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商小英

作品数:4 被引量:11H指数:2
供职机构:北京大学基础医学院免疫学系更多>>
发文基金:北京市自然科学基金国家重点基础研究发展计划更多>>
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肝癌患者外周血CD8<'+>T细胞对HLA-A2限制性抗原肽NY-ESO-1p157-165及MAGE-3p271-279的免疫应答分析
该研究旨在探讨肝癌患者对来源于MAGE-3及NY-ESO-1基因的HLA<'->A2限制性抗原肽MAGE-3p271-279和NY-ESO-1p157-165的CD8<'+>T细胞的免疫应答能力,以判断其用作免疫治疗的可...
商小英
关键词:睾丸抗原抗原肽免疫应答酶联免疫斑点试验
用酶联免疫斑点法检测肝癌患者抗原特异性免疫应答能力被引量:4
2001年
目的 研究HLA A2阳性肝细胞癌 (HCC)患者及正常人外周血CD8+T细胞对流感病毒抗原肽 (Flup58 66)的免疫应答能力。方法 用免疫磁珠法分离出HCC患者与正常人外周血CD8+T细胞 ,以照射后自体CD8- 外周血单个核细胞 (PBMC)或树突状细胞 (DC)作为抗原提呈细胞 (APC) ,加载Flu抗原肽 ,经 7d培养诱导 ,用酶联免疫斑点 (ELISPOT)法检测诱导后产生γ干扰素的效应CD8+T细胞频数。结果 当效应细胞为 5× 1 0 4个 /孔时 ,CD8- PBMC作为APC ,Flu抗原肽特异的CD8+T细胞频数在HCC患者组 (n =8)为 2 2个± 9个 /孔 ,正常人组 (n =1 2 )为 59个± 2 7个 /孔 ,两组间差异有非常显著意义 (P <0 0 1 ) ,但均为阳性应答 ;在 5名正常人 ,Flu抗原特异的CD8+T细胞频数以DC为APC时高于以CD8- PBMC为APC时 (P <0 0 5)。结论 HCC患者对Flup58 66的免疫应答程度虽较正常人低 ,但大多数中晚期HCC患者仍然具有对抗原肽产生特异免疫应答的能力。
庞学雯商小英吕建峰彭吉润张华刚冷希圣陈慰峰
关键词:肝细胞癌抗原
酶联免疫斑点法检测抗原特异的CTL免疫应答试验条件的优化被引量:2
2002年
目的 探讨影响酶联免疫斑点 (ELISPOT)实验特异性及敏感性的因素 ,优化酶联免疫斑点法检测抗原特异的CTL免疫应答的实验条件。方法 HLA A2阳性正常人的外周血单个核细胞在体外经流感病毒抗原肽诱导 1周后 ,观察不同实验条件对酶联免疫斑点法检测抗原特异的CTL免疫应答的影响。结果 CTL诱导时 ,效应细胞先分离出CD8+ T细胞组获得的Flu抗原特异的细胞频数要高于CTL诱导后再分离出CD8+ T细胞组 (P <0 .0 5 ) ;自体DC(树突状细胞 )作APC(抗原提呈细胞 )比自体CD8- PBMC作APC ,CTL的诱导效率高且特异 (P <0 .0 5 ) ;使用细胞因子组合 (IL 7+IL 2 +IL 6 )优于单纯使用IL 2。CTL行ELISPOT检测时 ,T2 2细胞较T2 1细胞具有更强抗原提呈功能 ,增加Flu抗原特异的CD8+ T细胞频数 (P <0 .0 5 )。结论 优化了酶联免疫斑点法检测抗原特异的CTL免疫应答的试验条件 。
商小英庞学雯张华刚陈慰峰
关键词:酶联免疫斑点法抗原免疫应答
Induction of cytotoxic T lymphocytes from the peripheral blood of a hepatocellular carcinoma patient using melanoma antigen-1 (MAGE-1) peptide被引量:5
2002年
OBJECTIVE: To investigate the possibility of using melanoma antigen-1 (MAGE-1) peptide as a tumor vaccine to treat hepatocellular carcinoma (HCC). METHODS: The expressions of MAGE-1 in 8 HCC cell lines and in liver cancer tissue from a patient were detected using RT-PCR. The type of human leucocyte antigen I(HLA I) of both 8 HCC cell lines and peripheral blood mononuclear cells of the patient was detected using a microcytotoxicity method to screen out target cell lines for the cytotoxicity assay. Peripheral blood mononuclear cells from the HCC patient pulsed with an MAGE-1 peptide (NYKCRFPEI) were used as antigen presenting cells. Autogenous peripheral blood mononuclear cells were stimulated with antigen presenting cells every 7 days for 4 times to elicit cytotoxic T lymphocytes. The phenotype of effector cells was analyzed using flow cytometry. The cytotoxicity of effector cells was detected with a lactate dehydrogenase releasing assay. RESULTS: The expressions of both MAGE-1 and HLA-A24 were detected in BEL7405 cell line which were used as the positive target cell line in the cytotoxicity assay. The expression of MAGE-1 alone was detected in HLE, BEL7402, BEL7404, QGY7703 and SMMC7721 cell lines, and the expression of neither MAGE-1 nor HLA-A24 was shown in QGY 7701 and HpG2 cell lines. The last 7 cell lines could be used as negative target cell lines in the cytotoxicity assay. Peripheral blood mononuclear cells expanded 32 folds during 28-day culture. The ratio of CD3(+) T cells increased by 16% (from 54% to 70%), and the ratio of CD8(+) T cells increased by 20% (from 36% to 56%) during 28-day culture. When the ratio of effector cells to target cells was 10:1, effector cells exhibited 62.5% cytotoxicity against autogenous lymphoblasts pulsed with the peptide (NYKCRFPEI) of MAGE-1 antigen, 40.25% cytotoxicity against BEL7405 cells, compared with 17.88% cytolysis observed against autogenous lymphoblasts, 19.55% against HLE cells, and 1.6% against QGY7701 cells. When the ratio of effector cells to target cells wa
吕建锋冷希圣彭吉润牟东成庞学雯商小英陈慰峰
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