| Literature DB >> 24714356 |
Beom K Choi1, Sang C Lee, Myoung J Lee, Young H Kim, Young-Woo Kim, Keun-Won Ryu, Jun-Ho Lee, Su M Shin, Sang-Ho Lee, Susumu Suzuki, Ho S Oh, Chang H Kim, Don G Lee, Sun H Hwang, Eun-Mi Yu, In O Lee, Byoung S Kwon.
Abstract
Adoptive T-cell therapy is a promising approach to the immunotherapy of cancer, but for it to be a general cancer therapy a simple and standardized procedure for producing tumor-specific CD8 T cells is needed. On the basis of a unique property of 4-1BB (CD137), the selective expression on activated T cells, we have developed a simple and practical protocol to produce antigen-specific CD8 T cells from peripheral blood mononuclear cells. We have proved the feasibility of this procedure by isolating and expanding cytomegalovirus-specific CD8 T cells, and applied the procedure to produce Epstein-Barr virus (EBV)-specific CD8 T cells. By using this procedure, we could readily produce 10-10 antigen-specific CD8 T cells from 30 to 50 mL of blood in about 4 weeks. Moreover, our protocol allowed us to produce, from solid cancer patients, CD8 T cells that were specific for self/tumor antigens such as human telomerase reverse transcriptase (hTERT). It is interesting to note that, we were unable to amplify hTERT-specific CD8 T cells from healthy donors. Our protocol can be readily translated into cGMP-compliant production and is currently being used to produce EBV-specific CD8 T cells for phase I clinical trial. We believe that our method will provide a practical and effective option for adoptive T-cell therapy in the clinic.Entities:
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Year: 2014 PMID: 24714356 DOI: 10.1097/CJI.0000000000000027
Source DB: PubMed Journal: J Immunother ISSN: 1524-9557 Impact factor: 4.456