Production method for iPS cell-derived genetically diverse T cell colony
A technology of genetic diversity and cell population, applied in the field of regenerative T cell population, can solve the problems of T cell fatigue, decreased antigen immune response, etc., and achieve the effect of high therapeutic effect
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[0053] Methods for producing iPS cells are well known in the art. In one aspect of the present invention, iPS cells are preferably prepared by introducing reprogramming factors into the T cell population concentrated in step (1). Here, examples of reprogramming factors include Oct3 / 4, Sox2, Sox1, Sox3, Sox15, Sox17, Klf4, Klf2, c-Myc, N-Myc, L-Myc, Nanog, Lin28, Fbx15, ERas, ECAT15 -2, Tcl1, beta-catenin, Lin28b, Sall1, Sall4, Esrrb, Nr5a2, Tbx3 or Glis1 and other genes or gene products, the reprogramming factors can be used alone or in combination.
[0054] ・Procedure for culturing established iPS cells while maintaining genetic diversity
[0055] Passaging is preferably performed in culturing iPS cells. However, in a general passaging method, cells other than those used for passaging are discarded, so that the diversity of an iPS cell population established from a genetically diverse T cell population is gradually lost.
[0056] In this regard, in one aspect of the pres...
Embodiment 1
[0134] Using the method described above, iPS cells were established from genetically diverse T cell populations isolated from excised tumors of lung cancer patients, and induced to redifferentiate into genetically diverse T cells.
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