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Persistence of Antibodies to 2 Virus-Like Particle Norovirus Vaccine Candidate Formulations in Healthy Adults: 1-Year Follow-up With Memory Probe Vaccination
We previously reported the tolerability and immunogenicity 1 month after intramuscular administration of 2 bivalent virus-like particle (VLP)-based candidate norovirus vaccine formulations in adults. We now describe the persistence of immunity and responses to a memory probe vaccination 1 year later...
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Published in: | The Journal of infectious diseases 2019-07, Vol.220 (4), p.603-614 |
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creator | Atmar, Robert L Baehner, Frank Cramer, Jakob P Lloyd, Eric Sherwood, James Borkowski, Astrid Mendelman, Paul M |
description | We previously reported the tolerability and immunogenicity 1 month after intramuscular administration of 2 bivalent virus-like particle (VLP)-based candidate norovirus vaccine formulations in adults. We now describe the persistence of immunity and responses to a memory probe vaccination 1 year later.
A total of 454 healthy men and women aged 18-49 years in 3 equal groups received placebo (saline) or 15/50 or 50/50 vaccine formulations (ie, 15 or 50 µg of GI.1 genotype VLPs, respectively, and 50 µg of GII.4c VLPs) with MPL and Al(OH)3. Immunogenicity and safety were assessed up to day 365, when 351 participants received a memory probe vaccination of 15 µg each of GI.1 and GII.4c VLPs with Al(OH)3.
No safety signals were detected up to 1 year after the first vaccination. Pan-immunoglobulin, immunoglobulin A, and histo-blood group antigen-blocking (HBGA) antibody levels among vaccinees waned but remained higher than levels before vaccination and levels in placebo recipients on days 180 and 365. Memory probe vaccination increased all antibody titers. Levels of HBGA antibodies to GI.1 but not GII.4c were higher after the first vaccination in candidate vaccine groups, compared with those in the placebo group.
Levels of antibodies to both candidate norovirus VLP formulations persisted above baseline levels for at least 1 year after primary vaccination. HBGA-blocking responses to the memory probe for GI.1 but not GII.4c displayed characteristics of immune memory.
NCT02142504. |
doi_str_mv | 10.1093/infdis/jiz170 |
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A total of 454 healthy men and women aged 18-49 years in 3 equal groups received placebo (saline) or 15/50 or 50/50 vaccine formulations (ie, 15 or 50 µg of GI.1 genotype VLPs, respectively, and 50 µg of GII.4c VLPs) with MPL and Al(OH)3. Immunogenicity and safety were assessed up to day 365, when 351 participants received a memory probe vaccination of 15 µg each of GI.1 and GII.4c VLPs with Al(OH)3.
No safety signals were detected up to 1 year after the first vaccination. Pan-immunoglobulin, immunoglobulin A, and histo-blood group antigen-blocking (HBGA) antibody levels among vaccinees waned but remained higher than levels before vaccination and levels in placebo recipients on days 180 and 365. Memory probe vaccination increased all antibody titers. Levels of HBGA antibodies to GI.1 but not GII.4c were higher after the first vaccination in candidate vaccine groups, compared with those in the placebo group.
Levels of antibodies to both candidate norovirus VLP formulations persisted above baseline levels for at least 1 year after primary vaccination. HBGA-blocking responses to the memory probe for GI.1 but not GII.4c displayed characteristics of immune memory.
NCT02142504.</description><identifier>ISSN: 0022-1899</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiz170</identifier><identifier>PMID: 31001633</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Antibodies ; Clinical trials ; Genotypes ; Immunogenicity ; Immunoglobulin A ; Immunoglobulins ; Immunological memory ; Vaccination ; Vaccines ; Virus-like particles</subject><ispartof>The Journal of infectious diseases, 2019-07, Vol.220 (4), p.603-614</ispartof><rights>The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c251t-ea16e3d2bb7029634edb098f08be196cc8f49d1e83675a05abc4a9bafce885dc3</citedby><cites>FETCH-LOGICAL-c251t-ea16e3d2bb7029634edb098f08be196cc8f49d1e83675a05abc4a9bafce885dc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31001633$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Atmar, Robert L</creatorcontrib><creatorcontrib>Baehner, Frank</creatorcontrib><creatorcontrib>Cramer, Jakob P</creatorcontrib><creatorcontrib>Lloyd, Eric</creatorcontrib><creatorcontrib>Sherwood, James</creatorcontrib><creatorcontrib>Borkowski, Astrid</creatorcontrib><creatorcontrib>Mendelman, Paul M</creatorcontrib><creatorcontrib>NOR-201 Study Group</creatorcontrib><creatorcontrib>NOR-201 Study Group</creatorcontrib><title>Persistence of Antibodies to 2 Virus-Like Particle Norovirus Vaccine Candidate Formulations in Healthy Adults: 1-Year Follow-up With Memory Probe Vaccination</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>We previously reported the tolerability and immunogenicity 1 month after intramuscular administration of 2 bivalent virus-like particle (VLP)-based candidate norovirus vaccine formulations in adults. We now describe the persistence of immunity and responses to a memory probe vaccination 1 year later.
A total of 454 healthy men and women aged 18-49 years in 3 equal groups received placebo (saline) or 15/50 or 50/50 vaccine formulations (ie, 15 or 50 µg of GI.1 genotype VLPs, respectively, and 50 µg of GII.4c VLPs) with MPL and Al(OH)3. Immunogenicity and safety were assessed up to day 365, when 351 participants received a memory probe vaccination of 15 µg each of GI.1 and GII.4c VLPs with Al(OH)3.
No safety signals were detected up to 1 year after the first vaccination. Pan-immunoglobulin, immunoglobulin A, and histo-blood group antigen-blocking (HBGA) antibody levels among vaccinees waned but remained higher than levels before vaccination and levels in placebo recipients on days 180 and 365. Memory probe vaccination increased all antibody titers. Levels of HBGA antibodies to GI.1 but not GII.4c were higher after the first vaccination in candidate vaccine groups, compared with those in the placebo group.
Levels of antibodies to both candidate norovirus VLP formulations persisted above baseline levels for at least 1 year after primary vaccination. HBGA-blocking responses to the memory probe for GI.1 but not GII.4c displayed characteristics of immune memory.
NCT02142504.</description><subject>Antibodies</subject><subject>Clinical trials</subject><subject>Genotypes</subject><subject>Immunogenicity</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulins</subject><subject>Immunological memory</subject><subject>Vaccination</subject><subject>Vaccines</subject><subject>Virus-like particles</subject><issn>0022-1899</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpdkctuEzEUQC0EomlhyRZZYtONqR_zMrsoohQphSygiNXIjzuqg8cOtqco_Ev_lWkTWLC60tXR0b06CL1i9C2jUly4MFiXL7buN2vpE7RgtWhJ0zDxFC0o5ZywTsoTdJrzllJaiaZ9jk4Eo5Q1QizQ_QZSdrlAMIDjgJehOB2tg4xLxBzfuDRlsnY_AG9UKs54wJ9iincPe3yjjHEB8EoF66wqgC9jGievioshYxfwFShfbvd4aSdf8jvMyHdQaca8j7_ItMPfXLnF1zDGtMebFDUcpY-KF-jZoHyGl8d5hr5evv-yuiLrzx8-rpZrYnjNCgHFGhCWa91SLhtRgdVUdgPtNDDZGNMNlbQMuvn7WtFaaVMpqdVgoOtqa8QZOj94dyn-nCCXfnTZgPcqQJxyzzljsmqlaGb0zX_oNk4pzNf1vKo63taUtTNFDpRJMecEQ79LblRp3zPaP3TrD936Q7eZf320TnoE-4_-G0r8ARwxl7k</recordid><startdate>20190719</startdate><enddate>20190719</enddate><creator>Atmar, Robert L</creator><creator>Baehner, Frank</creator><creator>Cramer, Jakob P</creator><creator>Lloyd, Eric</creator><creator>Sherwood, James</creator><creator>Borkowski, Astrid</creator><creator>Mendelman, Paul M</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20190719</creationdate><title>Persistence of Antibodies to 2 Virus-Like Particle Norovirus Vaccine Candidate Formulations in Healthy Adults: 1-Year Follow-up With Memory Probe Vaccination</title><author>Atmar, Robert L ; Baehner, Frank ; Cramer, Jakob P ; Lloyd, Eric ; Sherwood, James ; Borkowski, Astrid ; Mendelman, Paul M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c251t-ea16e3d2bb7029634edb098f08be196cc8f49d1e83675a05abc4a9bafce885dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Antibodies</topic><topic>Clinical trials</topic><topic>Genotypes</topic><topic>Immunogenicity</topic><topic>Immunoglobulin A</topic><topic>Immunoglobulins</topic><topic>Immunological memory</topic><topic>Vaccination</topic><topic>Vaccines</topic><topic>Virus-like particles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Atmar, Robert L</creatorcontrib><creatorcontrib>Baehner, Frank</creatorcontrib><creatorcontrib>Cramer, Jakob P</creatorcontrib><creatorcontrib>Lloyd, Eric</creatorcontrib><creatorcontrib>Sherwood, James</creatorcontrib><creatorcontrib>Borkowski, Astrid</creatorcontrib><creatorcontrib>Mendelman, Paul M</creatorcontrib><creatorcontrib>NOR-201 Study Group</creatorcontrib><creatorcontrib>NOR-201 Study Group</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Atmar, Robert L</au><au>Baehner, Frank</au><au>Cramer, Jakob P</au><au>Lloyd, Eric</au><au>Sherwood, James</au><au>Borkowski, Astrid</au><au>Mendelman, Paul M</au><aucorp>NOR-201 Study Group</aucorp><aucorp>NOR-201 Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Persistence of Antibodies to 2 Virus-Like Particle Norovirus Vaccine Candidate Formulations in Healthy Adults: 1-Year Follow-up With Memory Probe Vaccination</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2019-07-19</date><risdate>2019</risdate><volume>220</volume><issue>4</issue><spage>603</spage><epage>614</epage><pages>603-614</pages><issn>0022-1899</issn><eissn>1537-6613</eissn><abstract>We previously reported the tolerability and immunogenicity 1 month after intramuscular administration of 2 bivalent virus-like particle (VLP)-based candidate norovirus vaccine formulations in adults. We now describe the persistence of immunity and responses to a memory probe vaccination 1 year later.
A total of 454 healthy men and women aged 18-49 years in 3 equal groups received placebo (saline) or 15/50 or 50/50 vaccine formulations (ie, 15 or 50 µg of GI.1 genotype VLPs, respectively, and 50 µg of GII.4c VLPs) with MPL and Al(OH)3. Immunogenicity and safety were assessed up to day 365, when 351 participants received a memory probe vaccination of 15 µg each of GI.1 and GII.4c VLPs with Al(OH)3.
No safety signals were detected up to 1 year after the first vaccination. Pan-immunoglobulin, immunoglobulin A, and histo-blood group antigen-blocking (HBGA) antibody levels among vaccinees waned but remained higher than levels before vaccination and levels in placebo recipients on days 180 and 365. Memory probe vaccination increased all antibody titers. Levels of HBGA antibodies to GI.1 but not GII.4c were higher after the first vaccination in candidate vaccine groups, compared with those in the placebo group.
Levels of antibodies to both candidate norovirus VLP formulations persisted above baseline levels for at least 1 year after primary vaccination. HBGA-blocking responses to the memory probe for GI.1 but not GII.4c displayed characteristics of immune memory.
NCT02142504.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>31001633</pmid><doi>10.1093/infdis/jiz170</doi><tpages>12</tpages></addata></record> |
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subjects | Antibodies Clinical trials Genotypes Immunogenicity Immunoglobulin A Immunoglobulins Immunological memory Vaccination Vaccines Virus-like particles |
title | Persistence of Antibodies to 2 Virus-Like Particle Norovirus Vaccine Candidate Formulations in Healthy Adults: 1-Year Follow-up With Memory Probe Vaccination |
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