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CD8αα Expression Marks Terminally Differentiated Human CD8+ T Cells Expanded in Chronic Viral Infection

The T cell co-receptor CD8αβ enhances T cell sensitivity to antigen, however studies indicate CD8αα has the converse effect and acts as a co-repressor. Using a combination of Thymic Leukemia (TL) antigen tetramer, which directly binds CD8αα, anti-CD161, and anti-Vα7.2 antibodies we have been able fo...

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Autores principales: Walker, L. J., Marrinan, E., Muenchhoff, M., Ferguson, J., Kloverpris, H., Cheroutre, H., Barnes, E., Goulder, P., Klenerman, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734367/
https://www.ncbi.nlm.nih.gov/pubmed/23964274
http://dx.doi.org/10.3389/fimmu.2013.00223
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author Walker, L. J.
Marrinan, E.
Muenchhoff, M.
Ferguson, J.
Kloverpris, H.
Cheroutre, H.
Barnes, E.
Goulder, P.
Klenerman, Paul
author_facet Walker, L. J.
Marrinan, E.
Muenchhoff, M.
Ferguson, J.
Kloverpris, H.
Cheroutre, H.
Barnes, E.
Goulder, P.
Klenerman, Paul
author_sort Walker, L. J.
collection PubMed
description The T cell co-receptor CD8αβ enhances T cell sensitivity to antigen, however studies indicate CD8αα has the converse effect and acts as a co-repressor. Using a combination of Thymic Leukemia (TL) antigen tetramer, which directly binds CD8αα, anti-CD161, and anti-Vα7.2 antibodies we have been able for the first time to clearly define CD8αα expression on human CD8 T cells subsets. In healthy controls CD8αα is most highly expressed by CD161 “bright” (CD161++) mucosal associated invariant T (MAIT) cells, with CD8αα expression highly restricted to the TCR Vα7.2+ cells of this subset. We also identified CD8αα-expressing populations within the CD161 “mid” (CD161+) and “negative” (CD161−) non-MAIT CD8 T cell subsets and show TL-tetramer binding to correlate with expression of CD8β at low levels in the context of maintained CD8α expression (CD8α+CD8β(low)). In addition, we found CD161−CD8α+CD8β(low) populations to be significantly expanded in the peripheral blood of HIV-1 and hepatitis B (mean of 47 and 40% of CD161− T cells respectively) infected individuals. Such CD8αα expressing T cells are an effector-memory population (CD45RA−, CCR7−, CD62L−) that express markers of activation and maturation (HLA-DR+, CD28−, CD27−, CD57+) and are functionally distinct, expressing greater levels of TNF-α and IFN-γ on stimulation and perforin at rest than their CD8α+CD8β(high) counterparts. Antigen-specific T cells in HLA-B(∗)4201+HIV-1 infected patients are found within both the CD161−CD8α+CD8β(high) and CD161−CD8α+CD8β(low) populations. Overall we have clearly defined CD8αα expressing human T cell subsets using the TL-tetramer, and have demonstrated CD161−CD8α+CD8β(low) populations, highly expanded in disease settings, to co-express CD8αβ and CD8αα. Co-expression of CD8αα on CD8αβ T cells may impact on their overall function in vivo and contribute to the distinctive phenotype of highly differentiated populations in HBV and HIV-1 infection.
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spelling pubmed-37343672013-08-20 CD8αα Expression Marks Terminally Differentiated Human CD8+ T Cells Expanded in Chronic Viral Infection Walker, L. J. Marrinan, E. Muenchhoff, M. Ferguson, J. Kloverpris, H. Cheroutre, H. Barnes, E. Goulder, P. Klenerman, Paul Front Immunol Immunology The T cell co-receptor CD8αβ enhances T cell sensitivity to antigen, however studies indicate CD8αα has the converse effect and acts as a co-repressor. Using a combination of Thymic Leukemia (TL) antigen tetramer, which directly binds CD8αα, anti-CD161, and anti-Vα7.2 antibodies we have been able for the first time to clearly define CD8αα expression on human CD8 T cells subsets. In healthy controls CD8αα is most highly expressed by CD161 “bright” (CD161++) mucosal associated invariant T (MAIT) cells, with CD8αα expression highly restricted to the TCR Vα7.2+ cells of this subset. We also identified CD8αα-expressing populations within the CD161 “mid” (CD161+) and “negative” (CD161−) non-MAIT CD8 T cell subsets and show TL-tetramer binding to correlate with expression of CD8β at low levels in the context of maintained CD8α expression (CD8α+CD8β(low)). In addition, we found CD161−CD8α+CD8β(low) populations to be significantly expanded in the peripheral blood of HIV-1 and hepatitis B (mean of 47 and 40% of CD161− T cells respectively) infected individuals. Such CD8αα expressing T cells are an effector-memory population (CD45RA−, CCR7−, CD62L−) that express markers of activation and maturation (HLA-DR+, CD28−, CD27−, CD57+) and are functionally distinct, expressing greater levels of TNF-α and IFN-γ on stimulation and perforin at rest than their CD8α+CD8β(high) counterparts. Antigen-specific T cells in HLA-B(∗)4201+HIV-1 infected patients are found within both the CD161−CD8α+CD8β(high) and CD161−CD8α+CD8β(low) populations. Overall we have clearly defined CD8αα expressing human T cell subsets using the TL-tetramer, and have demonstrated CD161−CD8α+CD8β(low) populations, highly expanded in disease settings, to co-express CD8αβ and CD8αα. Co-expression of CD8αα on CD8αβ T cells may impact on their overall function in vivo and contribute to the distinctive phenotype of highly differentiated populations in HBV and HIV-1 infection. Frontiers Media S.A. 2013-08-06 /pmc/articles/PMC3734367/ /pubmed/23964274 http://dx.doi.org/10.3389/fimmu.2013.00223 Text en Copyright © 2013 Walker, Marrinan, Muenchhoff, Ferguson, Kloverpris, Cheroutre, Barnes, Goulder and Klenerman. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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
Walker, L. J.
Marrinan, E.
Muenchhoff, M.
Ferguson, J.
Kloverpris, H.
Cheroutre, H.
Barnes, E.
Goulder, P.
Klenerman, Paul
CD8αα Expression Marks Terminally Differentiated Human CD8+ T Cells Expanded in Chronic Viral Infection
title CD8αα Expression Marks Terminally Differentiated Human CD8+ T Cells Expanded in Chronic Viral Infection
title_full CD8αα Expression Marks Terminally Differentiated Human CD8+ T Cells Expanded in Chronic Viral Infection
title_fullStr CD8αα Expression Marks Terminally Differentiated Human CD8+ T Cells Expanded in Chronic Viral Infection
title_full_unstemmed CD8αα Expression Marks Terminally Differentiated Human CD8+ T Cells Expanded in Chronic Viral Infection
title_short CD8αα Expression Marks Terminally Differentiated Human CD8+ T Cells Expanded in Chronic Viral Infection
title_sort cd8αα expression marks terminally differentiated human cd8+ t cells expanded in chronic viral infection
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734367/
https://www.ncbi.nlm.nih.gov/pubmed/23964274
http://dx.doi.org/10.3389/fimmu.2013.00223
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