Liver Cancer
Copyright ©The Author(s) 2002. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 15, 2002; 8(1): 87-90
Published online Feb 15, 2002. doi: 10.3748/wjg.v8.i1.87
Antitumor activities of human dendritic cells derived from peripheral and cord blood
Jin-Kun Zhang, Jun Li, Hai-Bin Chen, Jin-Lun Sun, Yao-Juan Qu, Juan-Juan Lu
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
Author contributions: All authors contributed equally to the work.
Supported by Natural Science Foundation of the Higher Education Office of Guangdong Province, No. 9501 and No.9816
Correspondence to: Prof. Jin Kun Zhang, Cancer Pathology Laboratory, Shantou University Medical College, 22 Xinlinglu, Shantou 515031, Guangdong Province, China. Jkzhang@stu.edu.cn
Telephone: +86-754-8900443 Fax: +86-754-8557562
Received: July 19, 2001
Revised: December 11, 2001
Accepted: December 29, 2001
Published online: February 15, 2002
Abstract

AIM: To observe the biological specialization of human peripheral blood dendritic cells (DC) and cord blood derived DC and its effects on effector cells killing human hepatocarcinoma cell line BEL-7402 in vitro.

METHODS: The DC biological characteristics were detected with immunohistochemical and MTT assay. Two antitumor experimental groups are: peripheral blood DC and cord blood DC groups. Peripheral blood DC groups used LAK cells as the effector cells and BEL-7402 as target cells, while cord blood DC groups used CTL induced by tumor antigen twice pulsed DC as effector cells and BEL-7402 as target cells, additional peripheral blood DC and cord blood DC are added to observe its stimulating activities to effector cells. The effector¡äs cytotoxicity to tumor cells were detected with neutral red colorimetric assay at two effector/ target ratios of 5:1 and 10:1.

RESULTS: Peripheral blood DC and cord blood DC highly expressed HLA-ABC, HLA-DR, HLA-DQ, CD54 and S-100 protein. The stimulating activities to lymphocyte proliferation were compared between experimental groups (DC added) and control group (no DC added), in six experiment subgroups,the DC/lymphocyte ratio was sequentially 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 was 0.59517 ± 0.005 in control group. The stimulating activities were higher in experimental groups than in control group (P < 0.01), which were increased when the DC concentration was enlarged (P < 0.01). Two differently derived DCs had the 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), 46c18% ± 2.25% (10:1) and 38c13% ± 1.29% (5:1) and 65.40% ± 1.56% (10:1) respectively; in cord blood DC groups, TD groups (experimental groups) and T groups (control groups) were 69.71% ± 2.33% (5:1), 77.64% ± 1.94% (10:1) and 56.89% ± 1.82% (5:1) and 60.99% ± 1.42% (10:1) respectively. The cytotoxicity activities were enhanced with increased effector/target ratio (P < 0.01). At the same effector/target ratio, the cytotoxicity of experimental groups were bigger than that of control groups (P < 0.01). The cytotoxicity activities of cord blood DC groups were higher than that of peripheral blood DC groups (P < 0.01).

CONCLUSION: Peripheral blood DC and cord blood DC are mature DC in morphology and function, both can enhance the effector cell killing activities to hepatocarcinoma cells. DC pulsed with tumor antigen can induce higher specific CTL activity than unpulsed DC.

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