Simultaneous Quantification of the 8 Human Herpesviruses in Allogeneic Hematopoietic Stem Cell Transplantation

BACKGROUNDHuman herpesviruses may cause severe complications after allogeneic hematopoietic stem cell transplantation (HSCT). However, the impact of some of these infections on transplant outcomes is still unclear. A prospective survey on the incidence and clinical features of herpesviruses infectio...

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Veröffentlicht in:Transplantation 2016-06, Vol.100 (6), p.1363-1370
Hauptverfasser: Gomes de Oliveira, Paulo Guilherme Alvarenga, Ueda, Miriam Yurika Hiramoto, Real, Juliana Monte, de Sá Moreira, Eloisa, Rodrigues de Oliveira, José Salvador, Gonçalves, Matheus Vescovi, Ginani, Valeria Cortez, de Oliveira Felix, Olga Margareth Wanderley, Seber, Adriana, Novis, Yana, Rocha, Vanderson, Granato, Celso Francisco Hernandes, Arrais-Rodrigues, Celso
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container_end_page 1370
container_issue 6
container_start_page 1363
container_title Transplantation
container_volume 100
creator Gomes de Oliveira, Paulo Guilherme Alvarenga
Ueda, Miriam Yurika Hiramoto
Real, Juliana Monte
de Sá Moreira, Eloisa
Rodrigues de Oliveira, José Salvador
Gonçalves, Matheus Vescovi
Ginani, Valeria Cortez
de Oliveira Felix, Olga Margareth Wanderley
Seber, Adriana
Novis, Yana
Rocha, Vanderson
Granato, Celso Francisco Hernandes
Arrais-Rodrigues, Celso
description BACKGROUNDHuman herpesviruses may cause severe complications after allogeneic hematopoietic stem cell transplantation (HSCT). However, the impact of some of these infections on transplant outcomes is still unclear. A prospective survey on the incidence and clinical features of herpesviruses infections after HSCT has not yet been conducted in Brazilian patients, and the impact of these infections on HSCT outcome remains unclear. METHODSWe prospectively analyzed the incidence of infection of the eight human herpesviruses simultaneously in 1 045 peripheral blood samples from 98 allogeneic HSCT recipients. Samples were collected weekly starting at the time of transplant until day +100. All herpesviruses were screened and quantified in plasma by quantitative real-time polymerase chain reaction. Median follow up time was 24 months. RESULTSThe incidences of infection for each herpesvirus were as followscytomegalovirus (CMV), 44%; human herpesvirus [HHV] 6, 18%; HHV8, 6%; Epstein-Barr virus, 3%; herpes simplex virus 1, 3%; varicella zoster virus, 3%; HHV7, 2%; and herpes simplex virus 2, 1%. The CMV infection was significantly more frequent among adults and was associated with a higher risk of developing acute graft-versus-host disease. The HHV6 infection was significantly more frequent after umbilical cord blood transplant and was associated with an increased risk of platelet engraftment failure. There was no significant impact of these infections on the other transplant outcomes. CONCLUSIONSHerpesviruses infections were uncommon after HSCT, except for CMV and HHV6, which, although relatively frequent, had no clinically relevant impact on the outcomes.
doi_str_mv 10.1097/TP.0000000000000986
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However, the impact of some of these infections on transplant outcomes is still unclear. A prospective survey on the incidence and clinical features of herpesviruses infections after HSCT has not yet been conducted in Brazilian patients, and the impact of these infections on HSCT outcome remains unclear. METHODSWe prospectively analyzed the incidence of infection of the eight human herpesviruses simultaneously in 1 045 peripheral blood samples from 98 allogeneic HSCT recipients. Samples were collected weekly starting at the time of transplant until day +100. All herpesviruses were screened and quantified in plasma by quantitative real-time polymerase chain reaction. Median follow up time was 24 months. RESULTSThe incidences of infection for each herpesvirus were as followscytomegalovirus (CMV), 44%; human herpesvirus [HHV] 6, 18%; HHV8, 6%; Epstein-Barr virus, 3%; herpes simplex virus 1, 3%; varicella zoster virus, 3%; HHV7, 2%; and herpes simplex virus 2, 1%. The CMV infection was significantly more frequent among adults and was associated with a higher risk of developing acute graft-versus-host disease. The HHV6 infection was significantly more frequent after umbilical cord blood transplant and was associated with an increased risk of platelet engraftment failure. There was no significant impact of these infections on the other transplant outcomes. CONCLUSIONSHerpesviruses infections were uncommon after HSCT, except for CMV and HHV6, which, although relatively frequent, had no clinically relevant impact on the outcomes.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/TP.0000000000000986</identifier><identifier>PMID: 26555946</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Adolescent ; Adult ; Aged ; Brazil ; Child ; Child, Preschool ; DNA, Viral - blood ; Female ; Hematologic Neoplasms - complications ; Hematologic Neoplasms - therapy ; Hematopoietic Stem Cell Transplantation - adverse effects ; Herpesviridae ; Herpesviridae Infections - complications ; Herpesviridae Infections - etiology ; Humans ; Incidence ; Male ; Middle Aged ; Polymerase Chain Reaction ; Prospective Studies ; Real-Time Polymerase Chain Reaction ; Risk ; Transplantation, Homologous - adverse effects ; Treatment Outcome ; Virus Activation ; Young Adult</subject><ispartof>Transplantation, 2016-06, Vol.100 (6), p.1363-1370</ispartof><rights>Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3536-4e608d2c2ba32d5c54de834c4e3cc44bdd5a91e5c611338e2ae01667d5ab1c073</citedby><cites>FETCH-LOGICAL-c3536-4e608d2c2ba32d5c54de834c4e3cc44bdd5a91e5c611338e2ae01667d5ab1c073</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26555946$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gomes de Oliveira, Paulo Guilherme Alvarenga</creatorcontrib><creatorcontrib>Ueda, Miriam Yurika Hiramoto</creatorcontrib><creatorcontrib>Real, Juliana Monte</creatorcontrib><creatorcontrib>de Sá Moreira, Eloisa</creatorcontrib><creatorcontrib>Rodrigues de Oliveira, José Salvador</creatorcontrib><creatorcontrib>Gonçalves, Matheus Vescovi</creatorcontrib><creatorcontrib>Ginani, Valeria Cortez</creatorcontrib><creatorcontrib>de Oliveira Felix, Olga Margareth Wanderley</creatorcontrib><creatorcontrib>Seber, Adriana</creatorcontrib><creatorcontrib>Novis, Yana</creatorcontrib><creatorcontrib>Rocha, Vanderson</creatorcontrib><creatorcontrib>Granato, Celso Francisco Hernandes</creatorcontrib><creatorcontrib>Arrais-Rodrigues, Celso</creatorcontrib><title>Simultaneous Quantification of the 8 Human Herpesviruses in Allogeneic Hematopoietic Stem Cell Transplantation</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>BACKGROUNDHuman herpesviruses may cause severe complications after allogeneic hematopoietic stem cell transplantation (HSCT). However, the impact of some of these infections on transplant outcomes is still unclear. A prospective survey on the incidence and clinical features of herpesviruses infections after HSCT has not yet been conducted in Brazilian patients, and the impact of these infections on HSCT outcome remains unclear. METHODSWe prospectively analyzed the incidence of infection of the eight human herpesviruses simultaneously in 1 045 peripheral blood samples from 98 allogeneic HSCT recipients. Samples were collected weekly starting at the time of transplant until day +100. All herpesviruses were screened and quantified in plasma by quantitative real-time polymerase chain reaction. Median follow up time was 24 months. RESULTSThe incidences of infection for each herpesvirus were as followscytomegalovirus (CMV), 44%; human herpesvirus [HHV] 6, 18%; HHV8, 6%; Epstein-Barr virus, 3%; herpes simplex virus 1, 3%; varicella zoster virus, 3%; HHV7, 2%; and herpes simplex virus 2, 1%. The CMV infection was significantly more frequent among adults and was associated with a higher risk of developing acute graft-versus-host disease. The HHV6 infection was significantly more frequent after umbilical cord blood transplant and was associated with an increased risk of platelet engraftment failure. There was no significant impact of these infections on the other transplant outcomes. CONCLUSIONSHerpesviruses infections were uncommon after HSCT, except for CMV and HHV6, which, although relatively frequent, had no clinically relevant impact on the outcomes.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Brazil</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>DNA, Viral - blood</subject><subject>Female</subject><subject>Hematologic Neoplasms - complications</subject><subject>Hematologic Neoplasms - therapy</subject><subject>Hematopoietic Stem Cell Transplantation - adverse effects</subject><subject>Herpesviridae</subject><subject>Herpesviridae Infections - complications</subject><subject>Herpesviridae Infections - etiology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Polymerase Chain Reaction</subject><subject>Prospective Studies</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Risk</subject><subject>Transplantation, Homologous - adverse effects</subject><subject>Treatment Outcome</subject><subject>Virus Activation</subject><subject>Young Adult</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EgvL4AiTkJZsUO34kWaIKKBISoJZ15DpTanDiYDtU_D2GAkIs8GZkz5k7vhehY0rGlFTF2fxuTH6fqpRbaEQF45kkJdlGI0I4zShjxR7aD-EpMYIVxS7ay6UQouJyhLqZaQcbVQduCPh-UF00S6NVNK7DbonjCnCJp0OrOjwF30N4NX4IELDp8Lm17hE6MDr1WhVd7wzEdJtFaPEErMVzr7rQ2yT7KXmIdpbKBjj6qgfo4fJiPplmN7dX15Pzm0wzwWTGITlocp0vFMsboQVvoGRcc2Bac75oGqEqCkJLmuyVkCsgVMoiPS-oJgU7QKcb3d67lwFCrFsTdPrQxmhNi4pwWeafKNug2rsQPCzr3ptW-beakvoj6Hp-V_8NOk2dfC0YFi00PzPfySag2ABrZyP48GyHNfh6BcrG1b_S79nKiyE</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Gomes de Oliveira, Paulo Guilherme Alvarenga</creator><creator>Ueda, Miriam Yurika Hiramoto</creator><creator>Real, Juliana Monte</creator><creator>de Sá Moreira, Eloisa</creator><creator>Rodrigues de Oliveira, José Salvador</creator><creator>Gonçalves, Matheus Vescovi</creator><creator>Ginani, Valeria Cortez</creator><creator>de Oliveira Felix, Olga Margareth Wanderley</creator><creator>Seber, Adriana</creator><creator>Novis, Yana</creator><creator>Rocha, Vanderson</creator><creator>Granato, Celso Francisco Hernandes</creator><creator>Arrais-Rodrigues, Celso</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201606</creationdate><title>Simultaneous Quantification of the 8 Human Herpesviruses in Allogeneic Hematopoietic Stem Cell Transplantation</title><author>Gomes de Oliveira, Paulo Guilherme Alvarenga ; Ueda, Miriam Yurika Hiramoto ; Real, Juliana Monte ; de Sá Moreira, Eloisa ; Rodrigues de Oliveira, José Salvador ; Gonçalves, Matheus Vescovi ; Ginani, Valeria Cortez ; de Oliveira Felix, Olga Margareth Wanderley ; Seber, Adriana ; Novis, Yana ; Rocha, Vanderson ; Granato, Celso Francisco Hernandes ; Arrais-Rodrigues, Celso</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-4e608d2c2ba32d5c54de834c4e3cc44bdd5a91e5c611338e2ae01667d5ab1c073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Brazil</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>DNA, Viral - blood</topic><topic>Female</topic><topic>Hematologic Neoplasms - complications</topic><topic>Hematologic Neoplasms - therapy</topic><topic>Hematopoietic Stem Cell Transplantation - adverse effects</topic><topic>Herpesviridae</topic><topic>Herpesviridae Infections - complications</topic><topic>Herpesviridae Infections - etiology</topic><topic>Humans</topic><topic>Incidence</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Polymerase Chain Reaction</topic><topic>Prospective Studies</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Risk</topic><topic>Transplantation, Homologous - adverse effects</topic><topic>Treatment Outcome</topic><topic>Virus Activation</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomes de Oliveira, Paulo Guilherme Alvarenga</creatorcontrib><creatorcontrib>Ueda, Miriam Yurika Hiramoto</creatorcontrib><creatorcontrib>Real, Juliana Monte</creatorcontrib><creatorcontrib>de Sá Moreira, Eloisa</creatorcontrib><creatorcontrib>Rodrigues de Oliveira, José Salvador</creatorcontrib><creatorcontrib>Gonçalves, Matheus Vescovi</creatorcontrib><creatorcontrib>Ginani, Valeria Cortez</creatorcontrib><creatorcontrib>de Oliveira Felix, Olga Margareth Wanderley</creatorcontrib><creatorcontrib>Seber, Adriana</creatorcontrib><creatorcontrib>Novis, Yana</creatorcontrib><creatorcontrib>Rocha, Vanderson</creatorcontrib><creatorcontrib>Granato, Celso Francisco Hernandes</creatorcontrib><creatorcontrib>Arrais-Rodrigues, Celso</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gomes de Oliveira, Paulo Guilherme Alvarenga</au><au>Ueda, Miriam Yurika Hiramoto</au><au>Real, Juliana Monte</au><au>de Sá Moreira, Eloisa</au><au>Rodrigues de Oliveira, José Salvador</au><au>Gonçalves, Matheus Vescovi</au><au>Ginani, Valeria Cortez</au><au>de Oliveira Felix, Olga Margareth Wanderley</au><au>Seber, Adriana</au><au>Novis, Yana</au><au>Rocha, Vanderson</au><au>Granato, Celso Francisco Hernandes</au><au>Arrais-Rodrigues, Celso</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Simultaneous Quantification of the 8 Human Herpesviruses in Allogeneic Hematopoietic Stem Cell Transplantation</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>2016-06</date><risdate>2016</risdate><volume>100</volume><issue>6</issue><spage>1363</spage><epage>1370</epage><pages>1363-1370</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><abstract>BACKGROUNDHuman herpesviruses may cause severe complications after allogeneic hematopoietic stem cell transplantation (HSCT). However, the impact of some of these infections on transplant outcomes is still unclear. A prospective survey on the incidence and clinical features of herpesviruses infections after HSCT has not yet been conducted in Brazilian patients, and the impact of these infections on HSCT outcome remains unclear. METHODSWe prospectively analyzed the incidence of infection of the eight human herpesviruses simultaneously in 1 045 peripheral blood samples from 98 allogeneic HSCT recipients. Samples were collected weekly starting at the time of transplant until day +100. All herpesviruses were screened and quantified in plasma by quantitative real-time polymerase chain reaction. Median follow up time was 24 months. RESULTSThe incidences of infection for each herpesvirus were as followscytomegalovirus (CMV), 44%; human herpesvirus [HHV] 6, 18%; HHV8, 6%; Epstein-Barr virus, 3%; herpes simplex virus 1, 3%; varicella zoster virus, 3%; HHV7, 2%; and herpes simplex virus 2, 1%. The CMV infection was significantly more frequent among adults and was associated with a higher risk of developing acute graft-versus-host disease. The HHV6 infection was significantly more frequent after umbilical cord blood transplant and was associated with an increased risk of platelet engraftment failure. There was no significant impact of these infections on the other transplant outcomes. CONCLUSIONSHerpesviruses infections were uncommon after HSCT, except for CMV and HHV6, which, although relatively frequent, had no clinically relevant impact on the outcomes.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>26555946</pmid><doi>10.1097/TP.0000000000000986</doi><tpages>8</tpages></addata></record>
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subjects Adolescent
Adult
Aged
Brazil
Child
Child, Preschool
DNA, Viral - blood
Female
Hematologic Neoplasms - complications
Hematologic Neoplasms - therapy
Hematopoietic Stem Cell Transplantation - adverse effects
Herpesviridae
Herpesviridae Infections - complications
Herpesviridae Infections - etiology
Humans
Incidence
Male
Middle Aged
Polymerase Chain Reaction
Prospective Studies
Real-Time Polymerase Chain Reaction
Risk
Transplantation, Homologous - adverse effects
Treatment Outcome
Virus Activation
Young Adult
title Simultaneous Quantification of the 8 Human Herpesviruses in Allogeneic Hematopoietic Stem Cell Transplantation
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