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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:
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.
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页数:9
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