Abstract |
Despite the recent improvement in the treatment of ovarian cancer, this disease is still leading cause of cancer death in women. In this study, the anti- tumor activity of cytokine-induced killer (CIK) cells against human ovarian cancer was evaluated in vitro and in vivo. Although CD3+CD56+ cells were rare in fresh human peripheral blood mononuclear cells, they could expand more than 1,000-fold on day 14 in the presence of anti-CD3 antibody plus IL-2. At an effector-target cell ratio of 30:1, CIK cells destroyed 45% of SK-OV-3 human ovarian cancer cells, which was determined by the 51Cr-release assay. In addition, CIK cells at a dose of 23 million cells per mouse inhibited 73% of SK-OV-3 tumor growth in nude mouse xenograft assay. This study suggests that CIK cells may be used as an adoptive immunotherapy for patients with ovarian cancer.
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Authors | Hwan Mook Kim, Jong Soon Kang, Jaeseung Lim, Song-Kyu Park, Kiho Lee, Yeo Dae Yoon, Chang Woo Lee, Ki Hoon Lee, Gyoonhee Han, Kyu-Hwan Yang, Yeon Jin Kim, Youngsoo Kim, Sang-Bae Han |
Journal | Archives of pharmacal research
(Arch Pharm Res)
Vol. 30
Issue 11
Pg. 1464-70
(Nov 2007)
ISSN: 0253-6269 [Print] Korea (South) |
PMID | 18087816
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
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Topics |
- Animals
- Cell Line, Tumor
- Cytokines
(pharmacology)
- Female
- Humans
- Immunotherapy, Adoptive
- Killer Cells, Natural
(immunology)
- Mice
- Ovarian Neoplasms
(pathology, therapy)
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