Driving CARs into Sweet Roads: Targeting Glycosylated Antigens in Cancer

Engineering T cells with chimeric antigen receptors (CARs) has demonstrated remarkable success in eradicating hematological malignancies. In this issue of Immunity, June and colleagues demonstrate the broad antitumor efficacy of a newly-designed CAR targeting the O-linked hypoglycosylated epitopes T...

Descripción completa

Detalles Bibliográficos
Autor principal: Mariño, Karina V.
Publicado: 2016
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10747613_v44_n6_p1248_Blidner
http://hdl.handle.net/20.500.12110/paper_10747613_v44_n6_p1248_Blidner
Aporte de:
id paper:paper_10747613_v44_n6_p1248_Blidner
record_format dspace
spelling paper:paper_10747613_v44_n6_p1248_Blidner2023-06-08T16:05:10Z Driving CARs into Sweet Roads: Targeting Glycosylated Antigens in Cancer Mariño, Karina V. antigen artificial receptor carbohydrate antigen carcinoembryonic antigen chimeric antigen receptor cytotoxic T lymphocyte antigen 4 epidermal growth factor receptor 2 epitope gamma interferon ganglioside GD2 glycosylated antigen glycosylated protein interleukin 2 lentivirus vector mesothelin monoclonal antibody mucin 1 programmed death 1 ligand 1 programmed death 1 receptor single chain fragment variable antibody theratope Tn antigen tumor marker unclassified drug acute lymphoblastic leukemia antineoplastic activity breast cancer cancer immunization cancer immunotherapy cell therapy clinical trial (topic) cytotoxicity drug targeting genetic engineering hematologic malignancy human lymphatic system tumor malignant transformation neoplasm nonhuman priority journal Short Survey solid tumor T cell leukemia T lymphocyte glycosylation immunology neoplasm Glycosylation Humans Neoplasms T-Lymphocytes Engineering T cells with chimeric antigen receptors (CARs) has demonstrated remarkable success in eradicating hematological malignancies. In this issue of Immunity, June and colleagues demonstrate the broad antitumor efficacy of a newly-designed CAR targeting the O-linked hypoglycosylated epitopes Tn and sialyl-Tn on cancer-associated MUC-1. Engineering T cells with chimeric antigen receptors (CARs) has demonstrated remarkable success in eradicating hematological malignancies. June and colleagues demonstrate the broad antitumor efficacy of a newly-designed CAR targeting the O-linked hypoglycosylated epitopes Tn and sialyl-Tn on cancer-associated MUC-1. © 2016 Elsevier Inc. Fil:Mariño, K.V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2016 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10747613_v44_n6_p1248_Blidner http://hdl.handle.net/20.500.12110/paper_10747613_v44_n6_p1248_Blidner
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic antigen
artificial receptor
carbohydrate antigen
carcinoembryonic antigen
chimeric antigen receptor
cytotoxic T lymphocyte antigen 4
epidermal growth factor receptor 2
epitope
gamma interferon
ganglioside GD2
glycosylated antigen
glycosylated protein
interleukin 2
lentivirus vector
mesothelin
monoclonal antibody
mucin 1
programmed death 1 ligand 1
programmed death 1 receptor
single chain fragment variable antibody
theratope
Tn antigen
tumor marker
unclassified drug
acute lymphoblastic leukemia
antineoplastic activity
breast cancer
cancer immunization
cancer immunotherapy
cell therapy
clinical trial (topic)
cytotoxicity
drug targeting
genetic engineering
hematologic malignancy
human
lymphatic system tumor
malignant transformation
neoplasm
nonhuman
priority journal
Short Survey
solid tumor
T cell leukemia
T lymphocyte
glycosylation
immunology
neoplasm
Glycosylation
Humans
Neoplasms
T-Lymphocytes
spellingShingle antigen
artificial receptor
carbohydrate antigen
carcinoembryonic antigen
chimeric antigen receptor
cytotoxic T lymphocyte antigen 4
epidermal growth factor receptor 2
epitope
gamma interferon
ganglioside GD2
glycosylated antigen
glycosylated protein
interleukin 2
lentivirus vector
mesothelin
monoclonal antibody
mucin 1
programmed death 1 ligand 1
programmed death 1 receptor
single chain fragment variable antibody
theratope
Tn antigen
tumor marker
unclassified drug
acute lymphoblastic leukemia
antineoplastic activity
breast cancer
cancer immunization
cancer immunotherapy
cell therapy
clinical trial (topic)
cytotoxicity
drug targeting
genetic engineering
hematologic malignancy
human
lymphatic system tumor
malignant transformation
neoplasm
nonhuman
priority journal
Short Survey
solid tumor
T cell leukemia
T lymphocyte
glycosylation
immunology
neoplasm
Glycosylation
Humans
Neoplasms
T-Lymphocytes
Mariño, Karina V.
Driving CARs into Sweet Roads: Targeting Glycosylated Antigens in Cancer
topic_facet antigen
artificial receptor
carbohydrate antigen
carcinoembryonic antigen
chimeric antigen receptor
cytotoxic T lymphocyte antigen 4
epidermal growth factor receptor 2
epitope
gamma interferon
ganglioside GD2
glycosylated antigen
glycosylated protein
interleukin 2
lentivirus vector
mesothelin
monoclonal antibody
mucin 1
programmed death 1 ligand 1
programmed death 1 receptor
single chain fragment variable antibody
theratope
Tn antigen
tumor marker
unclassified drug
acute lymphoblastic leukemia
antineoplastic activity
breast cancer
cancer immunization
cancer immunotherapy
cell therapy
clinical trial (topic)
cytotoxicity
drug targeting
genetic engineering
hematologic malignancy
human
lymphatic system tumor
malignant transformation
neoplasm
nonhuman
priority journal
Short Survey
solid tumor
T cell leukemia
T lymphocyte
glycosylation
immunology
neoplasm
Glycosylation
Humans
Neoplasms
T-Lymphocytes
description Engineering T cells with chimeric antigen receptors (CARs) has demonstrated remarkable success in eradicating hematological malignancies. In this issue of Immunity, June and colleagues demonstrate the broad antitumor efficacy of a newly-designed CAR targeting the O-linked hypoglycosylated epitopes Tn and sialyl-Tn on cancer-associated MUC-1. Engineering T cells with chimeric antigen receptors (CARs) has demonstrated remarkable success in eradicating hematological malignancies. June and colleagues demonstrate the broad antitumor efficacy of a newly-designed CAR targeting the O-linked hypoglycosylated epitopes Tn and sialyl-Tn on cancer-associated MUC-1. © 2016 Elsevier Inc.
author Mariño, Karina V.
author_facet Mariño, Karina V.
author_sort Mariño, Karina V.
title Driving CARs into Sweet Roads: Targeting Glycosylated Antigens in Cancer
title_short Driving CARs into Sweet Roads: Targeting Glycosylated Antigens in Cancer
title_full Driving CARs into Sweet Roads: Targeting Glycosylated Antigens in Cancer
title_fullStr Driving CARs into Sweet Roads: Targeting Glycosylated Antigens in Cancer
title_full_unstemmed Driving CARs into Sweet Roads: Targeting Glycosylated Antigens in Cancer
title_sort driving cars into sweet roads: targeting glycosylated antigens in cancer
publishDate 2016
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_10747613_v44_n6_p1248_Blidner
http://hdl.handle.net/20.500.12110/paper_10747613_v44_n6_p1248_Blidner
work_keys_str_mv AT marinokarinav drivingcarsintosweetroadstargetingglycosylatedantigensincancer
_version_ 1768542562237284352