| Autor: |
Maggard, Melinda, Meng, Lingzhong, Ke, Bibo, Allen, Rene, Devgan, Lara, Imagawa, David |
| Zdroj: |
Annals of Surgical Oncology: An Oncology Journal for Surgeons; Jan2001, Vol. 8 Issue 1, p32-37, 6p |
| Abstrakt: |
Background: The overexpression of transforming growth factor-beta (TGF-β) in hepatocellular carcinoma (HCC) appears to induce immunosuppression toward the tumor cells. Methods: A rat HCC cell line, Morris hepatoma rat cell line (MRH)-7777 (MRH), was transfected with antisense TGF-β2 in pCEP-4 vector and used as immunotherapy against the development of wild-type tumors. An enzyme-linked immunosorbent assay (ELISA) confirmed that TGF-β2 production was markedly lower for antisense modified cells as compared to wild-type tumor cells. Tumors were initiated by injecting MRH cells into the flanks of Buffalo rats. This was followed by biweekly vaccinations with irradiated MRH cells (unmodified, pCEP-4 alone, or antisense TGF-β2 modified). Results: In the group that received irradiated MRH unmodified cells, 55% of rats died from tumor burden, and 36% developed tumor regression. In the group that received irradiated MRH cells modified with pCEP-4 vector alone, 50% died from tumors and 33% had spontaneous regression. In animals treated with pCEP-4/TGF-β antisense modified cells, none developed tumors. Cell-mediated cytotoxicity assays demonstrated a twofold increase in lytic activity in the effector cells of the animals treated with antisense modified cells. Conclusions: These results demonstrate the successful treatment of HCC tumors in rats by a HCC vaccine genetically altered with antisense TGF-β2. Decreased production of TGF-β in HCC vaccine enhances immunogenicity against wild-type HCC tumor cells. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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