Vaccination of fusion cells of rat dendritic and carcinoma cells prevents tumor growth in vivo
✍ Scribed by Masaya Kawada; Hitoshi Ikeda; Toshiyuki Takahashi; Akihiro Ishizu; Hiroshi Ishikura; Hiroyuki Katoh; Takashi Yoshiki
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 400 KB
- Volume
- 105
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Several reports on immunotherapy using dendritic cells‐based vaccine have been published. We investigated findings using fusion cells (FCs) generated from rat dendritic cells and a syngeneic hepatic cancer cell line with regard to inducing anti‐tumor immunity. Vaccination of rats using FCs protected against growth of the subcutaneously implanted tumor in vivo and induced infiltration of CD8^+^ T cells into the tumor. At the site of CD8^+^ T cell infiltration, there were apoptotic tumor cells. T cells from spleen of FCs‐vaccinated rats with protective ability against tumor growth included tumor specific cytotoxic CD8^+^ T cells restricted to major histocompatibility complex Class I. In addition, adaptive transfer of in vitro re‐stimulated splenic T cells with FCs was effective in preventing tumor growth and in vivo vaccinations of rats with FCs after resection of the subcutaneous implanted tumor inhibited local tumor recurrences. Immunotherapy using FCs appears to be an effective method if used in combination with surgical or other anti‐cancer therapies. © 2003 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
## Abstract Dendritic cells (DCs) are antigen presenting cells that play a role in T‐cell activation. Liver‐associated natural killer T lymphocytes (NKTs) are a unique subset of lymphocytes that may be important in antitumor immunity. Hepatitis B virus (HBV)‐associated hepatocellular carcinoma (HCC
## Abstract ## Background Although cancer therapy using replication‐selective oncolytic adenoviruses has been available for many years, its anti‐tumor efficacy is suboptimal as a result of low and nonspecific infectivity that depends on coxsackie adenovirus receptor expression of the target cancer