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HIV virological suppression influences response to the AS 03‐adjuvanted monovalent pandemic influenza A H 1 N 1 vaccine in HIV ‐infected children
DesignChildren with HIV are especially susceptible to complications from influenza infection, and effective vaccines are central to reducing disease burden in this population. We undertook a prospective, observational study to investigate the safety and immunogenicity of the inactivated split‐virion...
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Published in: | Influenza and other respiratory viruses 2014-05, Vol.8 (3), p.360-366 |
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description | DesignChildren with HIV are especially susceptible to complications from influenza infection, and effective vaccines are central to reducing disease burden in this population. We undertook a prospective, observational study to investigate the safety and immunogenicity of the inactivated split‐virion AS03‐adjuvanted pandemic H1N1(2009) vaccine in children with HIV.SettingNational referral centre for Paediatric HIV in Ireland.SampleTwenty four children with HIV were recruited consecutively and received two doses of the vaccine. The serological response was measured before each vaccine dose (Day 0 and Day 28) and 2 months after the booster dose. Antibody titres were measured using a haemagglutination inhibition (HAI) assay. Seroprotection was defined as a HAI titre ≥ 1:40; seroconversion was defined as a ≥ fourfold increase in antibody titre and a postvaccination titre ≥ 1:40.Main outcome measuresThe seroconversion rates after prime and booster doses were 75% and 71%, respectively. HIV virological suppression at the time of immunization was associated with a significantly increased seroconversion rate (P = 0·009), magnitude of serological response (P = 0·02) and presence of seroprotective HAI titres (P = 0·017) two months after the booster dose. No other factor was significantly associated with the seroconversion/seroprotection rate. No serious adverse effects were reported. Vaccination had no impact on HIV disease progression. The AS03‐adjuvanted pandemic H1N1 vaccine appears to be safe and immunogenic among HIV‐infected children. A robust serological response appears to be optimized by adherence to a HAART regimen delivering virological suppression. |
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We undertook a prospective, observational study to investigate the safety and immunogenicity of the inactivated split‐virion AS03‐adjuvanted pandemic H1N1(2009) vaccine in children with HIV.SettingNational referral centre for Paediatric HIV in Ireland.SampleTwenty four children with HIV were recruited consecutively and received two doses of the vaccine. The serological response was measured before each vaccine dose (Day 0 and Day 28) and 2 months after the booster dose. Antibody titres were measured using a haemagglutination inhibition (HAI) assay. Seroprotection was defined as a HAI titre ≥ 1:40; seroconversion was defined as a ≥ fourfold increase in antibody titre and a postvaccination titre ≥ 1:40.Main outcome measuresThe seroconversion rates after prime and booster doses were 75% and 71%, respectively. HIV virological suppression at the time of immunization was associated with a significantly increased seroconversion rate (P = 0·009), magnitude of serological response (P = 0·02) and presence of seroprotective HAI titres (P = 0·017) two months after the booster dose. No other factor was significantly associated with the seroconversion/seroprotection rate. No serious adverse effects were reported. Vaccination had no impact on HIV disease progression. The AS03‐adjuvanted pandemic H1N1 vaccine appears to be safe and immunogenic among HIV‐infected children. A robust serological response appears to be optimized by adherence to a HAART regimen delivering virological suppression.</description><identifier>ISSN: 1750-2640</identifier><identifier>EISSN: 1750-2659</identifier><identifier>DOI: 10.1111/irv.12243</identifier><language>eng</language><publisher>Chichester: John Wiley & Sons, Inc</publisher><subject>Antibodies ; Children ; Complications ; Dosage ; Hemagglutination inhibition ; Highly active antiretroviral therapy ; HIV ; Human immunodeficiency virus ; Immunization ; Immunogenicity ; Influenza ; Influenza A ; Laboratories ; Pandemics ; Respiratory diseases ; Seroconversion ; Vaccines ; Virions ; Viruses</subject><ispartof>Influenza and other respiratory viruses, 2014-05, Vol.8 (3), p.360-366</ispartof><rights>2014. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1026-1d360f592b70703ed9e4fd75197af31039827c28336ad4a5086fdd9418c891363</citedby><cites>FETCH-LOGICAL-c1026-1d360f592b70703ed9e4fd75197af31039827c28336ad4a5086fdd9418c891363</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2289571456/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2289571456?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25732,27903,27904,36991,44569,74873</link.rule.ids></links><search><creatorcontrib>Leahy, Timothy R.</creatorcontrib><creatorcontrib>Goode, Michelle</creatorcontrib><creatorcontrib>Lynam, Paul</creatorcontrib><creatorcontrib>Gavin, Patrick J.</creatorcontrib><creatorcontrib>Butler, Karina M.</creatorcontrib><title>HIV virological suppression influences response to the AS 03‐adjuvanted monovalent pandemic influenza A H 1 N 1 vaccine in HIV ‐infected children</title><title>Influenza and other respiratory viruses</title><description>DesignChildren with HIV are especially susceptible to complications from influenza infection, and effective vaccines are central to reducing disease burden in this population. We undertook a prospective, observational study to investigate the safety and immunogenicity of the inactivated split‐virion AS03‐adjuvanted pandemic H1N1(2009) vaccine in children with HIV.SettingNational referral centre for Paediatric HIV in Ireland.SampleTwenty four children with HIV were recruited consecutively and received two doses of the vaccine. The serological response was measured before each vaccine dose (Day 0 and Day 28) and 2 months after the booster dose. Antibody titres were measured using a haemagglutination inhibition (HAI) assay. Seroprotection was defined as a HAI titre ≥ 1:40; seroconversion was defined as a ≥ fourfold increase in antibody titre and a postvaccination titre ≥ 1:40.Main outcome measuresThe seroconversion rates after prime and booster doses were 75% and 71%, respectively. HIV virological suppression at the time of immunization was associated with a significantly increased seroconversion rate (P = 0·009), magnitude of serological response (P = 0·02) and presence of seroprotective HAI titres (P = 0·017) two months after the booster dose. No other factor was significantly associated with the seroconversion/seroprotection rate. No serious adverse effects were reported. Vaccination had no impact on HIV disease progression. The AS03‐adjuvanted pandemic H1N1 vaccine appears to be safe and immunogenic among HIV‐infected children. A robust serological response appears to be optimized by adherence to a HAART regimen delivering virological suppression.</description><subject>Antibodies</subject><subject>Children</subject><subject>Complications</subject><subject>Dosage</subject><subject>Hemagglutination inhibition</subject><subject>Highly active antiretroviral therapy</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Immunization</subject><subject>Immunogenicity</subject><subject>Influenza</subject><subject>Influenza A</subject><subject>Laboratories</subject><subject>Pandemics</subject><subject>Respiratory diseases</subject><subject>Seroconversion</subject><subject>Vaccines</subject><subject>Virions</subject><subject>Viruses</subject><issn>1750-2640</issn><issn>1750-2659</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNo9kMtKAzEUhoMoWKsL3yDgykVrLpO5LEtRWyi68LIdYnLGpkyTMZkZ0JWP4MYX9EnMWPXA4RzO-fl--BE6pWRKY10Y308pYwnfQyOaCTJhqSj2__eEHKKjEDaEiDQXyQh9LpaPuDfe1e7ZKFnj0DWNhxCMs9jYqu7AKgg4nhpnA-DW4XYNeHaHCf96_5B60_XStqDx1lnXyxpsixtpNWyN-iO8STzDC0zxTexeKmUsxB8ezCMkqkANCLU2tfZgj9FBJesAJ79zjB6uLu_ni8nq9no5n60mihKWTqjmKalEwZ4ykhEOuoCk0pmgRSYrTgkvcpYplnOeSp1IQfK00rpIaK7ygvKUj9HZjtt499JBaMuN67yNliVjeSEymohBdb5TKe9C8FCVjTdb6V9LSsoh9TKmXv6kzr8BeOh2TA</recordid><startdate>201405</startdate><enddate>201405</enddate><creator>Leahy, Timothy R.</creator><creator>Goode, Michelle</creator><creator>Lynam, Paul</creator><creator>Gavin, Patrick J.</creator><creator>Butler, Karina M.</creator><general>John Wiley & Sons, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T2</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201405</creationdate><title>HIV virological suppression influences response to the AS 03‐adjuvanted monovalent pandemic influenza A H 1 N 1 vaccine in HIV ‐infected children</title><author>Leahy, Timothy R. ; Goode, Michelle ; Lynam, Paul ; Gavin, Patrick J. ; Butler, Karina M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1026-1d360f592b70703ed9e4fd75197af31039827c28336ad4a5086fdd9418c891363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antibodies</topic><topic>Children</topic><topic>Complications</topic><topic>Dosage</topic><topic>Hemagglutination inhibition</topic><topic>Highly active antiretroviral therapy</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Immunization</topic><topic>Immunogenicity</topic><topic>Influenza</topic><topic>Influenza A</topic><topic>Laboratories</topic><topic>Pandemics</topic><topic>Respiratory diseases</topic><topic>Seroconversion</topic><topic>Vaccines</topic><topic>Virions</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leahy, Timothy R.</creatorcontrib><creatorcontrib>Goode, Michelle</creatorcontrib><creatorcontrib>Lynam, Paul</creatorcontrib><creatorcontrib>Gavin, Patrick J.</creatorcontrib><creatorcontrib>Butler, Karina M.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Influenza and other respiratory viruses</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leahy, Timothy R.</au><au>Goode, Michelle</au><au>Lynam, Paul</au><au>Gavin, Patrick J.</au><au>Butler, Karina M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HIV virological suppression influences response to the AS 03‐adjuvanted monovalent pandemic influenza A H 1 N 1 vaccine in HIV ‐infected children</atitle><jtitle>Influenza and other respiratory viruses</jtitle><date>2014-05</date><risdate>2014</risdate><volume>8</volume><issue>3</issue><spage>360</spage><epage>366</epage><pages>360-366</pages><issn>1750-2640</issn><eissn>1750-2659</eissn><abstract>DesignChildren with HIV are especially susceptible to complications from influenza infection, and effective vaccines are central to reducing disease burden in this population. We undertook a prospective, observational study to investigate the safety and immunogenicity of the inactivated split‐virion AS03‐adjuvanted pandemic H1N1(2009) vaccine in children with HIV.SettingNational referral centre for Paediatric HIV in Ireland.SampleTwenty four children with HIV were recruited consecutively and received two doses of the vaccine. The serological response was measured before each vaccine dose (Day 0 and Day 28) and 2 months after the booster dose. Antibody titres were measured using a haemagglutination inhibition (HAI) assay. Seroprotection was defined as a HAI titre ≥ 1:40; seroconversion was defined as a ≥ fourfold increase in antibody titre and a postvaccination titre ≥ 1:40.Main outcome measuresThe seroconversion rates after prime and booster doses were 75% and 71%, respectively. HIV virological suppression at the time of immunization was associated with a significantly increased seroconversion rate (P = 0·009), magnitude of serological response (P = 0·02) and presence of seroprotective HAI titres (P = 0·017) two months after the booster dose. No other factor was significantly associated with the seroconversion/seroprotection rate. No serious adverse effects were reported. Vaccination had no impact on HIV disease progression. The AS03‐adjuvanted pandemic H1N1 vaccine appears to be safe and immunogenic among HIV‐infected children. A robust serological response appears to be optimized by adherence to a HAART regimen delivering virological suppression.</abstract><cop>Chichester</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1111/irv.12243</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Children Complications Dosage Hemagglutination inhibition Highly active antiretroviral therapy HIV Human immunodeficiency virus Immunization Immunogenicity Influenza Influenza A Laboratories Pandemics Respiratory diseases Seroconversion Vaccines Virions Viruses |
title | HIV virological suppression influences response to the AS 03‐adjuvanted monovalent pandemic influenza A H 1 N 1 vaccine in HIV ‐infected children |
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