par Cheong, Siew Chiat
;Blangenois, Isabelle
;Franssen, Jean-Denis
;Servais, Charlotte
;Phan, Vy;Trakatelli, Myrto Georgia
;Bruyns, Catherine
;Vile, Richard;Velu, Thierry
;Brandenburger, Anne-Nicole 
Référence The journal of gene medicine, 8, 7, page (919-928)
Publication Publié, 2006-07
;Blangenois, Isabelle
;Franssen, Jean-Denis
;Servais, Charlotte
;Phan, Vy;Trakatelli, Myrto Georgia
;Bruyns, Catherine
;Vile, Richard;Velu, Thierry
;Brandenburger, Anne-Nicole 
Référence The journal of gene medicine, 8, 7, page (919-928)
Publication Publié, 2006-07
Article révisé par les pairs
| Résumé : | Hybrids obtained by fusion between tumour cells (TC) and dendritic cells (DC) have been proposed as anti-tumour vaccines because of their potential to combine the expression of tumour-associated antigens with efficient antigen presentation. The classical methods used for fusion, polyethylene glycol (PEG) and electrofusion, are cytotoxic and generate cell debris that can be taken up by DC rendering the identification of true hybrids difficult. |



