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10.1016/j.stem.2015.03.011

http://scihub22266oqcxt.onion/10.1016/j.stem.2015.03.011
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C5611846!5611846!25842976
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suck abstract from ncbi


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pmid25842976      Cell+Stem+Cell 2015 ; 16 (4): 357-66
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  • New Cell Sources for T Cell Engineering and Adoptive Immunotherapy #MMPMID25842976
  • Themeli M; Rivière I; Sadelain M
  • Cell Stem Cell 2015[Apr]; 16 (4): 357-66 PMID25842976show ga
  • The promising clinical results obtained with engineered T cells, including chimeric antigen receptor (CAR) therapy, call for further advancements to facilitate and broaden their applicability. One potentially beneficial innovation is to exploit new T cell sources that reduce the need for autologous cell manufacturing and enable cell transfer across histocompatibility barriers. Here we review emerging T cell engineering approaches that utilize alternative T cell sources, which include virus-specific or T cell receptor-less allogeneic T cells, expanded lymphoid progenitors, and induced pluripotent stem cell (iPSC)-derived T lymphocytes. The latter offer the prospect for true off-the-shelf, genetically enhanced, histocompatible cell therapy products.
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