par Lespagnard, Laurence
;Mettens, Pascal
;Verheyden, Anouk;Tasiaux, Nicole
;Thielemans, Kris;Van Meirvenne, Sonja;Geldhof, A;De Baetselier, Patrick;Urbain, Jacques
;Leo, Oberdan
;Moser, Muriel 
Référence International journal of cancer, 76, 2, page (250-258)
Publication Publié, 1998-04






Référence International journal of cancer, 76, 2, page (250-258)
Publication Publié, 1998-04
Article révisé par les pairs
Résumé : | Characterization of the spontaneous immune response that frequently occurs in tumor-bearing animals, as well as immunization using dendritic cells pulsed with tumor antigens, suggests that a limiting factor of the tumor-specific immune response may be a defect in the co-stimulatory signal that is required for optimal activation of T cells. In this work, we describe a new approach to improve the antigen-presenting capacity of tumor cells, which does not require a source of purified tumor-associated antigen. We fused P815 mastocytoma cells with bone marrow-derived dendritic cells. We obtained one hybrid that displayed the phenotypic and functional properties of dendritic cells and expressed mRNA coding for the tumor-associated antigen P815 A/B. Injections of irradiated hybrid cells prevented the growth of preimplanted mastocytoma and induced long-lasting tumor resistance. |