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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381201/ https://www.ncbi.nlm.nih.gov/pubmed/25686210 http://dx.doi.org/10.3390/ph8010040 |
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author | Kobayashi, Hirohito Tanaka, Yoshimasa |
author_facet | Kobayashi, Hirohito Tanaka, Yoshimasa |
author_sort | Kobayashi, Hirohito |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-4381201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-43812012015-04-30 γδ T Cell Immunotherapy—A Review Kobayashi, Hirohito Tanaka, Yoshimasa Pharmaceuticals (Basel) 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 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. MDPI 2015-02-12 /pmc/articles/PMC4381201/ /pubmed/25686210 http://dx.doi.org/10.3390/ph8010040 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kobayashi, Hirohito Tanaka, Yoshimasa γδ T Cell Immunotherapy—A Review |
title | 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_short | γδ T Cell Immunotherapy—A Review |
title_sort | γδ t cell immunotherapy—a review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381201/ https://www.ncbi.nlm.nih.gov/pubmed/25686210 http://dx.doi.org/10.3390/ph8010040 |
work_keys_str_mv | AT kobayashihirohito gdtcellimmunotherapyareview AT tanakayoshimasa gdtcellimmunotherapyareview |