Rotavirus vaccines: viral shedding and risk of transmission

Summary Rotavirus causes gastroenteritis in almost all children by 5 years of age. Immunity to rotavirus is incomplete, with potential for recurrent infections occurring throughout life. Live rotavirus vaccines have been developed for the protection of children from severe wildtype rotavirus infecti...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The Lancet infectious diseases 2008-10, Vol.8 (10), p.642-649
1. Verfasser: Anderson, Evan J, Dr
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 649
container_issue 10
container_start_page 642
container_title The Lancet infectious diseases
container_volume 8
creator Anderson, Evan J, Dr
description Summary Rotavirus causes gastroenteritis in almost all children by 5 years of age. Immunity to rotavirus is incomplete, with potential for recurrent infections occurring throughout life. Live rotavirus vaccines have been developed for the protection of children from severe wildtype rotavirus infections. Transmission of vaccine virus strains from vaccinated children to unvaccinated contacts harbours the potential for herd immunity, but also the risk of vaccine-derived disease in immunocompromised contacts. A review of rotavirus vaccine prelicensure studies shows that viral shedding and transmission were higher with the old tetravalent rhesus rotavirus vaccine than with the current human attenuated monovalent rotavirus vaccine and the pentavalent bovine-human reassortant vaccine. Immunocompromised contacts should be advised to avoid contact with stool from the immunised child if possible, particularly after the first vaccine dose for at least 14 days. Since the risk of vaccine transmission and subsequent vaccine-derived disease with the current vaccines is much less than the risk of wildtype rotavirus disease in immunocompromised contacts, vaccination should be encouraged.
doi_str_mv 10.1016/S1473-3099(08)70231-7
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69678240</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1473309908702317</els_id><sourcerecordid>69678240</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-5ba2c75f910bbd929036df87a13c74f5d0b740d16c86db28162c9fe105692d2f3</originalsourceid><addsrcrecordid>eNqFkFtrFTEURgdRbK3-BGUQFH0Y3cnkqqBI8QYFwctzyOSiaedk2uyZA_335pw5VOiLT7mw9pcvq2keE3hFgIjXPwiTfdeD1i9AvZRAe9LJO81xvWYdY1ze3e9X5Kh5gHgOQCQBdr85IkpTypQ4bt5-n2a7TWXBdmudSzngm7ae7djin-B9yr9bm31bEl60U2znYjNuEmKa8sPmXrQjhkeH9aT59enjz9Mv3dm3z19PP5x1jkk-d3yw1EkeNYFh8Jpq6IWPSlrSO8ki9zBIBp4Ip4QfqCKCOh0DAS409TT2J83zNfeyTFdLwNnUAi6Mo81hWtAILaSiDCr49BZ4Pi0l126GAuGCVTcV4ivkyoRYQjSXJW1suTYEzE6t2as1O28GlNmrNbLOPTmEL8Mm-H9TB5cVeHYALDo7xmrKJbzhKAjOtdhx71cuVGfbFIpBl0J2wacS3Gz8lP5b5d2tBDemnOqjF-E64M2niUFqYA3ZZYDaJ8j-Ly4tqLo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>201564474</pqid></control><display><type>article</type><title>Rotavirus vaccines: viral shedding and risk of transmission</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><source>ProQuest Central UK/Ireland</source><creator>Anderson, Evan J, Dr</creator><creatorcontrib>Anderson, Evan J, Dr</creatorcontrib><description>Summary Rotavirus causes gastroenteritis in almost all children by 5 years of age. Immunity to rotavirus is incomplete, with potential for recurrent infections occurring throughout life. Live rotavirus vaccines have been developed for the protection of children from severe wildtype rotavirus infections. Transmission of vaccine virus strains from vaccinated children to unvaccinated contacts harbours the potential for herd immunity, but also the risk of vaccine-derived disease in immunocompromised contacts. A review of rotavirus vaccine prelicensure studies shows that viral shedding and transmission were higher with the old tetravalent rhesus rotavirus vaccine than with the current human attenuated monovalent rotavirus vaccine and the pentavalent bovine-human reassortant vaccine. Immunocompromised contacts should be advised to avoid contact with stool from the immunised child if possible, particularly after the first vaccine dose for at least 14 days. Since the risk of vaccine transmission and subsequent vaccine-derived disease with the current vaccines is much less than the risk of wildtype rotavirus disease in immunocompromised contacts, vaccination should be encouraged.</description><identifier>ISSN: 1473-3099</identifier><identifier>EISSN: 1474-4457</identifier><identifier>DOI: 10.1016/S1473-3099(08)70231-7</identifier><identifier>PMID: 18922486</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>London: Elsevier Ltd</publisher><subject>Biological and medical sciences ; Disease transmission ; Gastroenteritis ; Herd immunity ; Human viral diseases ; Humans ; Immunization ; Infectious Disease ; Infectious diseases ; Medical sciences ; Risk Factors ; Rotavirus - physiology ; Rotavirus Infections - immunology ; Rotavirus Infections - prevention &amp; control ; Rotavirus Infections - transmission ; Rotavirus Infections - virology ; Rotavirus Vaccines - adverse effects ; Vaccines ; Viral diseases ; Viral diseases of the digestive system ; Virus Shedding - physiology</subject><ispartof>The Lancet infectious diseases, 2008-10, Vol.8 (10), p.642-649</ispartof><rights>Elsevier Ltd</rights><rights>2008 Elsevier Ltd</rights><rights>2008 INIST-CNRS</rights><rights>Copyright Elsevier Limited Oct 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-5ba2c75f910bbd929036df87a13c74f5d0b740d16c86db28162c9fe105692d2f3</citedby><cites>FETCH-LOGICAL-c475t-5ba2c75f910bbd929036df87a13c74f5d0b740d16c86db28162c9fe105692d2f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/201564474?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994,64384,64386,64388,72240</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20655966$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18922486$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Anderson, Evan J, Dr</creatorcontrib><title>Rotavirus vaccines: viral shedding and risk of transmission</title><title>The Lancet infectious diseases</title><addtitle>Lancet Infect Dis</addtitle><description>Summary Rotavirus causes gastroenteritis in almost all children by 5 years of age. Immunity to rotavirus is incomplete, with potential for recurrent infections occurring throughout life. Live rotavirus vaccines have been developed for the protection of children from severe wildtype rotavirus infections. Transmission of vaccine virus strains from vaccinated children to unvaccinated contacts harbours the potential for herd immunity, but also the risk of vaccine-derived disease in immunocompromised contacts. A review of rotavirus vaccine prelicensure studies shows that viral shedding and transmission were higher with the old tetravalent rhesus rotavirus vaccine than with the current human attenuated monovalent rotavirus vaccine and the pentavalent bovine-human reassortant vaccine. Immunocompromised contacts should be advised to avoid contact with stool from the immunised child if possible, particularly after the first vaccine dose for at least 14 days. Since the risk of vaccine transmission and subsequent vaccine-derived disease with the current vaccines is much less than the risk of wildtype rotavirus disease in immunocompromised contacts, vaccination should be encouraged.</description><subject>Biological and medical sciences</subject><subject>Disease transmission</subject><subject>Gastroenteritis</subject><subject>Herd immunity</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunization</subject><subject>Infectious Disease</subject><subject>Infectious diseases</subject><subject>Medical sciences</subject><subject>Risk Factors</subject><subject>Rotavirus - physiology</subject><subject>Rotavirus Infections - immunology</subject><subject>Rotavirus Infections - prevention &amp; control</subject><subject>Rotavirus Infections - transmission</subject><subject>Rotavirus Infections - virology</subject><subject>Rotavirus Vaccines - adverse effects</subject><subject>Vaccines</subject><subject>Viral diseases</subject><subject>Viral diseases of the digestive system</subject><subject>Virus Shedding - physiology</subject><issn>1473-3099</issn><issn>1474-4457</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqFkFtrFTEURgdRbK3-BGUQFH0Y3cnkqqBI8QYFwctzyOSiaedk2uyZA_335pw5VOiLT7mw9pcvq2keE3hFgIjXPwiTfdeD1i9AvZRAe9LJO81xvWYdY1ze3e9X5Kh5gHgOQCQBdr85IkpTypQ4bt5-n2a7TWXBdmudSzngm7ae7djin-B9yr9bm31bEl60U2znYjNuEmKa8sPmXrQjhkeH9aT59enjz9Mv3dm3z19PP5x1jkk-d3yw1EkeNYFh8Jpq6IWPSlrSO8ki9zBIBp4Ip4QfqCKCOh0DAS409TT2J83zNfeyTFdLwNnUAi6Mo81hWtAILaSiDCr49BZ4Pi0l126GAuGCVTcV4ivkyoRYQjSXJW1suTYEzE6t2as1O28GlNmrNbLOPTmEL8Mm-H9TB5cVeHYALDo7xmrKJbzhKAjOtdhx71cuVGfbFIpBl0J2wacS3Gz8lP5b5d2tBDemnOqjF-E64M2niUFqYA3ZZYDaJ8j-Ly4tqLo</recordid><startdate>20081001</startdate><enddate>20081001</enddate><creator>Anderson, Evan J, Dr</creator><general>Elsevier Ltd</general><general>Lancet Publishing Group</general><general>Elsevier Limited</general><scope>IQODW</scope><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>0TZ</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20081001</creationdate><title>Rotavirus vaccines: viral shedding and risk of transmission</title><author>Anderson, Evan J, Dr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-5ba2c75f910bbd929036df87a13c74f5d0b740d16c86db28162c9fe105692d2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Biological and medical sciences</topic><topic>Disease transmission</topic><topic>Gastroenteritis</topic><topic>Herd immunity</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunization</topic><topic>Infectious Disease</topic><topic>Infectious diseases</topic><topic>Medical sciences</topic><topic>Risk Factors</topic><topic>Rotavirus - physiology</topic><topic>Rotavirus Infections - immunology</topic><topic>Rotavirus Infections - prevention &amp; control</topic><topic>Rotavirus Infections - transmission</topic><topic>Rotavirus Infections - virology</topic><topic>Rotavirus Vaccines - adverse effects</topic><topic>Vaccines</topic><topic>Viral diseases</topic><topic>Viral diseases of the digestive system</topic><topic>Virus Shedding - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anderson, Evan J, Dr</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Lancet Titles</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>The Lancet infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anderson, Evan J, Dr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rotavirus vaccines: viral shedding and risk of transmission</atitle><jtitle>The Lancet infectious diseases</jtitle><addtitle>Lancet Infect Dis</addtitle><date>2008-10-01</date><risdate>2008</risdate><volume>8</volume><issue>10</issue><spage>642</spage><epage>649</epage><pages>642-649</pages><issn>1473-3099</issn><eissn>1474-4457</eissn><coden>LANCAO</coden><abstract>Summary Rotavirus causes gastroenteritis in almost all children by 5 years of age. Immunity to rotavirus is incomplete, with potential for recurrent infections occurring throughout life. Live rotavirus vaccines have been developed for the protection of children from severe wildtype rotavirus infections. Transmission of vaccine virus strains from vaccinated children to unvaccinated contacts harbours the potential for herd immunity, but also the risk of vaccine-derived disease in immunocompromised contacts. A review of rotavirus vaccine prelicensure studies shows that viral shedding and transmission were higher with the old tetravalent rhesus rotavirus vaccine than with the current human attenuated monovalent rotavirus vaccine and the pentavalent bovine-human reassortant vaccine. Immunocompromised contacts should be advised to avoid contact with stool from the immunised child if possible, particularly after the first vaccine dose for at least 14 days. Since the risk of vaccine transmission and subsequent vaccine-derived disease with the current vaccines is much less than the risk of wildtype rotavirus disease in immunocompromised contacts, vaccination should be encouraged.</abstract><cop>London</cop><pub>Elsevier Ltd</pub><pmid>18922486</pmid><doi>10.1016/S1473-3099(08)70231-7</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1473-3099
ispartof The Lancet infectious diseases, 2008-10, Vol.8 (10), p.642-649
issn 1473-3099
1474-4457
language eng
recordid cdi_proquest_miscellaneous_69678240
source MEDLINE; ScienceDirect Journals (5 years ago - present); ProQuest Central UK/Ireland
subjects Biological and medical sciences
Disease transmission
Gastroenteritis
Herd immunity
Human viral diseases
Humans
Immunization
Infectious Disease
Infectious diseases
Medical sciences
Risk Factors
Rotavirus - physiology
Rotavirus Infections - immunology
Rotavirus Infections - prevention & control
Rotavirus Infections - transmission
Rotavirus Infections - virology
Rotavirus Vaccines - adverse effects
Vaccines
Viral diseases
Viral diseases of the digestive system
Virus Shedding - physiology
title Rotavirus vaccines: viral shedding and risk of transmission
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T12%3A43%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Rotavirus%20vaccines:%20viral%20shedding%20and%20risk%20of%20transmission&rft.jtitle=The%20Lancet%20infectious%20diseases&rft.au=Anderson,%20Evan%20J,%20Dr&rft.date=2008-10-01&rft.volume=8&rft.issue=10&rft.spage=642&rft.epage=649&rft.pages=642-649&rft.issn=1473-3099&rft.eissn=1474-4457&rft.coden=LANCAO&rft_id=info:doi/10.1016/S1473-3099(08)70231-7&rft_dat=%3Cproquest_cross%3E69678240%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=201564474&rft_id=info:pmid/18922486&rft_els_id=S1473309908702317&rfr_iscdi=true