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HLA-A2限制性NY-ESO-1b肽段诱导的CD8+ T细胞对稳定表达NY-ESO-1的HepG2肝癌细胞系的杀伤效应
引用本文:乔欢,钱晓萍,张华刚,田婵,陈慰峰.HLA-A2限制性NY-ESO-1b肽段诱导的CD8+ T细胞对稳定表达NY-ESO-1的HepG2肝癌细胞系的杀伤效应[J].北京大学学报(医学版),2005,37(6):565-568.
作者姓名:乔欢  钱晓萍  张华刚  田婵  陈慰峰
作者单位:北京大学医学部基础医学院免疫学系T细胞室,北京,100083;北京大学医学部基础医学院免疫学系T细胞室,北京,100083;北京大学医学部基础医学院免疫学系T细胞室,北京,100083;北京大学医学部基础医学院免疫学系T细胞室,北京,100083;北京大学医学部基础医学院免疫学系T细胞室,北京,100083
基金项目:科技部科研项目 , 北京市自然科学基金 , 国家科技攻关项目
摘    要:目的:分析体外诱导的NY-ESO-1特异性杀伤性T淋巴细胞对稳定表达NY-ESO-1蛋白的肝细胞性肝癌(hepatocellular carcinoma,HCC)细胞系的杀伤效应,为进一步分析NY-ESO-1蛋白作为疫苗用于治疗HCC的可能性提供实验支持.方法:从HLA-A2阳性的肝癌患者体内分离出外周血单个核细胞,用NY-ESO-1肽段体外诱导特异性杀伤性T淋巴细胞,并通过酶联免疫斑点法分析特异性杀伤性T淋巴细胞对稳定表达NY-ESO-1蛋白的HCC细胞系HepG2细胞的杀伤效应.结果:转染了NY-ESO-1的HepG2细胞(HLA-A2 )可有效地被NY-ESO-1157-165抗原肽诱导的特异性CD8 T淋巴细胞所识别.效应细胞中大量GrB的释放表明其对稳定转染了NY-ESO-1基因的HepG2细胞有很强的杀伤作用.结论:HepG2细胞中表达的NY-ESO-1蛋白可被此肝癌细胞有效地加工处理,而且HLA-A2限制性的抗原肽NY-ESO-1157-165也可被有效地提呈到细胞表面,从而被效应T细胞所识别.

关 键 词:  肝细胞  抗原  肿瘤  肿瘤细胞  培养的  酶联免疫吸附测定
文章编号:1671-167X(02005)06-0565-04
修稿时间:2005年5月11日

Estimation of an NY-ESO-1 expressing HCC cell line by NY-ESO-1b specific CD8+T cells in vitro induced by HLA-A2 restricted NY-ESO-1b peptide
QIAO Huan,QIAN Xiao-ping,ZHANG Hua-gang,TIAN Chan,CHEN Wei-feng.Estimation of an NY-ESO-1 expressing HCC cell line by NY-ESO-1b specific CD8+T cells in vitro induced by HLA-A2 restricted NY-ESO-1b peptide[J].Journal of Peking University:Health Sciences,2005,37(6):565-568.
Authors:QIAO Huan  QIAN Xiao-ping  ZHANG Hua-gang  TIAN Chan  CHEN Wei-feng
Affiliation:T Cell Laboratory of Department of Immunology, Peking University School of Basic Medical Science, Beijing 100083, China.
Abstract:OBJECTIVE: To analyze the effect of an NY-ESO-1 expressing HCC cell line by NY-ESO-1b specific CD8(+)T cells in vitro induced by HLA-A2 Restricted NY-ESO-1b peptide and to further analyze the possibility of NYjESOj1 as a vaccine in HCC treatment. METHODS: Peripheral blood mononuclear cells (PBMCs) were obtained from an HLA-A2(+) HCC patient and NY-ESO-1 specific CD8(+)T cells were in vitro induced by HLA-A2 Restricted NY-ESO-1b peptide. Next we estimated the effect that NY-ESO-1 specific CD8(+)T cells recognized and killed NY-ESO-1 expressing HepG2 cells by enzyme-linked immunospot(ELISPOT). RESULTS: These in vitro induced NY-ESO-1b specific CD8(+)T cells could recognize HepG2 cells stably transfected with NY-ESO-1 in both IFN-gamma and Granzyme B ELISPOT assays. And the data also showed that NY-ESO-1 specific CD8(+)T cells could efficiently kill NY-ESO-1 expressing HepG2 cells. CONCLUSION: NY-ESO-1 protein can be processed by HCC cells, and that HLA-A2 restricted NY-ESO-1b peptide (157-165) can also be presented on the surfaces of cells and recognized by NY-ESO-1b specific CD8(+)T cells in vitro induced.
Keywords:Carcinoma  hepatocellular  Antigens  neoplasm  Tumor cells  cultured  Enzyme-linked immunosorbent assay
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