Liver Cancer
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jan 1, 2004; 10(1): 53-57
Published online Jan 1, 2004. doi: 10.3748/wjg.v10.i1.53
Superantigen-SEA gene modified tumor vaccine for hepatocellular carcinoma: An in vitro study
Shao-Ying Lu, Yan-Fang Sui, Zeng-Shan Li, Jing Ye, Hai-Long Dong, Ping Qu, Xiu-Min Zhang, Wen-Yong Wang, Yu-Song Li
Shao-Ying Lu, Yan-Fang Sui, Zeng-Shan Li, Jing Ye, Hai-Long Dong, Ping Qu, Xiu-Min Zhang, Wen-Yong Wang, Yu-Song Li, Department of Pathology, Fourth Military Medical University, Xi’an 710032, Shaanxi Province, China
Shao-Ying Lu, Ph.D. Candidate of Xi’an Jiaotong University
Author contributions: All authors contributed equally to the work.
Supported by National Natural Science Foundation of China, No. 30271474 and No. 39770827
Correspondence to: Yan-Fang Sui, Professor, Department of Pathology, Fourth Military Medical University, Xi’an 710032, China. suiyanf@fmmu.edu.cn
Telephone: +86-29-3374541-211 Fax: +86-29-3374597
Received: May 13, 2003
Revised: May 20, 2003
Accepted: June 12, 2003
Published online: January 1, 2004
Abstract

AIM: To construct an eukaryotic superantigen gene expression vector containing the recombinant gene of SEA and CD80 molecule transmembrane region (CD80TM), and to express staphylococcus enterotoxin A (SEA) on the membrane of hepatocellular carcinoma (HCC) cell to form a superantigen gene modified tumor vaccine for HCC.

METHODS: SEA and linker-CD80TM gene were amplified through PCR from plasmid containing cDNA of SEA and CD80. Gene fragments were then subcloned into the multiple cloning sites of retroviral vector pLXSN. Recombinant plasmid was transferred into HepG2 cells mediated with lipofectamine, positive clones were selected in culture medium containing G418. RT-PCR and indirect immunofluorescence studies confirmed that SEA was expressed specifically on HCC cell membrane. INFγ -ELISPOT study demonstrated that SEA protein was expressed on the membrane of HCC cells. Cytotoxicity of HepG2-SEA primed CTLs (SEA-T) was analyzed by 51Cr release assay. T cells cultured with rhIL-2 (IL-2-T) were used as control.

RESULTS: Restriction digestion and sequence analyses confirmed the correctness of length, position and orientation of inserted fusion genes. SEA was expressed on the surface of HepG2 cells, HepG2-SEA had strong stimulating effect on production of HepG2 specific CTL (P < 0.001). SEA-T had enhanced cytotoxicity to HepG2 cells (P < 0.05).

CONCLUSION: Tumor cell membrane expressed superantigen can be used to reinforce the immune effect of tumor cell vaccine for HCC, which provides a new method of the enhanced active immunotherapy for HCC.

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