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Regeneration of tumor antigen-specific CTLs utilizing iPS technology

  • Takuya Maeda
  • , Kyoko Masuda
  • , Hiroshi Kawamoto

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

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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