4.6 Review

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

期刊

ONCOIMMUNOLOGY
卷 5, 期 5, 页码 -

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/2162402X.2015.1122158

关键词

Adoptive transfer; cell vehicle; cancer therapy; drug delivery; genetic engineering; T cell

资金

  1. NIH National Cancer Institute (NCI) [R01CA140917, R01CA166961]
  2. Melanoma Research Foundation
  3. University of Maryland, Baltimore
  4. Marlene and Stewart Greenebaum Cancer Center
  5. [T32CA154274]

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据