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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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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1724487126648619008 |