TY - JOUR
T1 - CARs
T2 - Synthetic Immunoreceptors for Cancer Therapy and Beyond
AU - Chang, Ze Nan L.
AU - Chen, Yvonne Y.
N1 - Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/5
Y1 - 2017/5
N2 - Chimeric antigen receptors (CARs) are versatile synthetic receptors that provide T cells with engineered specificity. Clinical success in treating B-cell malignancies has demonstrated the therapeutic potential of CAR-T cells against cancer, and efforts are underway to expand the use of engineered T cells to the treatment of diverse medical conditions, including infections and autoimmune diseases. Here, we review current understanding of the molecular properties of CARs, how this knowledge informs the rational design and characterization of novel receptors, the successes and shortcomings of CAR-T cells in the clinic, and emerging solutions for the continued improvement of CAR-T cell therapy.
AB - Chimeric antigen receptors (CARs) are versatile synthetic receptors that provide T cells with engineered specificity. Clinical success in treating B-cell malignancies has demonstrated the therapeutic potential of CAR-T cells against cancer, and efforts are underway to expand the use of engineered T cells to the treatment of diverse medical conditions, including infections and autoimmune diseases. Here, we review current understanding of the molecular properties of CARs, how this knowledge informs the rational design and characterization of novel receptors, the successes and shortcomings of CAR-T cells in the clinic, and emerging solutions for the continued improvement of CAR-T cell therapy.
KW - adoptive T-cell therapy
KW - chimeric antigen receptor (CAR)
KW - immunotherapy
KW - protein engineering
KW - synthetic biology
UR - http://www.scopus.com/inward/record.url?scp=85017449014&partnerID=8YFLogxK
U2 - 10.1016/j.molmed.2017.03.002
DO - 10.1016/j.molmed.2017.03.002
M3 - Review article
C2 - 28416139
AN - SCOPUS:85017449014
SN - 1471-4914
VL - 23
SP - 430
EP - 450
JO - Trends in Molecular Medicine
JF - Trends in Molecular Medicine
IS - 5
ER -