Producer T cells: Using genetically engineered T cells as vehicles to generate and deliver therapeutics to tumors

被引:15
|
作者
Tsai, Alexander K. [1 ]
Davila, Eduardo [1 ,2 ]
机构
[1] Univ Maryland, Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD 21201 USA
[2] Univ Maryland, Dept Microbiol & Immunol, Baltimore, MD 21201 USA
来源
ONCOIMMUNOLOGY | 2016年 / 5卷 / 05期
关键词
Adoptive transfer; cell vehicle; cancer therapy; drug delivery; genetic engineering; T cell; STEM-CELLS; IN-VIVO; ANTITUMOR-ACTIVITY; EXOGENOUS IL-2; CLINICAL-TRIAL; LONG-TERM; CANCER; LYMPHOCYTES; INTERLEUKIN-12; EXPRESSION;
D O I
10.1080/2162402X.2015.1122158
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adoptive cell transfer (ACT) is an emerging anticancer therapy that has shown promise in various malignancies. Redirecting antigen specificity by genetically engineering T cells to stably express receptors has become an effective variant of ACT. A novel extension of this approach is to utilize engineered T cells to produce and deliver anticancer therapeutics that enhance cytotoxic T cell function and simultaneously inhibit immunosuppressive processes. Here, we review the potential of using T cells as therapeutic-secreting vehicles for immunotherapies and present theoretical and established arguments in support of further development of this unique cell-based immunotherapy.
引用
收藏
页数:9
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