Abstract
T-body or chimeric antigen receptor (CAR) technology, which combines the specificity of an antibody with the homing, tissue penetration, and target cell destruction of T cells, was first described in 1993. After many years of unmet promise, significant improvements in gene transfer, including the development of efficient retroviral vectors for transduction of human T cells, and better understanding of immunological pathways and immune cell interactions, are allowing this technology to reach a critical phase of evaluation, in which we will learn whether the approach can truly meet expectations. In this review we summarize the concept of CAR-based immunotherapy, describe the steps accomplished, and outline the future progress we need to make if this approach is truly to improve cancer immunotherapy.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1229-1239 |
| Number of pages | 11 |
| Journal | Human Gene Therapy |
| Volume | 20 |
| Issue number | 11 |
| DOIs | |
| State | Published - Nov 1 2009 |
ASJC Scopus subject areas
- Molecular Medicine
- Molecular Biology
- Genetics
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