细胞毒性T细胞
CTL公司*
病毒学
遗传增强
抗体
生物
转染
病毒复制
病毒载体
腺病毒感染
腺病毒科
癌症研究
癌细胞
癌症
细胞培养
病毒
免疫学
基因
体外
生物化学
遗传学
重组DNA
作者
Katsuyuki Hamada,Junzo Desaki,Kou Nakagawa,Ting Zhang,Toshiro Shirakawa,Akinobu Gotoh,Masatoshi Tagawa
标识
DOI:10.1038/sj.mt.6300128
摘要
Although replication-competent viruses have been developed to treat cancers, their cytotoxic effects are insufficient, as infection is inhibited by the generation of neutralizing antibodies. To address this limitation, we developed a carrier cell system to deliver a replication-competent adenovirus. Carrier cells infected with replication-competent adenovirus were incubated with target cancer cells in a high titer of anti-adenovirus antibody. Carrier cells were injected into syngeneic subcutaneous tumors after immunization with adenovirus. Carrier cell-derived cell fragments containing viral particles were engulfed by proliferative target cancer cells. This engulfment-mediated transfer of adenovirus was not inhibited by the anti-adenovirus antibody and enabled repetitive infection. After the induction of anti-adenoviral cytotoxic T-lymphocyte (CTL) responses by immunization with adenovirus, administration of carrier cells infected with a replication-competent adenovirus induced complete tumor regression. Adenovirus-GM-CSF augmented the anti-tumor effect of carrier cells by increasing anti-adenoviral and anti-tumoral CTL responses and decreased the number of injections of carrier cells required to induce complete tumor regression. This novel carrier cell-mediated viral transfection system might prove useful in a variety of cancer therapies.
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