Fifteen years of gene therapy based on chimeric antigen receptors: "are we nearly there yet?"
- PMID: 19702437
- PMCID: PMC2829458
- DOI: 10.1089/hum.2009.142
Fifteen years of gene therapy based on chimeric antigen receptors: "are we nearly there yet?"
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.
Figures
References
-
- Ahmed N. Ratnayake M. Savoldo B. Perlaky L. Dotti G. Wels W.S. Bhattacharjee M.B. Gilbertson R.J. Shine H.D. Weiss H.L. Rooney C.M. Heslop H.E. Gottschalk S. Regression of experimental medulloblastoma following transfer of HER2-specific T cells. Cancer Res. 2007;67:5957–5964. - PubMed
-
- Andorsky D.J. Timmerman J.M. Interleukin-21: Biology and application to cancer therapy. Expert Opin. Biol. Ther. 2008;8:1295–1307. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical