Abstract
Background Tumor-associated antigens (TAAs) are known to be immunotherapy targets; thus tumor-sharing TAA may be used as a fusion hybrid partner to confer protection against subsequent tumor challenge. Methods The squamous cell carcinomas (SCCs), SCCVII and B4B8, were used in C3H/HEN mice: SCCVII (H-2 k) is syngeneic, B4B8 (H-2d) is allogeneic. Experiments using tumor alone included hyperimmunization schedule, subdermal and intranodal routes. Mice were challenged 2 weeks later. Fusion hybrids were created from both SCC tumor cell lines and syngeneic dendritic cells (DCs). These were delivered intranodally for immunization, and mice were challenged with tumor 2 weeks later. Results Only syngeneic tumor given subdermally was able to protect after tumor challenge 2 weeks later. Hyperimmunization schedule did not alter these findings. However, fusion hybrid immunization from both allogeneic and syngeneic SCCs conferred protection after tumor challenge. Conclusions Allogeneic tumor-DC fusion hybrids targeting TAA can protect against subsequent tumor challenge.
Original language | English (US) |
---|---|
Pages (from-to) | 1209-1216 |
Number of pages | 8 |
Journal | Head and Neck |
Volume | 32 |
Issue number | 9 |
DOIs | |
State | Published - Sep 1 2010 |
Keywords
- dendritic cell
- fusion hybrid
- immunotherapy
- squamous cell carcinoma
- vaccine
ASJC Scopus subject areas
- Otorhinolaryngology