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CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells
CD161 is a C-type lectin-like receptor expressed on the majority of natural killer (NK) cells; however, the significance of CD161 expression on NK cells has not been comprehensively investigated. Recently, we found that CD161 expression identifies a transcriptional and innate functional phenotype th...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900032/ https://www.ncbi.nlm.nih.gov/pubmed/29686665 http://dx.doi.org/10.3389/fimmu.2018.00486 |
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author | Kurioka, Ayako Cosgrove, Cormac Simoni, Yannick van Wilgenburg, Bonnie Geremia, Alessandra Björkander, Sophia Sverremark-Ekström, Eva Thurnheer, Christine Günthard, Huldrych F. Khanna, Nina Walker, Lucy Jane Arancibia-Cárcamo, Carolina V. Newell, Evan W. Willberg, Christian B. Klenerman, Paul |
author_facet | Kurioka, Ayako Cosgrove, Cormac Simoni, Yannick van Wilgenburg, Bonnie Geremia, Alessandra Björkander, Sophia Sverremark-Ekström, Eva Thurnheer, Christine Günthard, Huldrych F. Khanna, Nina Walker, Lucy Jane Arancibia-Cárcamo, Carolina V. Newell, Evan W. Willberg, Christian B. Klenerman, Paul |
author_sort | Kurioka, Ayako |
collection | PubMed |
description | CD161 is a C-type lectin-like receptor expressed on the majority of natural killer (NK) cells; however, the significance of CD161 expression on NK cells has not been comprehensively investigated. Recently, we found that CD161 expression identifies a transcriptional and innate functional phenotype that is shared across various T cell populations. Using mass cytometry and microarray experiments, we demonstrate that this functional phenotype extends to NK cells. CD161 marks NK cells that have retained the ability to respond to innate cytokines during their differentiation, and is lost upon cytomegalovirus-induced maturation in both healthy and human immunodeficiency virus (HIV)-infected patients. These pro-inflammatory NK cells are present in the inflamed lamina propria where they are enriched for integrin CD103 expression. Thus, CD161 expression identifies NK cells that may contribute to inflammatory disease pathogenesis and correlates with an innate responsiveness to cytokines in both T and NK cells. |
format | Online Article Text |
id | pubmed-5900032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59000322018-04-23 CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells Kurioka, Ayako Cosgrove, Cormac Simoni, Yannick van Wilgenburg, Bonnie Geremia, Alessandra Björkander, Sophia Sverremark-Ekström, Eva Thurnheer, Christine Günthard, Huldrych F. Khanna, Nina Walker, Lucy Jane Arancibia-Cárcamo, Carolina V. Newell, Evan W. Willberg, Christian B. Klenerman, Paul Front Immunol Immunology CD161 is a C-type lectin-like receptor expressed on the majority of natural killer (NK) cells; however, the significance of CD161 expression on NK cells has not been comprehensively investigated. Recently, we found that CD161 expression identifies a transcriptional and innate functional phenotype that is shared across various T cell populations. Using mass cytometry and microarray experiments, we demonstrate that this functional phenotype extends to NK cells. CD161 marks NK cells that have retained the ability to respond to innate cytokines during their differentiation, and is lost upon cytomegalovirus-induced maturation in both healthy and human immunodeficiency virus (HIV)-infected patients. These pro-inflammatory NK cells are present in the inflamed lamina propria where they are enriched for integrin CD103 expression. Thus, CD161 expression identifies NK cells that may contribute to inflammatory disease pathogenesis and correlates with an innate responsiveness to cytokines in both T and NK cells. Frontiers Media S.A. 2018-04-09 /pmc/articles/PMC5900032/ /pubmed/29686665 http://dx.doi.org/10.3389/fimmu.2018.00486 Text en Copyright © 2018 Kurioka, Cosgrove, Simoni, van Wilgenburg, Geremia, Björkander, Sverremark-Ekström, Thurnheer, Günthard, Khanna, The Swiss HIV Cohort Study, Oxford IBD Cohort Investigators, Walker, Arancibia-Cárcamo, Newell, Willberg and Klenerman. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Kurioka, Ayako Cosgrove, Cormac Simoni, Yannick van Wilgenburg, Bonnie Geremia, Alessandra Björkander, Sophia Sverremark-Ekström, Eva Thurnheer, Christine Günthard, Huldrych F. Khanna, Nina Walker, Lucy Jane Arancibia-Cárcamo, Carolina V. Newell, Evan W. Willberg, Christian B. Klenerman, Paul CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells |
title | CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells |
title_full | CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells |
title_fullStr | CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells |
title_full_unstemmed | CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells |
title_short | CD161 Defines a Functionally Distinct Subset of Pro-Inflammatory Natural Killer Cells |
title_sort | cd161 defines a functionally distinct subset of pro-inflammatory natural killer cells |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5900032/ https://www.ncbi.nlm.nih.gov/pubmed/29686665 http://dx.doi.org/10.3389/fimmu.2018.00486 |
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