机构:Texas Tech University Health Sciences Center,Department of Microbiology and Immunology
D. B. Lowe
M. H. Shearer
论文数: 0引用数: 0
h-index: 0
机构:Texas Tech University Health Sciences Center,Department of Microbiology and Immunology
M. H. Shearer
C. A. Jumper
论文数: 0引用数: 0
h-index: 0
机构:Texas Tech University Health Sciences Center,Department of Microbiology and Immunology
C. A. Jumper
R. C. Kennedy
论文数: 0引用数: 0
h-index: 0
机构:Texas Tech University Health Sciences Center,Department of Microbiology and Immunology
R. C. Kennedy
机构:
[1] Texas Tech University Health Sciences Center,Department of Microbiology and Immunology
[2] Texas Tech University Health Sciences Center,Internal Medicine
[3] Southwest Cancer Treatment and Research Center,undefined
来源:
Cellular and Molecular Life Sciences
|
2007年
/
64卷
关键词:
DNA vaccines;
cancer;
immunotherapy;
non-human primates;
animal models;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Cancer immunotherapy faces many obstacles that include eliciting immune reactions to self antigens as well as overcoming tumor-derived immunosuppressive networks and evasion tactics. Within the vaccine arsenal for inhibiting cancer proliferation, plasmid DNA represents a novel immunization strategy that is capable of eliciting both humoral and cellular arms of the immune response in addition to being safely administered and easily engineered and manufactured. Unfortunately, while DNA vaccines have performed well in preventing and treating malignancies in animal models, their overall application in human clinical trials has not impacted cancer regression to date. Since the establishment of these early trials, progress has been made in terms of increasing DNA vaccine immunogenicity and subverting the suppressive properties of tumor cells. Therefore, the success of future plasmid DNA use in cancer patients will depend on combinatorial strategies that enhance and direct the DNA vaccine immune response while also targeting tumor evasion mechanisms.