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Antitumor activities of human dendritic cells derived from peripheral and cord blood

查看全文 作　　者：Jin-Kun Zhang Jun Li Hai-Bin Chen Jin-Lun Sun Yao-Juan Qu Juan-Juan Lu Cancer Pathology Laboratory,Shantou University,Medical College,Shantou 515031,Guangdong Province,China 高影响力作者 出　　处：《World Journal of Gastroenterology》索引2002年第8卷第1期,共4页高影响力期刊 基　　金：Natural Science Foundation of the Higher Education Office of Guangdong Province,No.9501 and No.9816 摘　　要：AIM: To observe the biological specialization of humanperipheral blood dendritic cells (DC) and cord blood derivedDC and its effects on effector cells killing humanhepatocarcinoma cell line BEL-7402 in vitro.METHODS: The DC biological characteristics were detectedwith immunohistochemical and MTT assay. Two antitumorexperimental groups are: peripheral blood DC and cordblood DC groups. Peripheral blood DC groups used LAKcells as the effector cells and BEL-7402 as target cells, whilecord blood DC groups used CTL induced by tumor antigentwice pulsed DC as effector cells and BEL-7402 as targetcells, additional peripheral blood DC and cord blood DC areadded to observe its stimulating activities to effector cells.The effector's cytotoxicity to tumor cells were detected withneutral red colorimetric assay at two effector/target ratios of5:1 and 10: 1.RESULTS: Peripheral blood DC and cord blood DC highlyexpressed HLA-ABC, HLA-DR, HLA-DQ, CD54 and S-100protein. The stimulating activities to lymphocyteproliferation were compared between experimental groups(DC added) and control group (no DC added). In sixexperiment subgroups, the DC/lymphocyte ratio wassequentially 0.25: 100, 0.5: 100, 1: 100, 2: 100, 4: 100 and 8:100, A values(x± s) were 0.75396± 0.009, 0.84916± 0.010,0.90894± 0.012, 0.98371 ± 0.007, 1.01299 ± 0.006 and 1.20384± 0.006 in peripheral blood DC groups and 0.77650 ± 0.005,0.83008± 0.007, 0.92725 ± 0.007, 1.05990 ± 0.010, 1.15583 ±0.011, 1.22983 ± 0.011 in cord blood DC groups. A value was0.59517 ± 0.005 in control group. The stimulating activitieswere higher in experimental groups than in control group ( P< 0.01 ), which were increased when the DC concentrationwas enlarged ( P < 0.01 ). Two differently derived DCs hadthe same phenotypes and similar stimulating activities ( P >0.05). In peripheral blood DC groups, the cytotoxicity (x ±s) of the LD groups (experimental groups) and L groups(control group) was 58.16% ± 2.03% (5: 1), 46.18% ±2.25% (10:l) and 38.13% ± 1.29% (5: 1) and 65.40% ±1.56% (10: 1), respectively; in cord blood DC groups, TDgroups (experimental groups ) and T groups (controlgroups) were 69.71% ± 2.33% (5: 1 ), 77.64% ± 1.94% ( 10:1) a. nd 56.89% ± 1.82% (5:1) and 60.99% ± 1.42% (10:1),respectively. The cytotoxicity activities were enhanced withincreased effector/target ratio ( P < 0.01 ). At the sameeffector/target ratio, the cytotoxicity of experimental groupswas higher than that of control groups ( P < 0.01 ). Thecytotoxicity of cord blood DC groups were higher than ofperipheral blood DC groups ( P < 0.01 ).CONCLUSION: Peripheral blood DC and cord blood DC aremature DCs in morphology and function, both can enhancethe effector cell killing activities to hepetocarcinoma cells.DC pulsed with tumor antigen can induce ligher specific CTLactivity than unpulsed DC. 关 键 词：肝癌 树突状细胞 抗肿瘤机制 外周血 脐带血
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