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High Frequency, Sustained T Cell Responses to PARV4 Suggest Viral Persistence In Vivo
Background. Parvovirus 4 (PARV4) is a recently identified human virus that has been found in livers of patients infected with hepatitis C virus (HCV) and in bone marrow of individuals infected with human immunodeficiency virus (HIV). T cells are important in controlling viruses but may also contribu...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080894/ https://www.ncbi.nlm.nih.gov/pubmed/21502079 http://dx.doi.org/10.1093/infdis/jir036 |
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author | Simmons, Ruth Sharp, Colin Sims, Stuart Kloverpris, Henrik Goulder, Philip Simmonds, Peter Bowness, Paul Klenerman, Paul |
author_facet | Simmons, Ruth Sharp, Colin Sims, Stuart Kloverpris, Henrik Goulder, Philip Simmonds, Peter Bowness, Paul Klenerman, Paul |
author_sort | Simmons, Ruth |
collection | PubMed |
description | Background. Parvovirus 4 (PARV4) is a recently identified human virus that has been found in livers of patients infected with hepatitis C virus (HCV) and in bone marrow of individuals infected with human immunodeficiency virus (HIV). T cells are important in controlling viruses but may also contribute to disease pathogenesis. The interaction of PARV4 with the cellular immune system has not been described. Consequently, we investigated whether T cell responses to PARV4 could be detected in individuals exposed to blood-borne viruses. Methods. Interferon γ (IFN-γ) enzyme-linked immunospot assay, intracellular cytokine staining, and a tetrameric HLA-A*0201–peptide complex were used to define the lymphocyte populations responding to PARV4 NS peptides in 88 HCV-positive and 13 HIV-positive individuals. Antibody responses were tested using a recently developed PARV4 enzyme-linked immunosorbent assay. Results. High-frequency T cell responses against multiple PARV4 NS peptides and antibodies were observed in 26% of individuals. Typical responses to the NS pools were >1000 spot-forming units per million peripheral blood mononuclear cells. Conclusions. PARV4 infection is common in individuals exposed to blood-borne viruses and elicits strong T cell responses, a feature typically associated with persistent, contained infections such as cytomegalovirus. Persistence of PARV4 viral antigen in tissue in HCV-positive and HIV-positive individuals and/or the associated activated antiviral T cell response may contribute to disease pathogenesis. |
format | Text |
id | pubmed-3080894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-30808942011-05-15 High Frequency, Sustained T Cell Responses to PARV4 Suggest Viral Persistence In Vivo Simmons, Ruth Sharp, Colin Sims, Stuart Kloverpris, Henrik Goulder, Philip Simmonds, Peter Bowness, Paul Klenerman, Paul J Infect Dis Major Articles and Brief Reports Background. Parvovirus 4 (PARV4) is a recently identified human virus that has been found in livers of patients infected with hepatitis C virus (HCV) and in bone marrow of individuals infected with human immunodeficiency virus (HIV). T cells are important in controlling viruses but may also contribute to disease pathogenesis. The interaction of PARV4 with the cellular immune system has not been described. Consequently, we investigated whether T cell responses to PARV4 could be detected in individuals exposed to blood-borne viruses. Methods. Interferon γ (IFN-γ) enzyme-linked immunospot assay, intracellular cytokine staining, and a tetrameric HLA-A*0201–peptide complex were used to define the lymphocyte populations responding to PARV4 NS peptides in 88 HCV-positive and 13 HIV-positive individuals. Antibody responses were tested using a recently developed PARV4 enzyme-linked immunosorbent assay. Results. High-frequency T cell responses against multiple PARV4 NS peptides and antibodies were observed in 26% of individuals. Typical responses to the NS pools were >1000 spot-forming units per million peripheral blood mononuclear cells. Conclusions. PARV4 infection is common in individuals exposed to blood-borne viruses and elicits strong T cell responses, a feature typically associated with persistent, contained infections such as cytomegalovirus. Persistence of PARV4 viral antigen in tissue in HCV-positive and HIV-positive individuals and/or the associated activated antiviral T cell response may contribute to disease pathogenesis. Oxford University Press 2011-05-15 /pmc/articles/PMC3080894/ /pubmed/21502079 http://dx.doi.org/10.1093/infdis/jir036 Text en © The Author 2011. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Major Articles and Brief Reports Simmons, Ruth Sharp, Colin Sims, Stuart Kloverpris, Henrik Goulder, Philip Simmonds, Peter Bowness, Paul Klenerman, Paul High Frequency, Sustained T Cell Responses to PARV4 Suggest Viral Persistence In Vivo |
title | High Frequency, Sustained T Cell Responses to PARV4 Suggest Viral Persistence In Vivo |
title_full | High Frequency, Sustained T Cell Responses to PARV4 Suggest Viral Persistence In Vivo |
title_fullStr | High Frequency, Sustained T Cell Responses to PARV4 Suggest Viral Persistence In Vivo |
title_full_unstemmed | High Frequency, Sustained T Cell Responses to PARV4 Suggest Viral Persistence In Vivo |
title_short | High Frequency, Sustained T Cell Responses to PARV4 Suggest Viral Persistence In Vivo |
title_sort | high frequency, sustained t cell responses to parv4 suggest viral persistence in vivo |
topic | Major Articles and Brief Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3080894/ https://www.ncbi.nlm.nih.gov/pubmed/21502079 http://dx.doi.org/10.1093/infdis/jir036 |
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