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Advances in research on immune escape mechanism of glioma

BACKGROUND: Glioma is the most common primary intracranial malignancy in clinical practice, and in particular, IDH‐wildtype glioblastoma has the worst prognosis. In recent years, surgical resection combined with simultaneous radiotherapy and immune checkpoint inhibitors has made some progress, but t...

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Detalles Bibliográficos
Autores principales: Guo, Xu, Wang, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324367/
https://www.ncbi.nlm.nih.gov/pubmed/37088950
http://dx.doi.org/10.1111/cns.14217
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author Guo, Xu
Wang, Gang
author_facet Guo, Xu
Wang, Gang
author_sort Guo, Xu
collection PubMed
description BACKGROUND: Glioma is the most common primary intracranial malignancy in clinical practice, and in particular, IDH‐wildtype glioblastoma has the worst prognosis. In recent years, surgical resection combined with simultaneous radiotherapy and immune checkpoint inhibitors has made some progress, but the efficacy is still not satisfactory, which may be related to the low immunogenicity of glioma cells and the tumor immunosuppressive microenvironment. METHODS: A comprehensive review of relevant literature was conducted to explore the mechanisms by which tumors suppress antitumor immune responses and produce escape, with a focus on the immune cells in the tumor microenvironment (TME). RESULTS: The mechanisms involved in immune evasion of glioma cells are complex and involve with immune cell differentiation and function. CONCLUSION: Our review emphasizes the need for a more profound comprehension of the mechanisms involved in immune response and immune evasion in glioma, to formulate more efficacious treatment modalities.
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spelling pubmed-103243672023-07-07 Advances in research on immune escape mechanism of glioma Guo, Xu Wang, Gang CNS Neurosci Ther Reviews BACKGROUND: Glioma is the most common primary intracranial malignancy in clinical practice, and in particular, IDH‐wildtype glioblastoma has the worst prognosis. In recent years, surgical resection combined with simultaneous radiotherapy and immune checkpoint inhibitors has made some progress, but the efficacy is still not satisfactory, which may be related to the low immunogenicity of glioma cells and the tumor immunosuppressive microenvironment. METHODS: A comprehensive review of relevant literature was conducted to explore the mechanisms by which tumors suppress antitumor immune responses and produce escape, with a focus on the immune cells in the tumor microenvironment (TME). RESULTS: The mechanisms involved in immune evasion of glioma cells are complex and involve with immune cell differentiation and function. CONCLUSION: Our review emphasizes the need for a more profound comprehension of the mechanisms involved in immune response and immune evasion in glioma, to formulate more efficacious treatment modalities. John Wiley and Sons Inc. 2023-04-23 /pmc/articles/PMC10324367/ /pubmed/37088950 http://dx.doi.org/10.1111/cns.14217 Text en © 2023 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Guo, Xu
Wang, Gang
Advances in research on immune escape mechanism of glioma
title Advances in research on immune escape mechanism of glioma
title_full Advances in research on immune escape mechanism of glioma
title_fullStr Advances in research on immune escape mechanism of glioma
title_full_unstemmed Advances in research on immune escape mechanism of glioma
title_short Advances in research on immune escape mechanism of glioma
title_sort advances in research on immune escape mechanism of glioma
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324367/
https://www.ncbi.nlm.nih.gov/pubmed/37088950
http://dx.doi.org/10.1111/cns.14217
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