Those of us working in clinical and medical technology and automation are most enthusiastic about our work when the instruments and techniques we are developing will directly affect patient well-being. The recent arrival of FDA-approved chimeric antigen receptor (CAR) T-cell therapies1,2 and the further expansion of T-cell and other cell-based therapies beyond oncology applications have reinvigorated discussions around the ways in which we harvest, culture, process, or directly alter therapeutic cells.
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Puleo et al. (2018) studied this question.
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