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Broadly targeted human cytomegalovirus-specific CD4(+) and CD8(+) T cells dominate the memory compartments of exposed subjects

Human cytomegalovirus (HCMV) infections of immunocompetent hosts are characterized by a dynamic, life-long interaction in which host immune responses, particularly of T cells, restrain viral replication and prevent disease but do not eliminate the virus or preclude transmission. Because HCMV is amon...

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Autores principales: Sylwester, Andrew W., Mitchell, Bridget L., Edgar, John B., Taormina, Cara, Pelte, Christian, Ruchti, Franziska, Sleath, Paul R., Grabstein, Kenneth H., Hosken, Nancy A., Kern, Florian, Nelson, Jay A., Picker, Louis J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212883/
https://www.ncbi.nlm.nih.gov/pubmed/16147978
http://dx.doi.org/10.1084/jem.20050882
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author Sylwester, Andrew W.
Mitchell, Bridget L.
Edgar, John B.
Taormina, Cara
Pelte, Christian
Ruchti, Franziska
Sleath, Paul R.
Grabstein, Kenneth H.
Hosken, Nancy A.
Kern, Florian
Nelson, Jay A.
Picker, Louis J.
author_facet Sylwester, Andrew W.
Mitchell, Bridget L.
Edgar, John B.
Taormina, Cara
Pelte, Christian
Ruchti, Franziska
Sleath, Paul R.
Grabstein, Kenneth H.
Hosken, Nancy A.
Kern, Florian
Nelson, Jay A.
Picker, Louis J.
author_sort Sylwester, Andrew W.
collection PubMed
description Human cytomegalovirus (HCMV) infections of immunocompetent hosts are characterized by a dynamic, life-long interaction in which host immune responses, particularly of T cells, restrain viral replication and prevent disease but do not eliminate the virus or preclude transmission. Because HCMV is among the largest and most complex of known viruses, the T cell resources committed to maintaining this balance have never been characterized completely. Here, using cytokine flow cytometry and 13,687 overlapping 15mer peptides comprising 213 HCMV open reading frames (ORFs), we found that 151 HCMV ORFs were immunogenic for CD4(+) and/or CD8(+) T cells, and that ORF immunogenicity was influenced only modestly by ORF expression kinetics and function. We further documented that total HCMV-specific T cell responses in seropositive subjects were enormous, comprising on average ∼10% of both the CD4(+) and CD8(+) memory compartments in blood, whereas cross-reactive recognition of HCMV proteins in seronegative individuals was limited to CD8(+) T cells and was rare. These data provide the first glimpse of the total human T cell response to a complex infectious agent and will provide insight into the rules governing immunodominance and cross-reactivity in complex viral infections of humans.
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spelling pubmed-22128832008-03-11 Broadly targeted human cytomegalovirus-specific CD4(+) and CD8(+) T cells dominate the memory compartments of exposed subjects Sylwester, Andrew W. Mitchell, Bridget L. Edgar, John B. Taormina, Cara Pelte, Christian Ruchti, Franziska Sleath, Paul R. Grabstein, Kenneth H. Hosken, Nancy A. Kern, Florian Nelson, Jay A. Picker, Louis J. J Exp Med Article Human cytomegalovirus (HCMV) infections of immunocompetent hosts are characterized by a dynamic, life-long interaction in which host immune responses, particularly of T cells, restrain viral replication and prevent disease but do not eliminate the virus or preclude transmission. Because HCMV is among the largest and most complex of known viruses, the T cell resources committed to maintaining this balance have never been characterized completely. Here, using cytokine flow cytometry and 13,687 overlapping 15mer peptides comprising 213 HCMV open reading frames (ORFs), we found that 151 HCMV ORFs were immunogenic for CD4(+) and/or CD8(+) T cells, and that ORF immunogenicity was influenced only modestly by ORF expression kinetics and function. We further documented that total HCMV-specific T cell responses in seropositive subjects were enormous, comprising on average ∼10% of both the CD4(+) and CD8(+) memory compartments in blood, whereas cross-reactive recognition of HCMV proteins in seronegative individuals was limited to CD8(+) T cells and was rare. These data provide the first glimpse of the total human T cell response to a complex infectious agent and will provide insight into the rules governing immunodominance and cross-reactivity in complex viral infections of humans. The Rockefeller University Press 2005-09-05 /pmc/articles/PMC2212883/ /pubmed/16147978 http://dx.doi.org/10.1084/jem.20050882 Text en Copyright © 2005, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Sylwester, Andrew W.
Mitchell, Bridget L.
Edgar, John B.
Taormina, Cara
Pelte, Christian
Ruchti, Franziska
Sleath, Paul R.
Grabstein, Kenneth H.
Hosken, Nancy A.
Kern, Florian
Nelson, Jay A.
Picker, Louis J.
Broadly targeted human cytomegalovirus-specific CD4(+) and CD8(+) T cells dominate the memory compartments of exposed subjects
title Broadly targeted human cytomegalovirus-specific CD4(+) and CD8(+) T cells dominate the memory compartments of exposed subjects
title_full Broadly targeted human cytomegalovirus-specific CD4(+) and CD8(+) T cells dominate the memory compartments of exposed subjects
title_fullStr Broadly targeted human cytomegalovirus-specific CD4(+) and CD8(+) T cells dominate the memory compartments of exposed subjects
title_full_unstemmed Broadly targeted human cytomegalovirus-specific CD4(+) and CD8(+) T cells dominate the memory compartments of exposed subjects
title_short Broadly targeted human cytomegalovirus-specific CD4(+) and CD8(+) T cells dominate the memory compartments of exposed subjects
title_sort broadly targeted human cytomegalovirus-specific cd4(+) and cd8(+) t cells dominate the memory compartments of exposed subjects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212883/
https://www.ncbi.nlm.nih.gov/pubmed/16147978
http://dx.doi.org/10.1084/jem.20050882
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