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肿瘤患者外周血中抑制性受体LAIR-1表达升高
引用本文:薛江楠,王春艳,张晓姝,曹奇志,宿振国.肿瘤患者外周血中抑制性受体LAIR-1表达升高[J].细胞与分子免疫学杂志,2008,24(4):373-375.
作者姓名:薛江楠  王春艳  张晓姝  曹奇志  宿振国
基金项目:山东省自然科学基金 , 山东省教育厅资助项目
摘    要:目的:研究LAIR-1在肿瘤患者中的表达,探讨其在抗肿瘤免疫应答中的作用.方法:应用夹心ELISA检测肿瘤患者血清中可溶型sLAIR-1的水平;应用免疫荧光染色和流式细胞术分析,观察LAIR-1在患者PBMC中NK细胞、CD4 T细胞、CD8 T细胞和B细胞上的表达.结果:肿瘤患者血清sLAIR-1水平为(4.6±3.2) μg/ L,明显高于正常人血清sLAIR-1 水平(3.9±3.0) μg/L,P<0.05.NK细胞,CD4 T细胞及CD8 T细胞表达LAIR-1水平上调.肺癌患者CD4/CD8比值明显低于正常人,B细胞百分率明显高于正常人.NK细胞、CD4 T细胞CD8 T细胞中LAIR-1的表达阳性率高于对照组.结论:在肿瘤患者LAIR-1分子表达水平高于正常人.肿瘤患者抑制性受体LAIR-1 表达水平的上调可能与肿瘤的免疫逃逸有关.

关 键 词:LAIR-1  CD305  抑制性受体  肿瘤  肿瘤患者  外周血  抑制性受体  表达水平  PBMC  patients  tumor  免疫逃逸  分子  对照组  表达阳性率  百分率  正常人血清  比值  癌患者  细胞表达  结果  流式细胞术分析  免疫荧光染色  可溶型
文章编号:1007-8738(2008)04-0373-03
修稿时间:2008年1月7日

The up-regulated expression of LAIR-1 in tumor patients PBMC
XUE Jiang-nan,WANG Chun-yan,ZHANG Xiao-shu,CAO Qi-zhi,SU Zhen-guo.The up-regulated expression of LAIR-1 in tumor patients PBMC[J].Journal of Cellular and Molecular Immunology,2008,24(4):373-375.
Authors:XUE Jiang-nan  WANG Chun-yan  ZHANG Xiao-shu  CAO Qi-zhi  SU Zhen-guo
Institution:Department of Immunology, Binzhou Medical University, Yantai 264003, China.
Abstract:AIM: To investigate the expression of LAIR-1 in patients with tumors and the function of LAIR-1 in anticancer immunity. METHODS: A sandwich ELISA was employed to detect the serum sLAIR-1 from tumor patients and healthy individuals. The expression of LAIR-1 in CD4(+) T cells, CD8(+) T cells, NK cells and B cells isolated from the peripheral blood of cancer patients was examined by fluorescence staining and flow cytometry. RESULTS: The level of serum sLAIR-1 in tumor patients was higher than that in heatlhy individuals 4.6+/-3.2 mug/L vs 3.9+/-3.0 mug/L, P<0.05]. NK cells, CD4(+) T cells and CD8(+) T cells expressed the up-regulated LAIR-1. The ratio of CD4/CD8 in lung cancer patients decreased significantly while the percentage of B cells in cancer patients increased greatly compared with healthy individuals. CONCLUSION: The expression of LAIR-1 is up-regulated in tumor patients, which may contribute to cancer immune escape.
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