg细胞含量,RT—PCR检测Foxp3mRNA的表达,实验重复3次。结果和EL-4培养上清液混合培养的正常小鼠脾脏淋巴细胞中CD4+CD25+Treg细胞的比例高于对照组(P〈0.05),在CD3单抗刺激的同时加入EL-4培养上清液后,小鼠脾脏中CD4+CD25+Treg细胞仍呈同步增加(P〈0.05);且Foxp3mRNA的表达增加。结论淋巴瘤细胞分泌的免疫调节因子能诱导CD4+CD25+Treg细胞的增生,提示肿瘤可以上调CD4+CD25+Treg细胞比例。Objective To explore if the tumor cell can up-regulate the proliferation ofCD4+CD25+ Treg cells. Methods Lymphoma cell EL-4 supernatant was combined with the normal mise spleen lymphocyte. After cultured 72 hours, CD4+CD25+ subset were analyzed by flow cytometry and the gene expression level of the specific marker Foxp3 were tested by RT-PCR. The experiment repeated three times. Results The supernatant derived from EL-4 can increase the proportion of CD4+CD25+ Treg ceils in normal mouse spleen lymphocytes than that of the control group. Moreover, when added the CD3 McAb with EL-d supernatant together, the number of CD4+CD25+ Treg cells increased. The level of corresponding Foxp3 mRNA also increased. Conclusion These data suggested that in the supematant may occur immune regulatory factors which up-regulated the number of CD4+CD25+ Treg cells and indicated that the tumorigenesis can facilitate proliferation of CD4+CD25+ Treg cells.
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