Regeneration of tumor antigen-specific CTLs utilizing iPS technology

Takuya Maeda, Kyoko Masuda, Hiroshi Kawamoto

研究成果: Article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English
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
57
8
DOI
出版ステータスPublished - 01-08-2016
外部発表はい

All Science Journal Classification (ASJC) codes

  • 医学(全般)

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