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Cytomegalovirus infection in malignant pleural mesothelioma

Human cytomegalovirus (HCMV) is a highly prevalent herpes virus which persists as a latent infection and has been detected in several different tumor types. HCMV disease is rare but may occur in high-risk settings, often manifesting as a pulmonary infection. To date HCMV has not been investigated in...

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Autores principales: Hunter-Schlichting, DeVon, Kelsey, Karl T., Demmer, Ryan, Patel, Manish, Bueno, Raphael, Christensen, Brock, Fujioka, Naomi, Kolarseri, Deepa, Nelson, Heather H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360519/
https://www.ncbi.nlm.nih.gov/pubmed/34383785
http://dx.doi.org/10.1371/journal.pone.0254136
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author Hunter-Schlichting, DeVon
Kelsey, Karl T.
Demmer, Ryan
Patel, Manish
Bueno, Raphael
Christensen, Brock
Fujioka, Naomi
Kolarseri, Deepa
Nelson, Heather H.
author_facet Hunter-Schlichting, DeVon
Kelsey, Karl T.
Demmer, Ryan
Patel, Manish
Bueno, Raphael
Christensen, Brock
Fujioka, Naomi
Kolarseri, Deepa
Nelson, Heather H.
author_sort Hunter-Schlichting, DeVon
collection PubMed
description Human cytomegalovirus (HCMV) is a highly prevalent herpes virus which persists as a latent infection and has been detected in several different tumor types. HCMV disease is rare but may occur in high-risk settings, often manifesting as a pulmonary infection. To date HCMV has not been investigated in malignant pleural mesothelioma (MPM). In a consecutive case series of 144 MPM patients we evaluated two biomarkers of HCMV: IgG serostatus (defined as positive and negative) and DNAemia (>100 copies/mL of cell free HCMV DNA in serum). Approximately half of the MPM patient population was HCMV IgG seropositive (51%). HCMV DNAemia was highly prevalent (79%) in MPM and independent of IgG serostatus. DNAemia levels consistent with high level current infection (>1000 copies/mL serum) were present in 41% of patients. Neither IgG serostatus nor DNAemia were associated with patient survival. In tissues, we observed that HCMV DNA was present in 48% of tumors (n = 40) and only 29% of normal pleural tissue obtained from individuals without malignancy (n = 21). Our results suggest nearly half of MPM patients have a high level current HCMV infection at the time of treatment and that pleural tissue may be a reservoir for latent HCMV infection. These findings warrant further investigation to determine the full spectrum of pulmonary infections in MPM patients, and whether treatment for high level current HCMV infection may improve patient outcomes.
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spelling pubmed-83605192021-08-13 Cytomegalovirus infection in malignant pleural mesothelioma Hunter-Schlichting, DeVon Kelsey, Karl T. Demmer, Ryan Patel, Manish Bueno, Raphael Christensen, Brock Fujioka, Naomi Kolarseri, Deepa Nelson, Heather H. PLoS One Research Article Human cytomegalovirus (HCMV) is a highly prevalent herpes virus which persists as a latent infection and has been detected in several different tumor types. HCMV disease is rare but may occur in high-risk settings, often manifesting as a pulmonary infection. To date HCMV has not been investigated in malignant pleural mesothelioma (MPM). In a consecutive case series of 144 MPM patients we evaluated two biomarkers of HCMV: IgG serostatus (defined as positive and negative) and DNAemia (>100 copies/mL of cell free HCMV DNA in serum). Approximately half of the MPM patient population was HCMV IgG seropositive (51%). HCMV DNAemia was highly prevalent (79%) in MPM and independent of IgG serostatus. DNAemia levels consistent with high level current infection (>1000 copies/mL serum) were present in 41% of patients. Neither IgG serostatus nor DNAemia were associated with patient survival. In tissues, we observed that HCMV DNA was present in 48% of tumors (n = 40) and only 29% of normal pleural tissue obtained from individuals without malignancy (n = 21). Our results suggest nearly half of MPM patients have a high level current HCMV infection at the time of treatment and that pleural tissue may be a reservoir for latent HCMV infection. These findings warrant further investigation to determine the full spectrum of pulmonary infections in MPM patients, and whether treatment for high level current HCMV infection may improve patient outcomes. Public Library of Science 2021-08-12 /pmc/articles/PMC8360519/ /pubmed/34383785 http://dx.doi.org/10.1371/journal.pone.0254136 Text en © 2021 Hunter-Schlichting et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hunter-Schlichting, DeVon
Kelsey, Karl T.
Demmer, Ryan
Patel, Manish
Bueno, Raphael
Christensen, Brock
Fujioka, Naomi
Kolarseri, Deepa
Nelson, Heather H.
Cytomegalovirus infection in malignant pleural mesothelioma
title Cytomegalovirus infection in malignant pleural mesothelioma
title_full Cytomegalovirus infection in malignant pleural mesothelioma
title_fullStr Cytomegalovirus infection in malignant pleural mesothelioma
title_full_unstemmed Cytomegalovirus infection in malignant pleural mesothelioma
title_short Cytomegalovirus infection in malignant pleural mesothelioma
title_sort cytomegalovirus infection in malignant pleural mesothelioma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360519/
https://www.ncbi.nlm.nih.gov/pubmed/34383785
http://dx.doi.org/10.1371/journal.pone.0254136
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