Abstract
Recent reports on the impressive efficacy of adoptively transferred T cells to challenge cancer in early phase clinical trials have significantly raised the profile of T cell therapy. Concomitantly, general expectations are also raised by these reports, with the natural aspiration to deliver this therapy over a wide range of tumor indications. Chimeric antigen receptors (CARs) endow T cell populations with defined antigen specificities that function independently of the natural T cell receptor and permit targeting of T cells towards virtually any tumor. Here, we review the current clinical application of CAR-T cells and relate clinical efficacy and safety of CAR-T cell trials to parameters considered critical for CAR engineering, classified as the three T's of CAR-T cell manipulation. © 2012 Elsevier Ltd.
Original language | English |
---|---|
Pages (from-to) | 377-384 |
Number of pages | 7 |
Journal | Trends in molecular medicine |
Volume | 18 |
Issue number | 7 |
DOIs | |
Publication status | Published - Jul 2012 |
Keywords
- Adoptive cell therapy
- Cancer
- Chimeric antigen receptor
- Gene transfer
- Immunotherapy
- T cell