抄録
Tumor immunotherapy, especially tumor antigen specific T cell therapy, is currently attracting attention. However, a critical issue still awaits resolution; it is difficult to efficiently expand tumor antigen-specific T cells. To solve this problem, we are now utilizing iPS cell technology. When iPS cells are established from tumor antigen specific T cells, T cells regenerated from these iPS cells are expected to express the same TCRs as the original T cells. In line with this concept, we succeeded in regenerating tumor antigen specific cytotoxic T cells. The regenerated T cells exhibited TCR specific killing activity comparable to that of the original cells, and were able to kill leukemia cells in an antigen-specific manner. We are currently endeavoring to apply this method clinically. In the future, we intend to establish an allogeneic transfusion system, in which various tumor antigen specific T-iPS cells from a wide range of HLA haplotype homozygous donors will be lined up as a "T-iPS cell bank", with the aim of making off-the-shelf tumor immunotherapy a reality.
| 本文言語 | 英語 |
|---|---|
| ページ(範囲) | 1066-1073 |
| ページ数 | 8 |
| ジャーナル | [Rinsho ketsueki] The Japanese journal of clinical hematology |
| 巻 | 57 |
| 号 | 8 |
| DOI | |
| 出版ステータス | 出版済み - 01-08-2016 |
All Science Journal Classification (ASJC) codes
- 医学一般
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