Author(s): Yiang, GT (Yiang, Giou-Teng); Harn, HJ (Harn, Horng-Jyh); Yu, YL (Yu, Yung- Luen); Hu, SC (Hu, Sheng-Chuan); Hung, YT (Hung, Yu-Ting); Hsieh, CJ (Hsieh, Chia-Jung);
Lin, SZ (Lin, Shinn-Zong); Wei, CW (Wei, Chyou-Wei)
Title: Immunotherapy: rAAV2 expressing interleukin-15 inhibits HeLa cell tumor growth in mice
Source: JOURNAL OF BIOMEDICAL SCIENCE, 16: Art. No. 47 MAY 7 2009 Language: English
Document Type: Article
KeyWords Plus: RECOMBINANT ADENOASSOCIATED VIRUS; DIRECTED GENE- THERAPY; CANCER A549 CELLS; IN-VIVO; EFFICIENT TRANSDUCTION; TRANSGENE EXPRESSION; IMMUNOGENE THERAPY; IMMUNE-RESPONSE; DENDRITIC CELLS;
PROTEIN-KINASE
Abstract: Human interleukin-15 (hIL15) has anti-tumor activities, but it is not convenient for tumor treatment because of its short half-life. A gene therapy for mouse lung cancer using an adenovirus vector expressing IL15 has been reported. However, adenovirus vector-mediated gene therapy can provoke cellular toxicity and inflammatory reactions. The recombinant adenovirus-associated vector 2 (rAAV2) is safer due to minimal cellular toxicity and immune response. In order to demonstrate that gene therapy can be used safely and successfully for human cancer treatment, the rAAV2 expressing hIL15 gene (rAAV2-hIL15) is applied for human cervical cancer, HeLa cell, in this study. This study successfully demonstrates that rAAV2-hIL15 can express IL15 with bioactivities in vitro and in vivo. In conclusion, our studies show that human cervical cancers are inhibited on animal model with rAAV2-hIL15 treatment and provide a safer and important reference for human cancer gene therapy.
Addresses: [Lin, Shinn-Zong] China Med Univ Hosp, Dept Neurosurg, Taichung, Taiwan;
[Yiang, Giou-Teng; Hu, Sheng-Chuan] Tzu Chi Univ, Inst Med Sci, Hualien, Taiwan; [Yiang, Giou-Teng; Hu, Sheng-Chuan] Tzu Chi Gen Hosp, Dept Emergency Med, Hualien, Taiwan;
[Harn, Horng-Jyh] China Med Univ Hosp, Dept Pathol, Taichung, Taiwan; [Yu, Yung-Luen]
China Med Univ & Hosp, Grad Inst Canc Biol, Taichung, Taiwan; [Yu, Yung-Luen] China Med Univ & Hosp, Ctr Mol Med, Taichung, Taiwan; [Yu, Yung-Luen] Asia Univ, Dept Biotechnol, Taichung, Taiwan; [Hung, Yu-Ting; Hsieh, Chia-Jung; Wei, Chyou-Wei] Hung Kuang Univ, Coll Med & Nursing, Inst Biomed Nutr, Taichung, Taiwan
Reprint Address: Lin, SZ, China Med Univ Hosp, Dept Neurosurg, Taichung, Taiwan.
E-mail Address: [email protected]; [email protected];
[email protected]; [email protected]; [email protected];
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Publisher: BIOMED CENTRAL LTD
Publisher Address: CURRENT SCIENCE GROUP, MIDDLESEX HOUSE, 34-42 CLEVELAND ST, LONDON W1T 4LB, ENGLAND
ISSN: 1021-7770 Article Number: 47
DOI: 10.1186/1423-0127-16-47
29-char Source Abbrev.: J BIOMED SCI ISO Source Abbrev.: J. Biomed. Sci.
Source Item Page Count: 8
Subject Category: Medicine, Research & Experimental ISI Document Delivery No.: 460EW