| Literature DB >> 20336155 |
M Compte1, V Alonso-Camino, P Santos-Valle, A M Cuesta, D Sánchez-Martín, M R López, J L Vicario, C Salas, L Sanz, L Alvarez-Vallina.
Abstract
Several works have shown the feasibility of engineering functional blood vessels in vivo using human endothelial cells (ECs). Going further, we explored the therapeutic potential of neovessels after gene-modifying the ECs for the secretion of a therapeutic protein. Given that these vessels are connected with the host vascular bed, we hypothesized that systemic release of the expressed protein is immediate. As a proof of principle, we used primary human ECs transduced with a lentiviral vector for the expression of a recombinant bispecific alphaCEA/alphaCD3 antibody. These ECs, along with mesenchymal stem cells as a source of mural cells, were embedded in Matrigel and subcutaneously implanted in nude mice. High antibody levels were detected in plasma for 1 month. Furthermore, the antibody exerted a therapeutic effect in mice bearing distant carcinoembryonic-antigen (CEA)-positive tumors after inoculation of human T cells. In summary, we show for the first time the therapeutic effect of a protein locally secreted by engineered human neovessels.Entities:
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Year: 2010 PMID: 20336155 DOI: 10.1038/gt.2010.33
Source DB: PubMed Journal: Gene Ther ISSN: 0969-7128 Impact factor: 5.250