Engineering cell-based therapies to interface robustly with host physiology

被引:16
作者
Schwarz, Kelly A. [1 ]
Leonard, Joshua N. [1 ,2 ,3 ]
机构
[1] Northwestern Univ, Dept Chem & Biol Engn, 2145 Sheridan Rd, Evanston, IL 60208 USA
[2] Northwestern Univ, Chem Life Proc Inst, 2170 Campus Dr, Evanston, IL 60208 USA
[3] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, 675 N St Clair, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
Mammalian synthetic biology; Biosensors; Cell-based therapies; Gene circuits; RED-BLOOD-CELLS; T-CELLS; SLEEPING-BEAUTY; ADENOASSOCIATED VIRUS; SYNTHETIC BIOLOGY; GENE-THERAPY; TRANSGENE EXPRESSION; CANCER-IMMUNOTHERAPY; TARGETED INTEGRATION; ADOPTIVE TRANSFER;
D O I
10.1016/j.addr.2016.05.019
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 65
页数:11
相关论文
共 129 条
  • [91] Escherichia coli-Cloned CFTR Loci Relevant for Human Artificial Chromosome Therapy
    Rocchi, Lucia
    Braz, Carla
    Cattani, Sonja
    Ramalho, Anabela
    Christan, Sulith
    Edlinger, Marlene
    Ascenzioni, Fiorentina
    Laner, Andreas
    Kraner, Simone
    Amaral, Margarida
    Schindelhauer, Dirk
    [J]. HUMAN GENE THERAPY, 2010, 21 (09) : 1077 - 1092
  • [92] Bile acid-controlled transgene expression in mammalian cells and mice
    Roessger, Katrin
    Charpin-El-Hamri, Ghislaine
    Fussenegger, Martin
    [J]. METABOLIC ENGINEERING, 2014, 21 : 81 - 90
  • [93] A closed-loop synthetic gene circuit for the treatment of diet-induced obesity in mice
    Roessger, Katrin
    Charpin-El-Hamri, Ghislaine
    Fussenegger, Martin
    [J]. NATURE COMMUNICATIONS, 2013, 4
  • [94] Precision Tumor Recognition by T Cells With Combinatorial Antigen-Sensing Circuits
    Roybal, Kole T.
    Rupp, Levi J.
    Morsut, Leonardo
    Walker, Whitney J.
    McNally, Krista A.
    Park, Jason S.
    Lim, Wendell A.
    [J]. CELL, 2016, 164 (04) : 770 - 779
  • [95] AAV-Mediated Gene Therapy for Research and Therapeutic Purposes
    Samulski, R. Jude
    Muzyczka, Nicholas
    [J]. ANNUAL REVIEW OF VIROLOGY, VOL 1, 2014, 1 : 427 - 451
  • [96] TARGETED INTEGRATION OF ADENOASSOCIATED VIRUS (AAV) INTO HUMAN CHROMOSOME-19
    SAMULSKI, RJ
    ZHU, X
    XIAO, X
    BROOK, JD
    HOUSMAN, DE
    EPSTEIN, N
    HUNTER, LA
    [J]. EMBO JOURNAL, 1991, 10 (12) : 3941 - 3950
  • [97] Directed evolution of a G protein-coupled receptor for expression, stability, and binding selectivity
    Sarkar, Casim A.
    Dodevski, Igor
    Kenig, Manca
    Dudli, Stefan
    Mohr, Anja
    Hermans, Emmanuel
    Plueckthun, Andreas
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (39) : 14808 - 14813
  • [98] CD28 costimulation improves expansion and persistence of chimeric antigen receptor-modified T cells in lymphoma patients
    Savoldo, Barbara
    Ramos, Carlos Almeida
    Liu, Enli
    Mims, Martha P.
    Keating, Michael J.
    Carrum, George
    Kamble, Rammurti T.
    Bollard, Catherine M.
    Gee, Adrian P.
    Mei, Zhuyong
    Liu, Hao
    Grilley, Bambi
    Rooney, Cliona M.
    Heslop, Helen E.
    Brenner, Malcolm K.
    Dotti, Gianpietro
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (05) : 1822 - 1826
  • [99] Post-translational enzyme activation in an animal via optimized conditional protein splicing
    Schwartz, Edmund C.
    Saez, Lino
    Young, Michael W.
    Muir, Tom W.
    [J]. NATURE CHEMICAL BIOLOGY, 2007, 3 (01) : 50 - 54
  • [100] Genetically engineered T cells bearing chimeric nanoconstructed receptors harboring TAG-72-specific camelid single domain antibodies as targeting agents
    Sharifzadeh, Zahra
    Rahbarizadeh, Fatemeh
    Shokrgozar, Mohammad A.
    Ahmadvand, Davoud
    Mahboudi, Fereidoun
    Jamnani, Fatemeh Rahimi
    Moghimi, S. Moein
    [J]. CANCER LETTERS, 2013, 334 (02) : 237 - 244