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Fates of CD8+ T cells in Tumor Microenvironment

Studies have reported a positive correlation between elevated CD8+ T cells in the tumor microenvironment (TME) and good prognosis in cancer. However, the mechanisms linking T cell tumor-infiltration and tumor rejection are yet to be fully understood. The cells and factors of the TME facilitate tumor...

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Autores principales: Maimela, Nomathamsanqa Resegofetse, Liu, Shasha, Zhang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297055/
https://www.ncbi.nlm.nih.gov/pubmed/30581539
http://dx.doi.org/10.1016/j.csbj.2018.11.004
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author Maimela, Nomathamsanqa Resegofetse
Liu, Shasha
Zhang, Yi
author_facet Maimela, Nomathamsanqa Resegofetse
Liu, Shasha
Zhang, Yi
author_sort Maimela, Nomathamsanqa Resegofetse
collection PubMed
description Studies have reported a positive correlation between elevated CD8+ T cells in the tumor microenvironment (TME) and good prognosis in cancer. However, the mechanisms linking T cell tumor-infiltration and tumor rejection are yet to be fully understood. The cells and factors of the TME facilitate tumor development in various ways. CD8+ T cell function is influenced by a number of factors, including CD8+ T cell trafficking and localization into tumor sites; as well as CD8+ T cell growth and differentiation. This review highlights recent literature as well as currently evolving concepts regarding the fates of CD8+ T cells in the TME from three different aspects CD8+ T cell trafficking, differentiation and function. A thorough understanding of factors contributing to the fates of CD8+ T cells will allow researchers to develop new strategies and improve on already existing strategies to facilitate CD8+ T cell mediated anti-tumor function, impede T cell dysfunction and modulate the TME into a less immunosuppressive TME.
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spelling pubmed-62970552018-12-21 Fates of CD8+ T cells in Tumor Microenvironment Maimela, Nomathamsanqa Resegofetse Liu, Shasha Zhang, Yi Comput Struct Biotechnol J Review Article Studies have reported a positive correlation between elevated CD8+ T cells in the tumor microenvironment (TME) and good prognosis in cancer. However, the mechanisms linking T cell tumor-infiltration and tumor rejection are yet to be fully understood. The cells and factors of the TME facilitate tumor development in various ways. CD8+ T cell function is influenced by a number of factors, including CD8+ T cell trafficking and localization into tumor sites; as well as CD8+ T cell growth and differentiation. This review highlights recent literature as well as currently evolving concepts regarding the fates of CD8+ T cells in the TME from three different aspects CD8+ T cell trafficking, differentiation and function. A thorough understanding of factors contributing to the fates of CD8+ T cells will allow researchers to develop new strategies and improve on already existing strategies to facilitate CD8+ T cell mediated anti-tumor function, impede T cell dysfunction and modulate the TME into a less immunosuppressive TME. Research Network of Computational and Structural Biotechnology 2018-11-22 /pmc/articles/PMC6297055/ /pubmed/30581539 http://dx.doi.org/10.1016/j.csbj.2018.11.004 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review Article
Maimela, Nomathamsanqa Resegofetse
Liu, Shasha
Zhang, Yi
Fates of CD8+ T cells in Tumor Microenvironment
title Fates of CD8+ T cells in Tumor Microenvironment
title_full Fates of CD8+ T cells in Tumor Microenvironment
title_fullStr Fates of CD8+ T cells in Tumor Microenvironment
title_full_unstemmed Fates of CD8+ T cells in Tumor Microenvironment
title_short Fates of CD8+ T cells in Tumor Microenvironment
title_sort fates of cd8+ t cells in tumor microenvironment
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6297055/
https://www.ncbi.nlm.nih.gov/pubmed/30581539
http://dx.doi.org/10.1016/j.csbj.2018.11.004
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