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CD161(int) CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut

The C-type lectin-like receptor CD161 is expressed on lymphocytes found in human gut and liver, as well as blood, especially Natural Killer cells, T helper 17 cells and a population of unconventional T cells known as Mucosal Associated Invariant T (MAIT) cells. The association of high CD161 expressi...

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Autores principales: Fergusson, J.R., Hühn, M.H., Swadling, L., Walker, L.J., Kurioka, A., Llibre, A., Bertoletti, A., Holländer, G., Newell, E.W., Davis, M.M., Sverremark-Ekström, E., Powrie, F., Capone, S., Folgori, A., Barnes, E., Willberg, C.B., Ussher, J.E., Klenerman, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732939/
https://www.ncbi.nlm.nih.gov/pubmed/26220166
http://dx.doi.org/10.1038/mi.2015.69
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author Fergusson, J.R.
Hühn, M.H.
Swadling, L.
Walker, L.J.
Kurioka, A.
Llibre, A.
Bertoletti, A.
Holländer, G.
Newell, E.W.
Davis, M.M.
Sverremark-Ekström, E.
Powrie, F.
Capone, S.
Folgori, A.
Barnes, E.
Willberg, C.B.
Ussher, J.E.
Klenerman, P.
author_facet Fergusson, J.R.
Hühn, M.H.
Swadling, L.
Walker, L.J.
Kurioka, A.
Llibre, A.
Bertoletti, A.
Holländer, G.
Newell, E.W.
Davis, M.M.
Sverremark-Ekström, E.
Powrie, F.
Capone, S.
Folgori, A.
Barnes, E.
Willberg, C.B.
Ussher, J.E.
Klenerman, P.
author_sort Fergusson, J.R.
collection PubMed
description The C-type lectin-like receptor CD161 is expressed on lymphocytes found in human gut and liver, as well as blood, especially Natural Killer cells, T helper 17 cells and a population of unconventional T cells known as Mucosal Associated Invariant T (MAIT) cells. The association of high CD161 expression with innate T cell populations including MAIT cells is established. Here we show that CD161 is also expressed, at intermediate levels, on a prominent subset of polyclonal CD8+ T cells, including anti-viral populations, which display a memory phenotype. These memory CD161(int) CD8+ T cells are enriched within the colon and express both CD103 and CD69, markers associated with tissue residence. Furthermore, this population was characterised by enhanced polyfunctionality, increased levels of cytotoxic mediators and high expression of the transcription factors T-bet and Eomesodermin. Such populations were induced by novel vaccine strategies based on adenoviral vectors, currently in trial against Hepatitis C virus. Thus, intermediate CD161 expression marks potent polyclonal, polyfunctional tissue-homing CD8+ T cell populations in humans. Since induction of such responses represents a major aim of T cell prophylactic and therapeutic vaccines in viral disease and cancer, analysis of these populations could be of value in the future.
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spelling pubmed-47329392016-05-18 CD161(int) CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut Fergusson, J.R. Hühn, M.H. Swadling, L. Walker, L.J. Kurioka, A. Llibre, A. Bertoletti, A. Holländer, G. Newell, E.W. Davis, M.M. Sverremark-Ekström, E. Powrie, F. Capone, S. Folgori, A. Barnes, E. Willberg, C.B. Ussher, J.E. Klenerman, P. Mucosal Immunol Article The C-type lectin-like receptor CD161 is expressed on lymphocytes found in human gut and liver, as well as blood, especially Natural Killer cells, T helper 17 cells and a population of unconventional T cells known as Mucosal Associated Invariant T (MAIT) cells. The association of high CD161 expression with innate T cell populations including MAIT cells is established. Here we show that CD161 is also expressed, at intermediate levels, on a prominent subset of polyclonal CD8+ T cells, including anti-viral populations, which display a memory phenotype. These memory CD161(int) CD8+ T cells are enriched within the colon and express both CD103 and CD69, markers associated with tissue residence. Furthermore, this population was characterised by enhanced polyfunctionality, increased levels of cytotoxic mediators and high expression of the transcription factors T-bet and Eomesodermin. Such populations were induced by novel vaccine strategies based on adenoviral vectors, currently in trial against Hepatitis C virus. Thus, intermediate CD161 expression marks potent polyclonal, polyfunctional tissue-homing CD8+ T cell populations in humans. Since induction of such responses represents a major aim of T cell prophylactic and therapeutic vaccines in viral disease and cancer, analysis of these populations could be of value in the future. 2015-07-29 2016-03 /pmc/articles/PMC4732939/ /pubmed/26220166 http://dx.doi.org/10.1038/mi.2015.69 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Fergusson, J.R.
Hühn, M.H.
Swadling, L.
Walker, L.J.
Kurioka, A.
Llibre, A.
Bertoletti, A.
Holländer, G.
Newell, E.W.
Davis, M.M.
Sverremark-Ekström, E.
Powrie, F.
Capone, S.
Folgori, A.
Barnes, E.
Willberg, C.B.
Ussher, J.E.
Klenerman, P.
CD161(int) CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut
title CD161(int) CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut
title_full CD161(int) CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut
title_fullStr CD161(int) CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut
title_full_unstemmed CD161(int) CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut
title_short CD161(int) CD8+ T cells: a novel population of highly functional, memory CD8+ T cells enriched within the gut
title_sort cd161(int) cd8+ t cells: a novel population of highly functional, memory cd8+ t cells enriched within the gut
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732939/
https://www.ncbi.nlm.nih.gov/pubmed/26220166
http://dx.doi.org/10.1038/mi.2015.69
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