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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Main Authors: Hirohito Kobayashi, Yoshimasa Tanaka
Format: Article
Language:English
Published: MDPI AG 2015-02-01
Series:Pharmaceuticals
Subjects:
Online Access:http://www.mdpi.com/1424-8247/8/1/40
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spelling 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
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