TY - JOUR
T1 - Engineering cell-based therapies to interface robustly with host physiology
AU - Schwarz, Kelly A.
AU - Leonard, Joshua N.
N1 - Funding Information:
KAS was supported in part by the National Institutes of Health T32 Training Grant GM 008449 through Northwestern University's Biotechnology Training Program and by the Defense Advanced Research Projects Agency, Award number W911NF-11-2-0066 (to JNL). No funding sources had any involvement in the writing of this manuscript. The human silhouette image (Fig. 2), was generated by Freepix and is used here under a creative common license.
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/10/1
Y1 - 2016/10/1
N2 - Engineered cell-based therapies comprise a rapidly growing clinical technology for treating disease by leveraging the natural capabilities of cells, including migration, information transduction, and biosynthesis and secretion. There now exists a substantial portfolio of intracellular and extracellular sensors that enable bioengineers to program cells to execute defined responses to specific changes in state or environmental cues. As our capability to construct more sophisticated cellular programs increases, assessing and improving the degree to which cell-based therapies perform as desired in vivo will become an increasingly important consideration and opportunity for technological advancement. In this review, we seek to describe both current capabilities and potential needs for building cell-based therapies that interface with host physiology in a manner that is robust — a phrase we use in this context to describe the achievement of therapeutic efficacy across a range of patients and implementations. We first review the portfolio of sensors and outputs currently available for use in cell-based therapies by highlighting key advancements and current gaps. Then, we propose a conceptual framework for evaluating and pursuing robust clinical performance of engineered cell-based therapies.
AB - Engineered cell-based therapies comprise a rapidly growing clinical technology for treating disease by leveraging the natural capabilities of cells, including migration, information transduction, and biosynthesis and secretion. There now exists a substantial portfolio of intracellular and extracellular sensors that enable bioengineers to program cells to execute defined responses to specific changes in state or environmental cues. As our capability to construct more sophisticated cellular programs increases, assessing and improving the degree to which cell-based therapies perform as desired in vivo will become an increasingly important consideration and opportunity for technological advancement. In this review, we seek to describe both current capabilities and potential needs for building cell-based therapies that interface with host physiology in a manner that is robust — a phrase we use in this context to describe the achievement of therapeutic efficacy across a range of patients and implementations. We first review the portfolio of sensors and outputs currently available for use in cell-based therapies by highlighting key advancements and current gaps. Then, we propose a conceptual framework for evaluating and pursuing robust clinical performance of engineered cell-based therapies.
KW - Biosensors
KW - Cell-based therapies
KW - Gene circuits
KW - Mammalian synthetic biology
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U2 - 10.1016/j.addr.2016.05.019
DO - 10.1016/j.addr.2016.05.019
M3 - Review article
C2 - 27266446
AN - SCOPUS:84991056000
SN - 0169-409X
VL - 105
SP - 55
EP - 65
JO - Advanced Drug Delivery Reviews
JF - Advanced Drug Delivery Reviews
ER -