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The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells
Human natural killer (NK) cells are cytotoxic effector cells that are increasingly harnessed in cancer immunotherapy. NKG2A/CD94 is an inhibitory receptor on NK cells that has established regulatory functions in the direct interaction with target cells when engaged with its ligand, the non-classical...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310841/ https://www.ncbi.nlm.nih.gov/pubmed/37386090 http://dx.doi.org/10.1038/s41598-023-37779-6 |
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author | Kaulfuss, Meike Mietz, Juliane Fabri, Astrid vom Berg, Johannes Münz, Christian Chijioke, Obinna |
author_facet | Kaulfuss, Meike Mietz, Juliane Fabri, Astrid vom Berg, Johannes Münz, Christian Chijioke, Obinna |
author_sort | Kaulfuss, Meike |
collection | PubMed |
description | Human natural killer (NK) cells are cytotoxic effector cells that are increasingly harnessed in cancer immunotherapy. NKG2A/CD94 is an inhibitory receptor on NK cells that has established regulatory functions in the direct interaction with target cells when engaged with its ligand, the non-classical HLA class I molecule HLA-E. Here, we confirmed NKG2A as a checkpoint molecule in primary human NK cells and identified a novel role for NKG2A in maintaining NK cell expansion capacity by dampening both proliferative activity and excessive activation-induced cell death. Maintenance of NK cell expansion capacity might contribute to the preferential accumulation of human NKG2A(+) NK cells after hematopoietic cell transplantation and enrichment of functionally impaired NK cells in human cancers. Functional silencing of NKG2A for cancer immunotherapy is highly attractive but will need to consider that this might also lead to a reduced survival by driving activation-induced cell death in targeted NK cells. |
format | Online Article Text |
id | pubmed-10310841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103108412023-07-01 The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells Kaulfuss, Meike Mietz, Juliane Fabri, Astrid vom Berg, Johannes Münz, Christian Chijioke, Obinna Sci Rep Article Human natural killer (NK) cells are cytotoxic effector cells that are increasingly harnessed in cancer immunotherapy. NKG2A/CD94 is an inhibitory receptor on NK cells that has established regulatory functions in the direct interaction with target cells when engaged with its ligand, the non-classical HLA class I molecule HLA-E. Here, we confirmed NKG2A as a checkpoint molecule in primary human NK cells and identified a novel role for NKG2A in maintaining NK cell expansion capacity by dampening both proliferative activity and excessive activation-induced cell death. Maintenance of NK cell expansion capacity might contribute to the preferential accumulation of human NKG2A(+) NK cells after hematopoietic cell transplantation and enrichment of functionally impaired NK cells in human cancers. Functional silencing of NKG2A for cancer immunotherapy is highly attractive but will need to consider that this might also lead to a reduced survival by driving activation-induced cell death in targeted NK cells. Nature Publishing Group UK 2023-06-29 /pmc/articles/PMC10310841/ /pubmed/37386090 http://dx.doi.org/10.1038/s41598-023-37779-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Kaulfuss, Meike Mietz, Juliane Fabri, Astrid vom Berg, Johannes Münz, Christian Chijioke, Obinna The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells |
title | The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells |
title_full | The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells |
title_fullStr | The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells |
title_full_unstemmed | The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells |
title_short | The NK cell checkpoint NKG2A maintains expansion capacity of human NK cells |
title_sort | nk cell checkpoint nkg2a maintains expansion capacity of human nk cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310841/ https://www.ncbi.nlm.nih.gov/pubmed/37386090 http://dx.doi.org/10.1038/s41598-023-37779-6 |
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