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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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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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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0254136</identifier><identifier>PMID: 34383785</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Age ; Aged ; Antibodies, Viral - blood ; Asbestos ; Biobanks ; Biology and life sciences ; Biomarkers ; Complications and side effects ; Consent ; Cytomegalovirus ; Cytomegalovirus - metabolism ; Cytomegalovirus infections ; Cytomegalovirus Infections - blood ; Cytomegalovirus Infections - mortality ; Deoxyribonucleic acid ; Diagnosis ; Disease-Free Survival ; DNA ; DNA, Viral - blood ; Epidemiology ; Female ; Hematology ; Histology ; Hospitals ; Humans ; Immunoglobulin G ; Immunoglobulin G - blood ; Infections ; Laboratories ; Latent infection ; Lung cancer ; Male ; Malignancy ; Medical prognosis ; Medicine and Health Sciences ; Mesothelioma ; Mesothelioma, Malignant - blood ; Mesothelioma, Malignant - mortality ; Mesothelioma, Malignant - virology ; Metastasis ; Middle Aged ; Pathology ; Patients ; Pleural Neoplasms - blood ; Pleural Neoplasms - mortality ; Pleural Neoplasms - virology ; Pneumonia ; Pneumonia, Viral - blood ; Pneumonia, Viral - mortality ; Pneumonia, Viral - virology ; Prognosis ; Questionnaires ; Retrospective Studies ; Risk factors ; Serology ; Survival Rate ; Thoracic surgery ; Tissues ; Transplants & implants ; Tumors ; Viral infections ; Viruses ; Womens health</subject><ispartof>PloS one, 2021-08, Vol.16 (8), p.e0254136-e0254136</ispartof><rights>COPYRIGHT 2021 Public Library of Science</rights><rights>2021 Hunter-Schlichting et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 Hunter-Schlichting et al 2021 Hunter-Schlichting et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-b9c34500ab5cdfcb906714e7a6599ce5b0e4dcbc0df9f60a6b8130b12c1e486f3</citedby><cites>FETCH-LOGICAL-c692t-b9c34500ab5cdfcb906714e7a6599ce5b0e4dcbc0df9f60a6b8130b12c1e486f3</cites><orcidid>0000-0002-3231-5491 ; 0000-0002-2986-9602</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360519/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8360519/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,2096,2915,23847,27905,27906,53772,53774,79349,79350</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34383785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Spencer, Juliet V.</contributor><creatorcontrib>Hunter-Schlichting, DeVon</creatorcontrib><creatorcontrib>Kelsey, Karl T</creatorcontrib><creatorcontrib>Demmer, Ryan</creatorcontrib><creatorcontrib>Patel, Manish</creatorcontrib><creatorcontrib>Bueno, Raphael</creatorcontrib><creatorcontrib>Christensen, Brock</creatorcontrib><creatorcontrib>Fujioka, Naomi</creatorcontrib><creatorcontrib>Kolarseri, Deepa</creatorcontrib><creatorcontrib>Nelson, Heather H</creatorcontrib><title>Cytomegalovirus infection in malignant pleural mesothelioma</title><title>PloS one</title><addtitle>PLoS One</addtitle><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. 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Brock</au><au>Fujioka, Naomi</au><au>Kolarseri, Deepa</au><au>Nelson, Heather H</au><au>Spencer, Juliet V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytomegalovirus infection in malignant pleural mesothelioma</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2021-08-12</date><risdate>2021</risdate><volume>16</volume><issue>8</issue><spage>e0254136</spage><epage>e0254136</epage><pages>e0254136-e0254136</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>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.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>34383785</pmid><doi>10.1371/journal.pone.0254136</doi><tpages>e0254136</tpages><orcidid>https://orcid.org/0000-0002-3231-5491</orcidid><orcidid>https://orcid.org/0000-0002-2986-9602</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
recordid | cdi_plos_journals_2560814397 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS); PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Age Aged Antibodies, Viral - blood Asbestos Biobanks Biology and life sciences Biomarkers Complications and side effects Consent Cytomegalovirus Cytomegalovirus - metabolism Cytomegalovirus infections Cytomegalovirus Infections - blood Cytomegalovirus Infections - mortality Deoxyribonucleic acid Diagnosis Disease-Free Survival DNA DNA, Viral - blood Epidemiology Female Hematology Histology Hospitals Humans Immunoglobulin G Immunoglobulin G - blood Infections Laboratories Latent infection Lung cancer Male Malignancy Medical prognosis Medicine and Health Sciences Mesothelioma Mesothelioma, Malignant - blood Mesothelioma, Malignant - mortality Mesothelioma, Malignant - virology Metastasis Middle Aged Pathology Patients Pleural Neoplasms - blood Pleural Neoplasms - mortality Pleural Neoplasms - virology Pneumonia Pneumonia, Viral - blood Pneumonia, Viral - mortality Pneumonia, Viral - virology Prognosis Questionnaires Retrospective Studies Risk factors Serology Survival Rate Thoracic surgery Tissues Transplants & implants Tumors Viral infections Viruses Womens health |
title | Cytomegalovirus infection in malignant pleural mesothelioma |
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