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Heterogeneity and Breadth of Host Antibody Response to KSHV Infection Demonstrated by Systematic Analysis of the KSHV Proteome

The Kaposi sarcoma associated herpesvirus (KSHV) genome encodes more than 85 open reading frames (ORFs). Serological evaluation of KSHV infection now generally relies on reactivity to just one latent and/or one lytic protein (commonly ORF73 and K8.1). Most of the other polypeptides encoded by the vi...

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Autores principales: Labo, Nazzarena, Miley, Wendell, Marshall, Vickie, Gillette, William, Esposito, Dominic, Bess, Matthew, Turano, Alexandra, Uldrick, Thomas, Polizzotto, Mark N., Wyvill, Kathleen M., Bagni, Rachel, Yarchoan, Robert, Whitby, Denise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968157/
https://www.ncbi.nlm.nih.gov/pubmed/24675986
http://dx.doi.org/10.1371/journal.ppat.1004046
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author Labo, Nazzarena
Miley, Wendell
Marshall, Vickie
Gillette, William
Esposito, Dominic
Bess, Matthew
Turano, Alexandra
Uldrick, Thomas
Polizzotto, Mark N.
Wyvill, Kathleen M.
Bagni, Rachel
Yarchoan, Robert
Whitby, Denise
author_facet Labo, Nazzarena
Miley, Wendell
Marshall, Vickie
Gillette, William
Esposito, Dominic
Bess, Matthew
Turano, Alexandra
Uldrick, Thomas
Polizzotto, Mark N.
Wyvill, Kathleen M.
Bagni, Rachel
Yarchoan, Robert
Whitby, Denise
author_sort Labo, Nazzarena
collection PubMed
description The Kaposi sarcoma associated herpesvirus (KSHV) genome encodes more than 85 open reading frames (ORFs). Serological evaluation of KSHV infection now generally relies on reactivity to just one latent and/or one lytic protein (commonly ORF73 and K8.1). Most of the other polypeptides encoded by the virus have unknown antigenic profiles. We have systematically expressed and purified products from 72 KSHV ORFs in recombinant systems and analyzed seroreactivity in US patients with KSHV-associated malignancies, and US blood donors (low KSHV seroprevalence population). We identified several KSHV proteins (ORF38, ORF61, ORF59 and K5) that elicited significant responses in individuals with KSHV-associated diseases. In these patients, patterns of reactivity were heterogeneous; however, HIV infection appeared to be associated with breadth and intensity of serological responses. Improved antigenic characterization of additional ORFs may increase the sensitivity of serologic assays, lead to more rapid progresses in understanding immune responses to KSHV, and allow for better comprehension of the natural history of KSHV infection. To this end, we have developed a bead-based multiplex assay detecting antibodies to six KSHV antigens.
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spelling pubmed-39681572014-04-01 Heterogeneity and Breadth of Host Antibody Response to KSHV Infection Demonstrated by Systematic Analysis of the KSHV Proteome Labo, Nazzarena Miley, Wendell Marshall, Vickie Gillette, William Esposito, Dominic Bess, Matthew Turano, Alexandra Uldrick, Thomas Polizzotto, Mark N. Wyvill, Kathleen M. Bagni, Rachel Yarchoan, Robert Whitby, Denise PLoS Pathog Research Article The Kaposi sarcoma associated herpesvirus (KSHV) genome encodes more than 85 open reading frames (ORFs). Serological evaluation of KSHV infection now generally relies on reactivity to just one latent and/or one lytic protein (commonly ORF73 and K8.1). Most of the other polypeptides encoded by the virus have unknown antigenic profiles. We have systematically expressed and purified products from 72 KSHV ORFs in recombinant systems and analyzed seroreactivity in US patients with KSHV-associated malignancies, and US blood donors (low KSHV seroprevalence population). We identified several KSHV proteins (ORF38, ORF61, ORF59 and K5) that elicited significant responses in individuals with KSHV-associated diseases. In these patients, patterns of reactivity were heterogeneous; however, HIV infection appeared to be associated with breadth and intensity of serological responses. Improved antigenic characterization of additional ORFs may increase the sensitivity of serologic assays, lead to more rapid progresses in understanding immune responses to KSHV, and allow for better comprehension of the natural history of KSHV infection. To this end, we have developed a bead-based multiplex assay detecting antibodies to six KSHV antigens. Public Library of Science 2014-03-27 /pmc/articles/PMC3968157/ /pubmed/24675986 http://dx.doi.org/10.1371/journal.ppat.1004046 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Labo, Nazzarena
Miley, Wendell
Marshall, Vickie
Gillette, William
Esposito, Dominic
Bess, Matthew
Turano, Alexandra
Uldrick, Thomas
Polizzotto, Mark N.
Wyvill, Kathleen M.
Bagni, Rachel
Yarchoan, Robert
Whitby, Denise
Heterogeneity and Breadth of Host Antibody Response to KSHV Infection Demonstrated by Systematic Analysis of the KSHV Proteome
title Heterogeneity and Breadth of Host Antibody Response to KSHV Infection Demonstrated by Systematic Analysis of the KSHV Proteome
title_full Heterogeneity and Breadth of Host Antibody Response to KSHV Infection Demonstrated by Systematic Analysis of the KSHV Proteome
title_fullStr Heterogeneity and Breadth of Host Antibody Response to KSHV Infection Demonstrated by Systematic Analysis of the KSHV Proteome
title_full_unstemmed Heterogeneity and Breadth of Host Antibody Response to KSHV Infection Demonstrated by Systematic Analysis of the KSHV Proteome
title_short Heterogeneity and Breadth of Host Antibody Response to KSHV Infection Demonstrated by Systematic Analysis of the KSHV Proteome
title_sort heterogeneity and breadth of host antibody response to kshv infection demonstrated by systematic analysis of the kshv proteome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3968157/
https://www.ncbi.nlm.nih.gov/pubmed/24675986
http://dx.doi.org/10.1371/journal.ppat.1004046
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