Esophageal Cancer
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Apr 1, 2004; 10(7): 934-939
Published online Apr 1, 2004. doi: 10.3748/wjg.v10.i7.934
Study on immune function of dendritic cells in patients with esophageal carcinoma
Shen-Ren Chen, Yi-Ping Luo, Jin-Kun Zhang, Wei Yang, Zhi-Chao Zhen, Lin-Xin Chen, Wei Zhang
Shen-Ren Chen, Yi-Ping Luo, Wei Yang, Zhi-Chao Zhen, Lin-Xin Chen, Wei Zhang, The Second University Hospital, Shantou University Medical College, Shantou 515041, Guangdong Province, China
Jin-Kun Zhang, 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. 0144
Correspondence to: Professor Shen-Ren Chen, The Second University Hospital of Shantou University Medical College, Dongsha Northern Road, Shantou 515041, Guangdong Province, China. chen-shenren@163.com
Telephone: +86-754-8355431 Fax: +86-754-8346543
Received: August 23, 2003
Revised: September 17, 2003
Accepted: October 22, 2003
Published online: April 1, 2004
Abstract

AIM: To investigate the immune function of dendritic cells from both peripheral blood and operated tissues of esophageal carcinoma patients in order to find the relationship between the immune function of dendritic cells and the pathogenesis of esophageal carcinoma.

METHODS: The expression of CD83, CD80, and CD86 on the surface of dendritic cells cultured from the peripheral blood of patients was detected compared with that from health donors using flow cytometry. The ability of dendritic cells to induce T lymphocyte proliferation was evaluated by a liquid scintillation counter. The expression of CD80, CD86, CD83, and S-100 proteins was assessed in esophageal carcinoma tissues using immunohistochemical method.

RESULTS: Compared with those from healthy donors, dendirtic cells cultured from the peripheral blood of patients expressed lower CD80 and CD86. Furthermore, the ability of dendritic cells in patients to induce T lymphocyte proliferation was significantly lower than that of the control group. Compared with the control group, the positive expression ratio and frequencies of CD80, CD86, and S-100 in esophageal carcinoma tissues were significantly down regulated. The expression of CD83 was up-regulated in the pericancerous tissues, but no expression was found in the cancerous nodules.

CONCLUSION: The impaired immune function and the decreased number of dendritic cells cause pathogenesis and progression of esophageal carcinoma.

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