The major goal in cancer immunotherapy is the induction of tumor-specific T lymphocytes capable of killing tumor cells. As both dendritic cells (DCs) and interleukin-12 (IL-12) can play immunostimulatory roles in vivo, the use of a combination of these has become a promising approach. In the present
Dendritic cells fused with mastocytoma cells elicit therapeutic antitumor immunity
โ Scribed by Laurence Lespagnard; Pascal Mettens; Anne-Marie Verheyden; Nicole Tasiaux; Kris Thielemans; Sonja van Meirvenne; Anja Geldhof; Patrick De Baetselier; Jacques Urbain; Oberdan Leo; Muriel Moser
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- French
- Weight
- 183 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
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 antigenpresenting 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.
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