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不同刺激剂诱导肺癌患者引流淋巴结细胞分泌细胞因子的研究
引用本文:李启亮,单保恩,张超,何明,张正茂. 不同刺激剂诱导肺癌患者引流淋巴结细胞分泌细胞因子的研究[J]. 细胞与分子免疫学杂志, 2006, 22(5): 609-612
作者姓名:李启亮  单保恩  张超  何明  张正茂
作者单位:河北医科大学第四医院科研中心,河北,石家庄,050011
基金项目:国家人事部科研项目基金
摘    要:目的:探讨多种刺激剂对肿瘤引流淋巴结(TDLN)细胞分泌细胞因子的影响及其抗肿瘤效应和机制。方法:采用ELISA和Griess法测定不同刺激组(分别为IL2、IL2 自身肺癌细胞抗原、IL2 GMCSF IL4 自身肺癌细胞抗原和IL2 GMCSF IL4 LPS)刺激TDLN后第7、14、21天,分泌IL12p70、IFNγ、TNFα和NO的水平。结果:IL2 GMCSF IL4 自身肺癌细胞抗原和IL2 GMCSF IL4 LPS组刺激的TDLN细胞中,CD83 细胞的比率明显增多,分泌IL12p70、IFNγ及TNFα的水平也明显高于IL2和IL2 自身肺癌细胞抗原刺激组,IL2 GMCSF IL4 LPS组刺激的TDLN细胞分泌NO的水平明显高于其他3组。各种刺激剂刺激TDLN细胞后,分泌IL12p70、IFNγ和NO的水平在第14天时达到高峰。结论:不同刺激剂诱导TDLN细胞中的CD83 细胞数量不同,故具有不同的抗肿瘤活性。

关 键 词:肿瘤引流淋巴结细胞  细胞因子  抗肿瘤活性
文章编号:1007-8738(2006)05-0609-04
收稿时间:2005-08-22
修稿时间:2005-12-29

Study of cytokines secreted by tumor-draining lymph node cells from lung cancer patients induced with different stimulators
LI Qi-liang,SHAN Bao-en,ZHANG Chao,HE Ming,ZHANG Zheng-mao. Study of cytokines secreted by tumor-draining lymph node cells from lung cancer patients induced with different stimulators[J]. Chinese journal of cellular and molecular immunology, 2006, 22(5): 609-612
Authors:LI Qi-liang  SHAN Bao-en  ZHANG Chao  HE Ming  ZHANG Zheng-mao
Affiliation:esearch Center of the Fourth Affiliated Hospital, Hebei Medical University, Shijiazhuang 050011 , China
Abstract:AIM: To investigate the influence of different stimulators on cytokines secretion of tumor-draining lymph node (TDLN) cells and study antitumor effects and mechanism of TDLN cells. METHODS: IL-12 p70, IFN-gamma, TNF-alpha and NO which were secreted by TDLN cells induced by different stimulators (IL-2 group, IL-2+autologous tumor antigen group, IL-2+GM-CSF+IL-4+autologous tumor antigen group and IL-2+GM-CSF+IL-4+LPS group) were detected by ELISA and Griess after TDLN cells were stimulated for 7, 14 and 21 d. RESULTS: The rate of CD83(+) cells of TDLN cells induced by IL-2+GM-CSF+IL-4+autologous tumor antigen and IL-2+GM-CSF+IL-4+LPS was significantly increased. The TDLN cells in the two groups secreted much more IL-12 p70, IFN-gamma and TNF-alpha than IL-2 group and IL-2+autologous tumor antigen group. The TDLN cells stimulated by IL-2+GM-CSF+IL-4+LPS secreted significantly more NO than the other three groups. TDLN cells in each group secreted IL-12 p70, IFN-gamma and NO at the highest level after TDLN cells were stimulated for 14 d. CONCLUSION: Different stimulators can make TDLN cells produce different number of CD83(+) cells (DC), which gives TDLN cells different antitumor activity.
Keywords:NO
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