Increasing the safety and efficacy of chimeric antigen receptor T cell therapy
Abstract Chimeric antigen receptor (CAR) T cell therapy is a promising cancer treatment that has recently been undergoing rapid development. However, there are still some major challenges, including precise tumor targeting to avoid off-target or “on-target/off-tumor” toxicity, adequate T cell infilt...
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doaj-c34dcc870a4e4a96b0fd628c138238ed2020-11-24T20:59:04ZengSpringerOpenProtein & Cell1674-800X1674-80182017-04-018857358910.1007/s13238-017-0411-9Increasing the safety and efficacy of chimeric antigen receptor T cell therapyHua Li0Yangbing Zhao1Center for Cellular Immunotherapies, Perelman School of Medicine, University of PennsylvaniaCenter for Cellular Immunotherapies, Perelman School of Medicine, University of PennsylvaniaAbstract Chimeric antigen receptor (CAR) T cell therapy is a promising cancer treatment that has recently been undergoing rapid development. However, there are still some major challenges, including precise tumor targeting to avoid off-target or “on-target/off-tumor” toxicity, adequate T cell infiltration and migration to solid tumors and T cell proliferation and persistence across the physical and biochemical barriers of solid tumors. In this review, we focus on the primary challenges and strategies to design safe and effective CAR T cells, including using novel cutting-edge technologies for CAR and vector designs to increase both the safety and efficacy, further T cell modification to overcome the tumor-associated immune suppression, and using gene editing technologies to generate universal CAR T cells. All these efforts promote the development and evolution of CAR T cell therapy and move toward our ultimate goal—curing cancer with high safety, high efficacy, and low cost.http://link.springer.com/article/10.1007/s13238-017-0411-9chimeric antigen receptorscancer adoptive immunotherapyT lymphocytesgene therapygene editing |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hua Li Yangbing Zhao |
spellingShingle |
Hua Li Yangbing Zhao Increasing the safety and efficacy of chimeric antigen receptor T cell therapy Protein & Cell chimeric antigen receptors cancer adoptive immunotherapy T lymphocytes gene therapy gene editing |
author_facet |
Hua Li Yangbing Zhao |
author_sort |
Hua Li |
title |
Increasing the safety and efficacy of chimeric antigen receptor T cell therapy |
title_short |
Increasing the safety and efficacy of chimeric antigen receptor T cell therapy |
title_full |
Increasing the safety and efficacy of chimeric antigen receptor T cell therapy |
title_fullStr |
Increasing the safety and efficacy of chimeric antigen receptor T cell therapy |
title_full_unstemmed |
Increasing the safety and efficacy of chimeric antigen receptor T cell therapy |
title_sort |
increasing the safety and efficacy of chimeric antigen receptor t cell therapy |
publisher |
SpringerOpen |
series |
Protein & Cell |
issn |
1674-800X 1674-8018 |
publishDate |
2017-04-01 |
description |
Abstract Chimeric antigen receptor (CAR) T cell therapy is a promising cancer treatment that has recently been undergoing rapid development. However, there are still some major challenges, including precise tumor targeting to avoid off-target or “on-target/off-tumor” toxicity, adequate T cell infiltration and migration to solid tumors and T cell proliferation and persistence across the physical and biochemical barriers of solid tumors. In this review, we focus on the primary challenges and strategies to design safe and effective CAR T cells, including using novel cutting-edge technologies for CAR and vector designs to increase both the safety and efficacy, further T cell modification to overcome the tumor-associated immune suppression, and using gene editing technologies to generate universal CAR T cells. All these efforts promote the development and evolution of CAR T cell therapy and move toward our ultimate goal—curing cancer with high safety, high efficacy, and low cost. |
topic |
chimeric antigen receptors cancer adoptive immunotherapy T lymphocytes gene therapy gene editing |
url |
http://link.springer.com/article/10.1007/s13238-017-0411-9 |
work_keys_str_mv |
AT huali increasingthesafetyandefficacyofchimericantigenreceptortcelltherapy AT yangbingzhao increasingthesafetyandefficacyofchimericantigenreceptortcelltherapy |
_version_ |
1716783938338291712 |