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We previously reported that systemic injection of recombinant adenovirus resulted in a rim of gene transduction around experimental liver tumor nodules. This zone of higher infection is dependent on the alpha(v)beta(3) integrin, acting as an adenovirus internalization receptor, which is overexpressed in tissues surrounding liver metastases. When a recombinant adenovirus encoding interleukin-12 (AdCMVIL-12) is given into a subcutaneous tumor nodule in mice also bearing concomitant liver tumors, a fraction of AdCMVIL-12 reaches the systemic circulation and infects liver tissue, especially at the malignant/healthy tissue interface. As a result of the expression at this location of the interleukin-12 transgenes, VCAM-1 is induced on vessel cells and mediates the recruitment of adoptively transferred anti-tumor cytolytic T-lymphocytes. These studies provide mechanistic explanations for the potent therapeutic synergy observed between interleukin-12 gene transfer and adoptive T-cell therapy.

Original publication

DOI

10.1006/mthe.2001.0317

Type

Journal article

Journal

Molecular therapy : the journal of the American Society of Gene Therapy

Publication Date

05/2001

Volume

3

Pages

665 - 672

Addresses

Gene Therapy Unit, University of Navarra School of Medicine, C/Irunlarrea, I 31008 Pamplona, Spain.

Keywords

Endothelium, Lymphocytes, T-Lymphocytes, T-Lymphocytes, Cytotoxic, Animals, Mice, Inbred BALB C, Mice, Adenoviridae, Colonic Neoplasms, Liver Neoplasms, Neoplasm Metastasis, Indoles, Galactosides, Vascular Cell Adhesion Molecule-1, Receptors, Vitronectin, Interleukin-12, Antibodies, Monoclonal, Microscopy, Fluorescence, Flow Cytometry, Cell Separation, Immunohistochemistry, Cell Adhesion, Cell Movement, Transgenes, Female