γδ T Cell Immunotherapy—A Review
Cancer immunotherapy utilizing Vγ9Vδ2 T cells has been developed over the past decade. A large number of clinical trials have been conducted on various types of solid tumors as well as hematological malignancies. Vγ9Vδ2 T cell-based immunotherapy can be classified into two categories based on the me...
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doaj-70b628880eb4422488713a36d6358a992020-11-25T01:46:32ZengMDPI AGPharmaceuticals1424-82472015-02-0181406110.3390/ph8010040ph8010040γδ T Cell Immunotherapy—A ReviewHirohito Kobayashi0Yoshimasa Tanaka1Transfusion Medicine and Cell Processing, Department of Urology, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanCenter for Therapeutic Innovation, Graduate School of Biomedical Sciences, Nagasaki University, 1-14 Bunkyo-machi, Nagasaki 852-8521, JapanCancer immunotherapy utilizing Vγ9Vδ2 T cells has been developed over the past decade. A large number of clinical trials have been conducted on various types of solid tumors as well as hematological malignancies. Vγ9Vδ2 T cell-based immunotherapy can be classified into two categories based on the methods of activation and expansion of these cells. Although the in vivo expansion of Vγ9Vδ2 T cells by phosphoantigens or nitrogen-containing bisphosphonates (N-bis) has been translated to early-phase clinical trials, in which the safety of the treatment was confirmed, problems such as activation-induced Vγ9Vδ2 T cell anergy and a decrease in the number of peripheral blood Vγ9Vδ2 T cells after infusion of these stimulants have not yet been solved. In addition, it is difficult to ex vivo expand Vγ9Vδ2 T cells from advanced cancer patients with decreased initial numbers of peripheral blood Vγ9Vδ2 T cells. In this article, we review the clinical studies and reports targeting Vγ9Vδ2 T cells and discuss the development and improvement of Vγ9Vδ2 T cell-based cancer immunotherapy.http://www.mdpi.com/1424-8247/8/1/40cancer immunotherapynitrogen-containing bisphosphonatephosphoantigentumorVγ9Vδ2 T cell |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hirohito Kobayashi Yoshimasa Tanaka |
spellingShingle |
Hirohito Kobayashi Yoshimasa Tanaka γδ T Cell Immunotherapy—A Review Pharmaceuticals cancer immunotherapy nitrogen-containing bisphosphonate phosphoantigen tumor Vγ9Vδ2 T cell |
author_facet |
Hirohito Kobayashi Yoshimasa Tanaka |
author_sort |
Hirohito Kobayashi |
title |
γδ T Cell Immunotherapy—A Review |
title_short |
γδ T Cell Immunotherapy—A Review |
title_full |
γδ T Cell Immunotherapy—A Review |
title_fullStr |
γδ T Cell Immunotherapy—A Review |
title_full_unstemmed |
γδ T Cell Immunotherapy—A Review |
title_sort |
γδ t cell immunotherapy—a review |
publisher |
MDPI AG |
series |
Pharmaceuticals |
issn |
1424-8247 |
publishDate |
2015-02-01 |
description |
Cancer immunotherapy utilizing Vγ9Vδ2 T cells has been developed over the past decade. A large number of clinical trials have been conducted on various types of solid tumors as well as hematological malignancies. Vγ9Vδ2 T cell-based immunotherapy can be classified into two categories based on the methods of activation and expansion of these cells. Although the in vivo expansion of Vγ9Vδ2 T cells by phosphoantigens or nitrogen-containing bisphosphonates (N-bis) has been translated to early-phase clinical trials, in which the safety of the treatment was confirmed, problems such as activation-induced Vγ9Vδ2 T cell anergy and a decrease in the number of peripheral blood Vγ9Vδ2 T cells after infusion of these stimulants have not yet been solved. In addition, it is difficult to ex vivo expand Vγ9Vδ2 T cells from advanced cancer patients with decreased initial numbers of peripheral blood Vγ9Vδ2 T cells. In this article, we review the clinical studies and reports targeting Vγ9Vδ2 T cells and discuss the development and improvement of Vγ9Vδ2 T cell-based cancer immunotherapy. |
topic |
cancer immunotherapy nitrogen-containing bisphosphonate phosphoantigen tumor Vγ9Vδ2 T cell |
url |
http://www.mdpi.com/1424-8247/8/1/40 |
work_keys_str_mv |
AT hirohitokobayashi gdtcellimmunotherapyareview AT yoshimasatanaka gdtcellimmunotherapyareview |
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1725018858878664704 |