Chimeric antigen receptors: unleashing a new age of anti-cancer therapy

Abstract Background Chimeric antigen receptors (CARs) represent a novel facet of modern day synthetic biology that exemplifies personalized medicine at work through their ability to harness and redirect a patient’s immune system to fight cancer. Body By combining the target-specificity of antibodies...

Full description

Bibliographic Details
Main Author: Yan Leyfman
Format: Article
Language:English
Published: BMC 2018-11-01
Series:Cancer Cell International
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12935-018-0685-x
id doaj-1842eee51b8e4364a0614dfb38a0674f
record_format Article
spelling doaj-1842eee51b8e4364a0614dfb38a0674f2020-11-25T02:17:19ZengBMCCancer Cell International1475-28672018-11-011811610.1186/s12935-018-0685-xChimeric antigen receptors: unleashing a new age of anti-cancer therapyYan Leyfman0Penn State College of MedicineAbstract Background Chimeric antigen receptors (CARs) represent a novel facet of modern day synthetic biology that exemplifies personalized medicine at work through their ability to harness and redirect a patient’s immune system to fight cancer. Body By combining the target-specificity of antibodies to the effector capabilities of T cells, CARs have yielded high remission rates for many late staged and relapsed/refractory (r/r) hematological malignancies, including acute lymphoblastic leukemias (ALL) and Non-Hodgkin’s lymphomas. Despite toxicities of cytokine release syndrome and neurotoxicity, recent studies have uncovered their underlying mechanisms and devised effective therapies to manage and possibly prevent them. In 2017, CAR T cell therapy became a reality for the general public despite the high costs, when Novartis’s Kymriah, became the first product to receive FDA approval for pediatric r/r B cell ALL with Gilead’s Yescarta following several months later. Although effective in hematological malignancies, CAR response has been limited in solid tumors largely attributed to the heterogeneous and immunosuppressive tumor microenvironment along tumor defense mechanisms, such as antigenic escape. Conclusion Despite the current challenges of CAR T therapy, this technology is still in its infancy and its promise will continue to grow as scientists continue to develop novel approaches to enhance its efficacy. As its prevalence continues to increase, institutions and pharmaceuticals worldwide are investing in this technology in hopes of driving therapeutic innovation, while providing greater access to their respective populations through clinical trials.http://link.springer.com/article/10.1186/s12935-018-0685-xChimeric antigen receptorLeukemiaHematological malignancyT cellImmunotherapySolid tumor
collection DOAJ
language English
format Article
sources DOAJ
author Yan Leyfman
spellingShingle Yan Leyfman
Chimeric antigen receptors: unleashing a new age of anti-cancer therapy
Cancer Cell International
Chimeric antigen receptor
Leukemia
Hematological malignancy
T cell
Immunotherapy
Solid tumor
author_facet Yan Leyfman
author_sort Yan Leyfman
title Chimeric antigen receptors: unleashing a new age of anti-cancer therapy
title_short Chimeric antigen receptors: unleashing a new age of anti-cancer therapy
title_full Chimeric antigen receptors: unleashing a new age of anti-cancer therapy
title_fullStr Chimeric antigen receptors: unleashing a new age of anti-cancer therapy
title_full_unstemmed Chimeric antigen receptors: unleashing a new age of anti-cancer therapy
title_sort chimeric antigen receptors: unleashing a new age of anti-cancer therapy
publisher BMC
series Cancer Cell International
issn 1475-2867
publishDate 2018-11-01
description Abstract Background Chimeric antigen receptors (CARs) represent a novel facet of modern day synthetic biology that exemplifies personalized medicine at work through their ability to harness and redirect a patient’s immune system to fight cancer. Body By combining the target-specificity of antibodies to the effector capabilities of T cells, CARs have yielded high remission rates for many late staged and relapsed/refractory (r/r) hematological malignancies, including acute lymphoblastic leukemias (ALL) and Non-Hodgkin’s lymphomas. Despite toxicities of cytokine release syndrome and neurotoxicity, recent studies have uncovered their underlying mechanisms and devised effective therapies to manage and possibly prevent them. In 2017, CAR T cell therapy became a reality for the general public despite the high costs, when Novartis’s Kymriah, became the first product to receive FDA approval for pediatric r/r B cell ALL with Gilead’s Yescarta following several months later. Although effective in hematological malignancies, CAR response has been limited in solid tumors largely attributed to the heterogeneous and immunosuppressive tumor microenvironment along tumor defense mechanisms, such as antigenic escape. Conclusion Despite the current challenges of CAR T therapy, this technology is still in its infancy and its promise will continue to grow as scientists continue to develop novel approaches to enhance its efficacy. As its prevalence continues to increase, institutions and pharmaceuticals worldwide are investing in this technology in hopes of driving therapeutic innovation, while providing greater access to their respective populations through clinical trials.
topic Chimeric antigen receptor
Leukemia
Hematological malignancy
T cell
Immunotherapy
Solid tumor
url http://link.springer.com/article/10.1186/s12935-018-0685-x
work_keys_str_mv AT yanleyfman chimericantigenreceptorsunleashinganewageofanticancertherapy
_version_ 1724887067730640896