AS03-adjuvanted H5N1 vaccine promotes antibody diversity and affinity maturation, NAI titers, cross-clade H5N1 neutralization, but not H1N1 cross-subtype neutralization
Immune responses to inactivated vaccines against avian influenza are poor due in part to lack of immune memory. Adjuvants significantly increased virus neutralizing titers. We performed comprehensive analyses of polyclonal antibody responses following FDA-approved adjuvanted H5N1-A/Indonesia vaccine...
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description | Immune responses to inactivated vaccines against avian influenza are poor due in part to lack of immune memory. Adjuvants significantly increased virus neutralizing titers. We performed comprehensive analyses of polyclonal antibody responses following FDA-approved adjuvanted H5N1-A/Indonesia vaccine, administered in presence or absence of AS03. Using Whole Genome Fragment Phage Display Libraries, we observed that AS03 induced antibody epitope diversity to viral hemagglutinin (HA) and neuraminidase compared with unadjuvanted vaccine. Furthermore, AS03 promoted significant antibody affinity maturation to properly folded H5-HA1 (but not to HA2) domain, which correlated with neutralization titers against both vaccine and heterologous H5N1 strains. However, no increase in heterosubtypic cross-neutralization of Group1-H1N1 seasonal strains was observed. AS03-H5N1 vaccine also induced higher neuraminidase inhibition antibody titers. This study provides insight into the differential impacts of AS03 adjuvant on H5N1 vaccine-induced antibody responses that may help optimize vaccine platforms for future vaccines with improved protection against seasonal and pandemic influenza strains.
Influenza: understanding the mechanisms of vaccine-boosting additives
Adjuvant AS03 improves a bird flu vaccine’s ability to recognize and bind to virion targets. Avian influenza viruses are considered a pandemic threat, and vaccines made from inactivated virus are limited in their efficacy. However, adjuvants such as AS03 have the ability to augment a host’s immunity, prompting Surender Khurana and colleagues from the United States’ Food and Drug Administration to investigate how. In an H5N1 vaccine trial, researchers found that AS03 improved immune responses by increasing the degree, diversity, and intensity of antibody binding to viral surface proteins, which likely caused the observed increase in the neutralization of the virus tested as well as efficacy against other H5N1 strains. The AS03-adjuvanted vaccine did not neutralize seasonal H1N1 influenza strains. This study may inform future vaccine development efforts by partially illuminating the effects of AS03. |
doi_str_mv | 10.1038/s41541-018-0076-2 |
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Influenza: understanding the mechanisms of vaccine-boosting additives
Adjuvant AS03 improves a bird flu vaccine’s ability to recognize and bind to virion targets. Avian influenza viruses are considered a pandemic threat, and vaccines made from inactivated virus are limited in their efficacy. However, adjuvants such as AS03 have the ability to augment a host’s immunity, prompting Surender Khurana and colleagues from the United States’ Food and Drug Administration to investigate how. In an H5N1 vaccine trial, researchers found that AS03 improved immune responses by increasing the degree, diversity, and intensity of antibody binding to viral surface proteins, which likely caused the observed increase in the neutralization of the virus tested as well as efficacy against other H5N1 strains. The AS03-adjuvanted vaccine did not neutralize seasonal H1N1 influenza strains. This study may inform future vaccine development efforts by partially illuminating the effects of AS03.</description><identifier>ISSN: 2059-0105</identifier><identifier>EISSN: 2059-0105</identifier><identifier>DOI: 10.1038/s41541-018-0076-2</identifier><identifier>PMID: 30302282</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/250/590/2291 ; 631/326/590/2291 ; Adjuvants ; Avian flu ; Biomedical and Life Sciences ; Biomedicine ; Infectious Diseases ; Medical Microbiology ; Pandemics ; Public Health ; Swine flu ; Vaccine ; Vaccines ; Virology ; Viruses</subject><ispartof>npj vaccines, 2018-10, Vol.3 (1), p.40-40, Article 40</ispartof><rights>The Author(s) 2018</rights><rights>The Author(s) 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (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-c470t-e293eb0d2a0d6c54b82f6f46cbfc59a5523bfcaf9364d95d23be10092f5e789a3</citedby><cites>FETCH-LOGICAL-c470t-e293eb0d2a0d6c54b82f6f46cbfc59a5523bfcaf9364d95d23be10092f5e789a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167326/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167326/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30302282$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khurana, Surender</creatorcontrib><creatorcontrib>Coyle, Elizabeth M.</creatorcontrib><creatorcontrib>Manischewitz, Jody</creatorcontrib><creatorcontrib>King, Lisa R.</creatorcontrib><creatorcontrib>Gao, Jin</creatorcontrib><creatorcontrib>Germain, Ronald N.</creatorcontrib><creatorcontrib>Schwartzberg, Pamela L.</creatorcontrib><creatorcontrib>Tsang, John S.</creatorcontrib><creatorcontrib>Golding, Hana</creatorcontrib><creatorcontrib>and the CHI Consortium</creatorcontrib><creatorcontrib>and the CHI Consortium</creatorcontrib><title>AS03-adjuvanted H5N1 vaccine promotes antibody diversity and affinity maturation, NAI titers, cross-clade H5N1 neutralization, but not H1N1 cross-subtype neutralization</title><title>npj vaccines</title><addtitle>npj Vaccines</addtitle><addtitle>NPJ Vaccines</addtitle><description>Immune responses to inactivated vaccines against avian influenza are poor due in part to lack of immune memory. Adjuvants significantly increased virus neutralizing titers. We performed comprehensive analyses of polyclonal antibody responses following FDA-approved adjuvanted H5N1-A/Indonesia vaccine, administered in presence or absence of AS03. Using Whole Genome Fragment Phage Display Libraries, we observed that AS03 induced antibody epitope diversity to viral hemagglutinin (HA) and neuraminidase compared with unadjuvanted vaccine. Furthermore, AS03 promoted significant antibody affinity maturation to properly folded H5-HA1 (but not to HA2) domain, which correlated with neutralization titers against both vaccine and heterologous H5N1 strains. However, no increase in heterosubtypic cross-neutralization of Group1-H1N1 seasonal strains was observed. AS03-H5N1 vaccine also induced higher neuraminidase inhibition antibody titers. This study provides insight into the differential impacts of AS03 adjuvant on H5N1 vaccine-induced antibody responses that may help optimize vaccine platforms for future vaccines with improved protection against seasonal and pandemic influenza strains.
Influenza: understanding the mechanisms of vaccine-boosting additives
Adjuvant AS03 improves a bird flu vaccine’s ability to recognize and bind to virion targets. Avian influenza viruses are considered a pandemic threat, and vaccines made from inactivated virus are limited in their efficacy. However, adjuvants such as AS03 have the ability to augment a host’s immunity, prompting Surender Khurana and colleagues from the United States’ Food and Drug Administration to investigate how. In an H5N1 vaccine trial, researchers found that AS03 improved immune responses by increasing the degree, diversity, and intensity of antibody binding to viral surface proteins, which likely caused the observed increase in the neutralization of the virus tested as well as efficacy against other H5N1 strains. The AS03-adjuvanted vaccine did not neutralize seasonal H1N1 influenza strains. This study may inform future vaccine development efforts by partially illuminating the effects of AS03.</description><subject>631/250/590/2291</subject><subject>631/326/590/2291</subject><subject>Adjuvants</subject><subject>Avian flu</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Infectious Diseases</subject><subject>Medical Microbiology</subject><subject>Pandemics</subject><subject>Public Health</subject><subject>Swine flu</subject><subject>Vaccine</subject><subject>Vaccines</subject><subject>Virology</subject><subject>Viruses</subject><issn>2059-0105</issn><issn>2059-0105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp1ks9vFCEUxydGY5u1f4AXQ-LFQ0cfMDDDxWTTWLdJUw_qmTDAVDazsAKzyfYv8s8s66y1NvHE-_F5X96DV1WvMbzHQLsPqcGswTXgrgZoeU2eVacEmCgRYM8f2SfVWUprAMAtp6yFl9UJBQqEdOS0-rX8CrRWZj3tlM_WoBW7wWintHbeom0Mm5BtQiXn-mD2yLidjcnlfQkZpIbB-YOzUXmKKrvgz9HN8gpllwt2jnQMKdV6VMbOyt5OOarR3R3hfsrIh4xWuCRnOk193m_tE_RV9WJQY7Jnx3NRfb_89O1iVV9_-Xx1sbyuddNCri0R1PZgiALDNWv6jgx8aLjuB82EYozQYqlBUN4YwUxxLQYQZGC27YSii-rjrLud-o012vpDE3Ib3UbFvQzKyX8z3v2Qt2EnOeYtJbwIvDsKxPBzsinLjUvajqPyNkxJEozbjoAQTUHfPkHXYYq-jCcJ7QTnHQhWKDxTv58n2uGhGQzysApyXgVZVkEeVqEUL6o3j6d4qPjz8QUgM5BKyt_a-Pfq_6veA2FowWE</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Khurana, Surender</creator><creator>Coyle, Elizabeth M.</creator><creator>Manischewitz, Jody</creator><creator>King, Lisa R.</creator><creator>Gao, Jin</creator><creator>Germain, Ronald N.</creator><creator>Schwartzberg, Pamela L.</creator><creator>Tsang, John S.</creator><creator>Golding, Hana</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88C</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M0T</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20181001</creationdate><title>AS03-adjuvanted H5N1 vaccine promotes antibody diversity and affinity maturation, NAI titers, cross-clade H5N1 neutralization, but not H1N1 cross-subtype neutralization</title><author>Khurana, Surender ; Coyle, Elizabeth M. ; Manischewitz, Jody ; King, Lisa R. ; Gao, Jin ; Germain, Ronald N. ; Schwartzberg, Pamela L. ; Tsang, John S. ; Golding, Hana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-e293eb0d2a0d6c54b82f6f46cbfc59a5523bfcaf9364d95d23be10092f5e789a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>631/250/590/2291</topic><topic>631/326/590/2291</topic><topic>Adjuvants</topic><topic>Avian flu</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Infectious Diseases</topic><topic>Medical Microbiology</topic><topic>Pandemics</topic><topic>Public Health</topic><topic>Swine flu</topic><topic>Vaccine</topic><topic>Vaccines</topic><topic>Virology</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khurana, Surender</creatorcontrib><creatorcontrib>Coyle, Elizabeth M.</creatorcontrib><creatorcontrib>Manischewitz, Jody</creatorcontrib><creatorcontrib>King, Lisa R.</creatorcontrib><creatorcontrib>Gao, Jin</creatorcontrib><creatorcontrib>Germain, Ronald N.</creatorcontrib><creatorcontrib>Schwartzberg, Pamela L.</creatorcontrib><creatorcontrib>Tsang, John S.</creatorcontrib><creatorcontrib>Golding, Hana</creatorcontrib><creatorcontrib>and the CHI Consortium</creatorcontrib><creatorcontrib>and the CHI Consortium</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Public Health Database</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 Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</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>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Nursing & Allied Health Premium</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><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>npj vaccines</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khurana, Surender</au><au>Coyle, Elizabeth M.</au><au>Manischewitz, Jody</au><au>King, Lisa R.</au><au>Gao, Jin</au><au>Germain, Ronald N.</au><au>Schwartzberg, Pamela L.</au><au>Tsang, John S.</au><au>Golding, Hana</au><aucorp>and the CHI Consortium</aucorp><aucorp>and the CHI Consortium</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>AS03-adjuvanted H5N1 vaccine promotes antibody diversity and affinity maturation, NAI titers, cross-clade H5N1 neutralization, but not H1N1 cross-subtype neutralization</atitle><jtitle>npj vaccines</jtitle><stitle>npj Vaccines</stitle><addtitle>NPJ Vaccines</addtitle><date>2018-10-01</date><risdate>2018</risdate><volume>3</volume><issue>1</issue><spage>40</spage><epage>40</epage><pages>40-40</pages><artnum>40</artnum><issn>2059-0105</issn><eissn>2059-0105</eissn><abstract>Immune responses to inactivated vaccines against avian influenza are poor due in part to lack of immune memory. Adjuvants significantly increased virus neutralizing titers. We performed comprehensive analyses of polyclonal antibody responses following FDA-approved adjuvanted H5N1-A/Indonesia vaccine, administered in presence or absence of AS03. Using Whole Genome Fragment Phage Display Libraries, we observed that AS03 induced antibody epitope diversity to viral hemagglutinin (HA) and neuraminidase compared with unadjuvanted vaccine. Furthermore, AS03 promoted significant antibody affinity maturation to properly folded H5-HA1 (but not to HA2) domain, which correlated with neutralization titers against both vaccine and heterologous H5N1 strains. However, no increase in heterosubtypic cross-neutralization of Group1-H1N1 seasonal strains was observed. AS03-H5N1 vaccine also induced higher neuraminidase inhibition antibody titers. This study provides insight into the differential impacts of AS03 adjuvant on H5N1 vaccine-induced antibody responses that may help optimize vaccine platforms for future vaccines with improved protection against seasonal and pandemic influenza strains.
Influenza: understanding the mechanisms of vaccine-boosting additives
Adjuvant AS03 improves a bird flu vaccine’s ability to recognize and bind to virion targets. Avian influenza viruses are considered a pandemic threat, and vaccines made from inactivated virus are limited in their efficacy. However, adjuvants such as AS03 have the ability to augment a host’s immunity, prompting Surender Khurana and colleagues from the United States’ Food and Drug Administration to investigate how. In an H5N1 vaccine trial, researchers found that AS03 improved immune responses by increasing the degree, diversity, and intensity of antibody binding to viral surface proteins, which likely caused the observed increase in the neutralization of the virus tested as well as efficacy against other H5N1 strains. The AS03-adjuvanted vaccine did not neutralize seasonal H1N1 influenza strains. This study may inform future vaccine development efforts by partially illuminating the effects of AS03.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>30302282</pmid><doi>10.1038/s41541-018-0076-2</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/250/590/2291 631/326/590/2291 Adjuvants Avian flu Biomedical and Life Sciences Biomedicine Infectious Diseases Medical Microbiology Pandemics Public Health Swine flu Vaccine Vaccines Virology Viruses |
title | AS03-adjuvanted H5N1 vaccine promotes antibody diversity and affinity maturation, NAI titers, cross-clade H5N1 neutralization, but not H1N1 cross-subtype neutralization |
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