Antitumor efficacy of tumor-antigen-encoding recombinant poxvirus immunization in Dunning rat prostate cancer: implications for clinical genetic vaccine development

被引:9
作者
Charles, LG
Xie, YC
Restifo, NP
Roessler, B
Sanda, MG
机构
[1] Univ Michigan, Sch Med, Dept Urol Surg, Taubman Ctr 2916, Ann Arbor, MI 48109 USA
[2] NCI, Surg Branch, Bethesda, MD 20892 USA
[3] Univ Michigan, Sch Med, Dept Med Rheumatol, Ann Arbor, MI USA
[4] Ann Arbor Vet Adm Med Ctr, Ann Arbor, MI USA
关键词
D O I
10.1007/s003450050186
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
One potential use for prostate-cancer-associated genes discovered through ongoing genetics studies entails the construction of virus- or plasmid-based recombinant vector vaccines encoding these new tumor-associated antigens (TAA) to induce TAA-specific immune responses for the prevention or therapy of prostate cancer. Clinical trials evaluating prototypes of such recombinant vaccines are under way. TAA-encoding recombinant vector vaccines, however, have not previously been evaluated in a prostate-cancer animal model. For assessment of the potential susceptibility of prostate cancer to genetic immunization strategies using TAA-encoding recombinant vectors. the antitumor efficacy of a model recombinant viral vector encoding a TAA was evaluated in rat Dunning prostate cancer. Recombinant vaccinia was chosen as a prototype virus vector encoding a TAA for these studies, and B-galactosidase was chosen as a model target TAA.
引用
收藏
页码:136 / 142
页数:7
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