Podoplanin as an Attractive Target of CAR T Cell Therapy

To date, various kinds of cancer immunotherapy methods have been developed, but T cell immunotherapy is one of the most promising strategies. In general, T cell receptor (TCR) or chimeric antigen receptor (CAR) is used to modify the antigen specificity of T cells. CARs possess an underlying potentia...

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Main Authors: Masazumi Waseda, Shin Kaneko
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/9/9/1971
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spelling doaj-df2afc6afbe843e7a3299990f71421b12020-11-25T03:51:32ZengMDPI AGCells2073-44092020-08-0191971197110.3390/cells9091971Podoplanin as an Attractive Target of CAR T Cell TherapyMasazumi Waseda0Shin Kaneko1Shin Kaneko Laboratory, Department of Cell Growth and Differentiation, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto 606-8507, JapanShin Kaneko Laboratory, Department of Cell Growth and Differentiation, Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto 606-8507, JapanTo date, various kinds of cancer immunotherapy methods have been developed, but T cell immunotherapy is one of the most promising strategies. In general, T cell receptor (TCR) or chimeric antigen receptor (CAR) is used to modify the antigen specificity of T cells. CARs possess an underlying potential with treatment efficacy to treat a broad range of cancer patients compared with TCRs. Although a variety of CAR molecules have been developed so far, the clinical application for solid tumors is limited partly due to its adverse effect known as “on-target off-tumor toxicity”. Therefore, it is very important for CAR T cell therapy to target specific antigens exclusively expressed by malignant cells. Here, we review the application of T cell immunotherapy using specific antigen receptor molecules and discuss the possibility of the clinical application of podoplanin-targeted CAR derived from a cancer-specific monoclonal antibody (CasMab).https://www.mdpi.com/2073-4409/9/9/1971T cell immunotherapytumor-specific antigenchimeric antigen receptor (CAR)cancer-specific monoclonal antibody (CasMab)induced pluripotent stem (iPS) cell
collection DOAJ
language English
format Article
sources DOAJ
author Masazumi Waseda
Shin Kaneko
spellingShingle Masazumi Waseda
Shin Kaneko
Podoplanin as an Attractive Target of CAR T Cell Therapy
Cells
T cell immunotherapy
tumor-specific antigen
chimeric antigen receptor (CAR)
cancer-specific monoclonal antibody (CasMab)
induced pluripotent stem (iPS) cell
author_facet Masazumi Waseda
Shin Kaneko
author_sort Masazumi Waseda
title Podoplanin as an Attractive Target of CAR T Cell Therapy
title_short Podoplanin as an Attractive Target of CAR T Cell Therapy
title_full Podoplanin as an Attractive Target of CAR T Cell Therapy
title_fullStr Podoplanin as an Attractive Target of CAR T Cell Therapy
title_full_unstemmed Podoplanin as an Attractive Target of CAR T Cell Therapy
title_sort podoplanin as an attractive target of car t cell therapy
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2020-08-01
description To date, various kinds of cancer immunotherapy methods have been developed, but T cell immunotherapy is one of the most promising strategies. In general, T cell receptor (TCR) or chimeric antigen receptor (CAR) is used to modify the antigen specificity of T cells. CARs possess an underlying potential with treatment efficacy to treat a broad range of cancer patients compared with TCRs. Although a variety of CAR molecules have been developed so far, the clinical application for solid tumors is limited partly due to its adverse effect known as “on-target off-tumor toxicity”. Therefore, it is very important for CAR T cell therapy to target specific antigens exclusively expressed by malignant cells. Here, we review the application of T cell immunotherapy using specific antigen receptor molecules and discuss the possibility of the clinical application of podoplanin-targeted CAR derived from a cancer-specific monoclonal antibody (CasMab).
topic T cell immunotherapy
tumor-specific antigen
chimeric antigen receptor (CAR)
cancer-specific monoclonal antibody (CasMab)
induced pluripotent stem (iPS) cell
url https://www.mdpi.com/2073-4409/9/9/1971
work_keys_str_mv AT masazumiwaseda podoplaninasanattractivetargetofcartcelltherapy
AT shinkaneko podoplaninasanattractivetargetofcartcelltherapy
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