Strategies for cancer gene therapy using adenoviral vectors

被引：8

作者：

Descamps, V ^{[1
]}

Duffour, MT ^{[1
]}

Mathieu, MC ^{[1
]}

Fernandez, N ^{[1
]}

Cordier, L ^{[1
]}

Abina, MA ^{[1
]}

Kremer, E ^{[1
]}

Perricaudet, M ^{[1
]}

Haddada, H ^{[1
]}

机构：

[1] INST GUSTAVE ROUSSY,F-94805 VILLEJUIF,FRANCE

来源：

JOURNAL OF MOLECULAR MEDICINE-JMM | 1996年 / 74卷 / 04期

关键词：

adenoviral vector; gene therapy; cancer; immunotherapy;

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Modification of tumor cells using gene transfer either to enhance host immunity or to act directly on tumor cells is being intensively studied in animal models. Remarkable results have yielded to approved clinical protocols in the treatment of cancer patients using this approach. Several methods of gene delivery have been developed. This article is particularly devoted to the interest of the use of adenoviral vectors in the different strategies of cancer gene therapy.

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收藏

页码：183 / 189

页数：7

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