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The peripheral differentiation of human natural killer T cells
The peripheral maturation of human CD1d‐restricted natural killer T (NKT) cells has not been well described. In this study, we identified four major subsets of NKT cells in adults, distinguished by the expression of CD4, CD8 and CCR5. Phenotypic analysis suggested a hierarchical pattern of different...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767057/ https://www.ncbi.nlm.nih.gov/pubmed/30875134 http://dx.doi.org/10.1111/imcb.12248 |
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author | Liu, Jie Hill, Brenna J Darko, Sam Song, Kaimei Quigley, Máire F Asher, Tedi E Morita, Yohei Greenaway, Hui Y Venturi, Vanessa Douek, Daniel C Davenport, Miles P Price, David A Roederer, Mario |
author_facet | Liu, Jie Hill, Brenna J Darko, Sam Song, Kaimei Quigley, Máire F Asher, Tedi E Morita, Yohei Greenaway, Hui Y Venturi, Vanessa Douek, Daniel C Davenport, Miles P Price, David A Roederer, Mario |
author_sort | Liu, Jie |
collection | PubMed |
description | The peripheral maturation of human CD1d‐restricted natural killer T (NKT) cells has not been well described. In this study, we identified four major subsets of NKT cells in adults, distinguished by the expression of CD4, CD8 and CCR5. Phenotypic analysis suggested a hierarchical pattern of differentiation, whereby immature CD4(+) CD8(−) CCR5(−) cells progressed to an intermediate CD4(+) CD8(−) CCR5(+) stage, which remained less differentiated than the CD4(−) CD8(−) and CD4(−) CD8(+) subsets, both of which expressed CCR5. This interpretation was supported by functional data, including clonogenic potential and cytokine secretion profiles, as well as T‐cell receptor (TCR) excision circle analysis. Moreover, conventional and high‐throughput sequencing of the corresponding TCR repertoires demonstrated significant clonotypic overlap within individuals, especially between the more differentiated CD4(−) CD8(−) and CD4(−) CD8(+) subsets. Collectively, these results mapped a linear differentiation pathway across the post‐thymic landscape of human CD1d‐restricted NKT cells. |
format | Online Article Text |
id | pubmed-6767057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67670572019-10-01 The peripheral differentiation of human natural killer T cells Liu, Jie Hill, Brenna J Darko, Sam Song, Kaimei Quigley, Máire F Asher, Tedi E Morita, Yohei Greenaway, Hui Y Venturi, Vanessa Douek, Daniel C Davenport, Miles P Price, David A Roederer, Mario Immunol Cell Biol Original Articles The peripheral maturation of human CD1d‐restricted natural killer T (NKT) cells has not been well described. In this study, we identified four major subsets of NKT cells in adults, distinguished by the expression of CD4, CD8 and CCR5. Phenotypic analysis suggested a hierarchical pattern of differentiation, whereby immature CD4(+) CD8(−) CCR5(−) cells progressed to an intermediate CD4(+) CD8(−) CCR5(+) stage, which remained less differentiated than the CD4(−) CD8(−) and CD4(−) CD8(+) subsets, both of which expressed CCR5. This interpretation was supported by functional data, including clonogenic potential and cytokine secretion profiles, as well as T‐cell receptor (TCR) excision circle analysis. Moreover, conventional and high‐throughput sequencing of the corresponding TCR repertoires demonstrated significant clonotypic overlap within individuals, especially between the more differentiated CD4(−) CD8(−) and CD4(−) CD8(+) subsets. Collectively, these results mapped a linear differentiation pathway across the post‐thymic landscape of human CD1d‐restricted NKT cells. John Wiley and Sons Inc. 2019-04-08 2019-07 /pmc/articles/PMC6767057/ /pubmed/30875134 http://dx.doi.org/10.1111/imcb.12248 Text en © 2019 The Authors. Immunology & Cell Biology published by John Wiley & Sons Australia, Ltd on behalf of Australasian Society for Immunology Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Liu, Jie Hill, Brenna J Darko, Sam Song, Kaimei Quigley, Máire F Asher, Tedi E Morita, Yohei Greenaway, Hui Y Venturi, Vanessa Douek, Daniel C Davenport, Miles P Price, David A Roederer, Mario The peripheral differentiation of human natural killer T cells |
title | The peripheral differentiation of human natural killer T cells |
title_full | The peripheral differentiation of human natural killer T cells |
title_fullStr | The peripheral differentiation of human natural killer T cells |
title_full_unstemmed | The peripheral differentiation of human natural killer T cells |
title_short | The peripheral differentiation of human natural killer T cells |
title_sort | peripheral differentiation of human natural killer t cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6767057/ https://www.ncbi.nlm.nih.gov/pubmed/30875134 http://dx.doi.org/10.1111/imcb.12248 |
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