Genetically modified T cells for the treatment of malignant disease

Transfus Med Hemother. 2013 Dec;40(6):388-402. doi: 10.1159/000357163. Epub 2013 Nov 29.

Abstract

The broaden application of adoptive T-cell transfer has been constrained by the technical abilities to isolate and expand antigen-specific T cells potent to selectively kill tumor cells. With the recent progress in the design and manufacturing of cellular products, T cells used in the treatment of malignant diseases may be regarded as anticancer biopharmaceuticals. Genetical manipulation of T cells has given T cells desired specificity but also enable to tailor their activation and proliferation potential. Here, we summarize the recent developments in genetic engineering of T-cell-based biopharmaceuticals, covering criteria for their clinical application in regard to safety and efficacy.

Keywords: Adoptive cell transfer; CAR; Chimeric antigen receptor; Clinical trial; T-cell receptor; TCR.

Publication types

  • Review