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Regulation of MHC I Molecules in Glioblastoma Cells and the Sensitizing of NK Cells
Immunotherapy has been established as an important area in the therapy of malignant diseases. Immunogenicity sufficient for immune recognition and subsequent elimination can be bypassed by tumors through altered and/or reduced expression levels of major histocompatibility complex class I (MHC I) mol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998501/ https://www.ncbi.nlm.nih.gov/pubmed/33800301 http://dx.doi.org/10.3390/ph14030236 |
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author | Burster, Timo Gärtner, Fabian Bulach, Christiane Zhanapiya, Anuar Gihring, Adrian Knippschild, Uwe |
author_facet | Burster, Timo Gärtner, Fabian Bulach, Christiane Zhanapiya, Anuar Gihring, Adrian Knippschild, Uwe |
author_sort | Burster, Timo |
collection | PubMed |
description | Immunotherapy has been established as an important area in the therapy of malignant diseases. Immunogenicity sufficient for immune recognition and subsequent elimination can be bypassed by tumors through altered and/or reduced expression levels of major histocompatibility complex class I (MHC I) molecules. Natural killer (NK) cells can eliminate tumor cells in a MHC I antigen presentation-independent manner by an array of activating and inhibitory receptors, which are promising candidates for immunotherapy. Here we summarize the latest findings in recognizing and regulating MHC I molecules that affect NK cell surveillance of glioblastoma cells. |
format | Online Article Text |
id | pubmed-7998501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79985012021-03-28 Regulation of MHC I Molecules in Glioblastoma Cells and the Sensitizing of NK Cells Burster, Timo Gärtner, Fabian Bulach, Christiane Zhanapiya, Anuar Gihring, Adrian Knippschild, Uwe Pharmaceuticals (Basel) Review Immunotherapy has been established as an important area in the therapy of malignant diseases. Immunogenicity sufficient for immune recognition and subsequent elimination can be bypassed by tumors through altered and/or reduced expression levels of major histocompatibility complex class I (MHC I) molecules. Natural killer (NK) cells can eliminate tumor cells in a MHC I antigen presentation-independent manner by an array of activating and inhibitory receptors, which are promising candidates for immunotherapy. Here we summarize the latest findings in recognizing and regulating MHC I molecules that affect NK cell surveillance of glioblastoma cells. MDPI 2021-03-08 /pmc/articles/PMC7998501/ /pubmed/33800301 http://dx.doi.org/10.3390/ph14030236 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Review Burster, Timo Gärtner, Fabian Bulach, Christiane Zhanapiya, Anuar Gihring, Adrian Knippschild, Uwe Regulation of MHC I Molecules in Glioblastoma Cells and the Sensitizing of NK Cells |
title | Regulation of MHC I Molecules in Glioblastoma Cells and the Sensitizing of NK Cells |
title_full | Regulation of MHC I Molecules in Glioblastoma Cells and the Sensitizing of NK Cells |
title_fullStr | Regulation of MHC I Molecules in Glioblastoma Cells and the Sensitizing of NK Cells |
title_full_unstemmed | Regulation of MHC I Molecules in Glioblastoma Cells and the Sensitizing of NK Cells |
title_short | Regulation of MHC I Molecules in Glioblastoma Cells and the Sensitizing of NK Cells |
title_sort | regulation of mhc i molecules in glioblastoma cells and the sensitizing of nk cells |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998501/ https://www.ncbi.nlm.nih.gov/pubmed/33800301 http://dx.doi.org/10.3390/ph14030236 |
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