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Targeting regulatory T cells in cytokine-induced killer cell cultures (Review)
Regulatory T cells (Tregs) are potent immunosuppressive cells that promote tumor growth and invasion by inducing immune escape and suppressing the antitumor immune response. Cytokine-induced killer (CIK) cells are considered to be the primary candidate for adoptive immunotherapy due to their strong...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990197/ https://www.ncbi.nlm.nih.gov/pubmed/24748966 http://dx.doi.org/10.3892/br.2014.234 |
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author | TAO, QIANSHAN WANG, HUIPING ZHAI, ZHIMIN |
author_facet | TAO, QIANSHAN WANG, HUIPING ZHAI, ZHIMIN |
author_sort | TAO, QIANSHAN |
collection | PubMed |
description | Regulatory T cells (Tregs) are potent immunosuppressive cells that promote tumor growth and invasion by inducing immune escape and suppressing the antitumor immune response. Cytokine-induced killer (CIK) cells are considered to be the primary candidate for adoptive immunotherapy due to their strong antitumor activity. It was recently reported that the concomitant presence of Tregs may decrease the cytotoxicity of CIK cells. Therefore, depletion or downregulation of Tregs in CIK cell cultures by optimizing the culture program may enhance CIK cell cytotoxicity in vitro and in vivo. The aim of the present review was to summarize the currently available studies on the optimal culture strategy for improving the antitumor activity of CIK cells through targeting Tregs. |
format | Online Article Text |
id | pubmed-3990197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-39901972014-04-18 Targeting regulatory T cells in cytokine-induced killer cell cultures (Review) TAO, QIANSHAN WANG, HUIPING ZHAI, ZHIMIN Biomed Rep Articles Regulatory T cells (Tregs) are potent immunosuppressive cells that promote tumor growth and invasion by inducing immune escape and suppressing the antitumor immune response. Cytokine-induced killer (CIK) cells are considered to be the primary candidate for adoptive immunotherapy due to their strong antitumor activity. It was recently reported that the concomitant presence of Tregs may decrease the cytotoxicity of CIK cells. Therefore, depletion or downregulation of Tregs in CIK cell cultures by optimizing the culture program may enhance CIK cell cytotoxicity in vitro and in vivo. The aim of the present review was to summarize the currently available studies on the optimal culture strategy for improving the antitumor activity of CIK cells through targeting Tregs. D.A. Spandidos 2014-05 2014-02-07 /pmc/articles/PMC3990197/ /pubmed/24748966 http://dx.doi.org/10.3892/br.2014.234 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles TAO, QIANSHAN WANG, HUIPING ZHAI, ZHIMIN Targeting regulatory T cells in cytokine-induced killer cell cultures (Review) |
title | Targeting regulatory T cells in cytokine-induced killer cell cultures (Review) |
title_full | Targeting regulatory T cells in cytokine-induced killer cell cultures (Review) |
title_fullStr | Targeting regulatory T cells in cytokine-induced killer cell cultures (Review) |
title_full_unstemmed | Targeting regulatory T cells in cytokine-induced killer cell cultures (Review) |
title_short | Targeting regulatory T cells in cytokine-induced killer cell cultures (Review) |
title_sort | targeting regulatory t cells in cytokine-induced killer cell cultures (review) |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3990197/ https://www.ncbi.nlm.nih.gov/pubmed/24748966 http://dx.doi.org/10.3892/br.2014.234 |
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