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CD4~+ CD25~+调节性T细胞在Lewis肺癌移植鼠中的检测及临床意义

The expression and clinical significance of CD4~+ CD25~+ Treg in mice with Lewis lung cancer

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【作者】 李欣崔永生王炎郑晓辉李一

【Author】 LI Xin1,CUI Yong-sheng1,2,WANG Yan1,ZHENG Xiao-hui1,LI Yi11Department of Immunology,School of Basic Medical Sciences,Jilin University,Changchun 130021,China;2Department of Thoracic Surgery,First Hospital,Jilin University,Changchun 130021,China.

【机构】 吉林大学白求恩医学部基础医学院免疫学教研室吉林大学白求恩医学部基础医学院免疫学教研室 吉林长春130021吉林长春130021吉林大学第一临床医院胸外科吉林长春130021

【摘要】 目的:研究Lewis肺癌移植鼠胸腺与脾脏CD4+ CD25+调节性T细胞数量及其相关基因Foxp3 mR-NA的表达特点,探讨CD4+ CD25+调节性T细胞在诱导肿瘤免疫耐受中的作用。方法:将传代培养的Lewis肺癌细胞接种于C57BL/6小鼠右腋皮下,建立Lewis肺癌模型。观测成瘤率、平均瘤重、肿瘤体积动态变化;采用MTT法检测胸腺及脾脏T淋巴细胞增殖功能;采用流式细胞术检测胸腺及脾脏CD4+ CD25+调节性T细胞数量变化;采用半定量RT-PCR方法检测肺癌小鼠胸腺与脾脏Foxp3 mRNA表达水平。结果:Lewis肺癌的移植成瘤率为100%,平均瘤重(3.34±1.79)g;胸腺T淋巴细胞增殖功能略有降低,但降低不显著(P>0.05),而脾脏T淋巴细胞增殖功能明显降低(P<0.05);胸腺及脾脏CD4+CD25+调节性T细胞数量均明显升高(P<0.05);Foxp3 mRNA在肺癌模型组的胸腺表达明显增高(P<0.05),在肺癌模型组脾脏Foxp3 mRNA表达中也略有增加,但增高不显著(P>0.05)。结论:CD4+CD25+调节性T细胞可能在肿瘤免疫耐受中发挥重要作用。

【Abstract】 Objective: To study the number of CD4+CD25+ Treg and the expression of Foxp3 mRNA in thymus and spleen in mice with Lewis lung cancer, and investigate the role of CD4+CD25+ Treg in tumor immunological tolerance. Methods: The models were established by injected subcutaneously to the right axilla of C57BL/6 mice with subculturing Lewis lung cancer cells. The rate of tumor forming, tumor weight, the dynamic change of tumor volume were observed. The changes of T lymphocyte proliferation in thymus and spleen were detected by MTT test .The changes of number of CD4+CD25+ Treg were detected by flow cytometer and the expression of Foxp3 in thymus and spleen were analyzed by semi-quantitative RT-PCR. Results: The rate of tumor forming was 100%, tumor weight was 3.34 1.79g. The changes of T lymphocyte proliferation in thymus was lower in the tumor mice than in the normal mice, but not significantly like in splenic lymphocytes(P>0.05). The changes of T lymphocyte proliferation in spleen was significantly lower in the tumor mice than in the normal mice(P<0.05). The number of CD4+CD25+ Treg in thymus and spleen of mice was markedly higher in the tumor mice than in the normal mice(P<0.05). The expression of Foxp3 mRNA in thymic lymphocyte was significantly higher in tumor mice (P<0.05).The expression of Foxp3 mRNA in splenic lymphocyte was also shown higher in tumor mice than normal mice, but not significantly like in thymic lymphocytes(P>0.05). Conclusion: CD4+CD25+regulatory T cell might be responsible for immune suppression in the tumor immunity and play it’s function in tumor tolerance.

【基金】 国家自然科学基金资助项目(30571724)
  • 【文献出处】 现代肿瘤医学 ,Journal of Modern Oncology , 编辑部邮箱 ,2007年04期
  • 【分类号】R734.2
  • 【被引频次】16
  • 【下载频次】405
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