4.6 Review

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

Journal

ONCOIMMUNOLOGY
Volume 5, Issue 5, Pages -

Publisher

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

Keywords

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

Funding

  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]

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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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