Response to a hepatitis b polypeptide vaccine in micelle form in a young adult population

Polypeptide micelles with relative molecular weights of 25,000 (p25) and 30,000 (gp30) daltons were prepared from native 22‐nm hepatitis B surface antigen (HBsAg) particles. This p25/gp30 complex was alum‐adsorbed, and three dosage levels (20 m̈g, 4 m̈g, and 0.8 m̈g) were administered at 0, 1, and 6...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of medical virology 1986-07, Vol.19 (3), p.229-240
Hauptverfasser: Blaine Hollinger, F., Troisi, Catherine, Heiberg, Dorothy, Sanchez, Yanuario, Dreesman, Gordon R., Meinick, Joseph L.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 240
container_issue 3
container_start_page 229
container_title Journal of medical virology
container_volume 19
creator Blaine Hollinger, F.
Troisi, Catherine
Heiberg, Dorothy
Sanchez, Yanuario
Dreesman, Gordon R.
Meinick, Joseph L.
description Polypeptide micelles with relative molecular weights of 25,000 (p25) and 30,000 (gp30) daltons were prepared from native 22‐nm hepatitis B surface antigen (HBsAg) particles. This p25/gp30 complex was alum‐adsorbed, and three dosage levels (20 m̈g, 4 m̈g, and 0.8 m̈g) were administered at 0, 1, and 6 months to 51 human volunteers. Local and systemic reactions were clinically insignificant, and all vaccinees seroconverted, regardless of dose. As anticipated, antibody responses diminished as the dosage was reduced. Seroconversion rates and geometric mean antibody levels for the 20 m̈g dosage group were significantly better than those observed with a commercial vaccine and were comparable to those achieved after immunization with 40 m̈g of the intact 22‐nm particles used to prepare the polypeptides. By 2 weeks, an anti‐HBs response was elicited in 80% of the group receiving 20 m̈g of the polypeptide vaccine. This rapid response to immunization may be particularly beneficial for postexposure prophylaxis where the early development of immunity is advantageous.
doi_str_mv 10.1002/jmv.1890190305
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76963195</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76963195</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4385-4e0affbe47fc982a69dcc8e9a38adbc156a17746065bfd59b02b94ed8826e5ec3</originalsourceid><addsrcrecordid>eNqFkMtv1DAQxi0EKkvhyg3JB8Qtyzh-H6GiD1QeggLiZDnOBFySOMRJ6f73ZLWrRZx6Go3m930z8xHylMGaAZQvr7ubNTMWmAUO8h5ZMbCqsKDZfbICJlShFJMPyaOcrwHA2LI8IkelFaXiekW-f8I8pD4jnRL19CcOfopTzLSiQ2o3Aw5TrJHe-BBijzT2tIsB2xZpk8Zu23u6SXP_g_p6bqdFNMztYpH6x-RB49uMT_b1mHw5fXN1cl5cfji7OHl1WQTBjSwEgm-aCoVugjWlV7YOwaD13Pi6Ckwqz7QWCpSsmlraCsrKCqyNKRVKDPyYvNj5DmP6PWOeXBfz9kTfY5qz08oqzqy8E2RCANclLOB6B4Yx5Txi44Yxdn7cOAZuG7pbQnf_Ql8Ez_bOc9VhfcD3KS_z5_u5z8G3zej7EPMBM1ovz4gFszvsT2xxc8dS9_bd1_9OKHbamCe8PWj9-MspzbV0396fuY-n5-w1-3zlFP8LLLKqlg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>14403720</pqid></control><display><type>article</type><title>Response to a hepatitis b polypeptide vaccine in micelle form in a young adult population</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Blaine Hollinger, F. ; Troisi, Catherine ; Heiberg, Dorothy ; Sanchez, Yanuario ; Dreesman, Gordon R. ; Meinick, Joseph L.</creator><creatorcontrib>Blaine Hollinger, F. ; Troisi, Catherine ; Heiberg, Dorothy ; Sanchez, Yanuario ; Dreesman, Gordon R. ; Meinick, Joseph L.</creatorcontrib><description>Polypeptide micelles with relative molecular weights of 25,000 (p25) and 30,000 (gp30) daltons were prepared from native 22‐nm hepatitis B surface antigen (HBsAg) particles. This p25/gp30 complex was alum‐adsorbed, and three dosage levels (20 m̈g, 4 m̈g, and 0.8 m̈g) were administered at 0, 1, and 6 months to 51 human volunteers. Local and systemic reactions were clinically insignificant, and all vaccinees seroconverted, regardless of dose. As anticipated, antibody responses diminished as the dosage was reduced. Seroconversion rates and geometric mean antibody levels for the 20 m̈g dosage group were significantly better than those observed with a commercial vaccine and were comparable to those achieved after immunization with 40 m̈g of the intact 22‐nm particles used to prepare the polypeptides. By 2 weeks, an anti‐HBs response was elicited in 80% of the group receiving 20 m̈g of the polypeptide vaccine. This rapid response to immunization may be particularly beneficial for postexposure prophylaxis where the early development of immunity is advantageous.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.1890190305</identifier><identifier>PMID: 2942637</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Biological and medical sciences ; Female ; Hepatitis B Antibodies - analysis ; Hepatitis B Antibodies - biosynthesis ; Hepatitis B Surface Antigens - immunology ; hepatitis B vaccine ; Hepatitis B Vaccines ; hepatitis B virus ; Human viral diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Micelles ; Molecular Weight ; Peptides - immunology ; polypeptide vaccine ; prophylaxis of hepatitis B ; vaccine ; Viral diseases ; Viral hepatitis ; Viral Hepatitis Vaccines - administration &amp; dosage ; Viral Hepatitis Vaccines - immunology</subject><ispartof>Journal of medical virology, 1986-07, Vol.19 (3), p.229-240</ispartof><rights>Copyright © 1986 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4385-4e0affbe47fc982a69dcc8e9a38adbc156a17746065bfd59b02b94ed8826e5ec3</citedby><cites>FETCH-LOGICAL-c4385-4e0affbe47fc982a69dcc8e9a38adbc156a17746065bfd59b02b94ed8826e5ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.1890190305$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.1890190305$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=8778264$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2942637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Blaine Hollinger, F.</creatorcontrib><creatorcontrib>Troisi, Catherine</creatorcontrib><creatorcontrib>Heiberg, Dorothy</creatorcontrib><creatorcontrib>Sanchez, Yanuario</creatorcontrib><creatorcontrib>Dreesman, Gordon R.</creatorcontrib><creatorcontrib>Meinick, Joseph L.</creatorcontrib><title>Response to a hepatitis b polypeptide vaccine in micelle form in a young adult population</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>Polypeptide micelles with relative molecular weights of 25,000 (p25) and 30,000 (gp30) daltons were prepared from native 22‐nm hepatitis B surface antigen (HBsAg) particles. This p25/gp30 complex was alum‐adsorbed, and three dosage levels (20 m̈g, 4 m̈g, and 0.8 m̈g) were administered at 0, 1, and 6 months to 51 human volunteers. Local and systemic reactions were clinically insignificant, and all vaccinees seroconverted, regardless of dose. As anticipated, antibody responses diminished as the dosage was reduced. Seroconversion rates and geometric mean antibody levels for the 20 m̈g dosage group were significantly better than those observed with a commercial vaccine and were comparable to those achieved after immunization with 40 m̈g of the intact 22‐nm particles used to prepare the polypeptides. By 2 weeks, an anti‐HBs response was elicited in 80% of the group receiving 20 m̈g of the polypeptide vaccine. This rapid response to immunization may be particularly beneficial for postexposure prophylaxis where the early development of immunity is advantageous.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Hepatitis B Antibodies - analysis</subject><subject>Hepatitis B Antibodies - biosynthesis</subject><subject>Hepatitis B Surface Antigens - immunology</subject><subject>hepatitis B vaccine</subject><subject>Hepatitis B Vaccines</subject><subject>hepatitis B virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Micelles</subject><subject>Molecular Weight</subject><subject>Peptides - immunology</subject><subject>polypeptide vaccine</subject><subject>prophylaxis of hepatitis B</subject><subject>vaccine</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><subject>Viral Hepatitis Vaccines - administration &amp; dosage</subject><subject>Viral Hepatitis Vaccines - immunology</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtv1DAQxi0EKkvhyg3JB8Qtyzh-H6GiD1QeggLiZDnOBFySOMRJ6f73ZLWrRZx6Go3m930z8xHylMGaAZQvr7ubNTMWmAUO8h5ZMbCqsKDZfbICJlShFJMPyaOcrwHA2LI8IkelFaXiekW-f8I8pD4jnRL19CcOfopTzLSiQ2o3Aw5TrJHe-BBijzT2tIsB2xZpk8Zu23u6SXP_g_p6bqdFNMztYpH6x-RB49uMT_b1mHw5fXN1cl5cfji7OHl1WQTBjSwEgm-aCoVugjWlV7YOwaD13Pi6Ckwqz7QWCpSsmlraCsrKCqyNKRVKDPyYvNj5DmP6PWOeXBfz9kTfY5qz08oqzqy8E2RCANclLOB6B4Yx5Txi44Yxdn7cOAZuG7pbQnf_Ql8Ez_bOc9VhfcD3KS_z5_u5z8G3zej7EPMBM1ovz4gFszvsT2xxc8dS9_bd1_9OKHbamCe8PWj9-MspzbV0396fuY-n5-w1-3zlFP8LLLKqlg</recordid><startdate>198607</startdate><enddate>198607</enddate><creator>Blaine Hollinger, F.</creator><creator>Troisi, Catherine</creator><creator>Heiberg, Dorothy</creator><creator>Sanchez, Yanuario</creator><creator>Dreesman, Gordon R.</creator><creator>Meinick, Joseph L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>198607</creationdate><title>Response to a hepatitis b polypeptide vaccine in micelle form in a young adult population</title><author>Blaine Hollinger, F. ; Troisi, Catherine ; Heiberg, Dorothy ; Sanchez, Yanuario ; Dreesman, Gordon R. ; Meinick, Joseph L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4385-4e0affbe47fc982a69dcc8e9a38adbc156a17746065bfd59b02b94ed8826e5ec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Hepatitis B Antibodies - analysis</topic><topic>Hepatitis B Antibodies - biosynthesis</topic><topic>Hepatitis B Surface Antigens - immunology</topic><topic>hepatitis B vaccine</topic><topic>Hepatitis B Vaccines</topic><topic>hepatitis B virus</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Micelles</topic><topic>Molecular Weight</topic><topic>Peptides - immunology</topic><topic>polypeptide vaccine</topic><topic>prophylaxis of hepatitis B</topic><topic>vaccine</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><topic>Viral Hepatitis Vaccines - administration &amp; dosage</topic><topic>Viral Hepatitis Vaccines - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blaine Hollinger, F.</creatorcontrib><creatorcontrib>Troisi, Catherine</creatorcontrib><creatorcontrib>Heiberg, Dorothy</creatorcontrib><creatorcontrib>Sanchez, Yanuario</creatorcontrib><creatorcontrib>Dreesman, Gordon R.</creatorcontrib><creatorcontrib>Meinick, Joseph L.</creatorcontrib><collection>Istex</collection><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>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blaine Hollinger, F.</au><au>Troisi, Catherine</au><au>Heiberg, Dorothy</au><au>Sanchez, Yanuario</au><au>Dreesman, Gordon R.</au><au>Meinick, Joseph L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Response to a hepatitis b polypeptide vaccine in micelle form in a young adult population</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. Med. Virol</addtitle><date>1986-07</date><risdate>1986</risdate><volume>19</volume><issue>3</issue><spage>229</spage><epage>240</epage><pages>229-240</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><coden>JMVIDB</coden><abstract>Polypeptide micelles with relative molecular weights of 25,000 (p25) and 30,000 (gp30) daltons were prepared from native 22‐nm hepatitis B surface antigen (HBsAg) particles. This p25/gp30 complex was alum‐adsorbed, and three dosage levels (20 m̈g, 4 m̈g, and 0.8 m̈g) were administered at 0, 1, and 6 months to 51 human volunteers. Local and systemic reactions were clinically insignificant, and all vaccinees seroconverted, regardless of dose. As anticipated, antibody responses diminished as the dosage was reduced. Seroconversion rates and geometric mean antibody levels for the 20 m̈g dosage group were significantly better than those observed with a commercial vaccine and were comparable to those achieved after immunization with 40 m̈g of the intact 22‐nm particles used to prepare the polypeptides. By 2 weeks, an anti‐HBs response was elicited in 80% of the group receiving 20 m̈g of the polypeptide vaccine. This rapid response to immunization may be particularly beneficial for postexposure prophylaxis where the early development of immunity is advantageous.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2942637</pmid><doi>10.1002/jmv.1890190305</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0146-6615
ispartof Journal of medical virology, 1986-07, Vol.19 (3), p.229-240
issn 0146-6615
1096-9071
language eng
recordid cdi_proquest_miscellaneous_76963195
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Adult
Biological and medical sciences
Female
Hepatitis B Antibodies - analysis
Hepatitis B Antibodies - biosynthesis
Hepatitis B Surface Antigens - immunology
hepatitis B vaccine
Hepatitis B Vaccines
hepatitis B virus
Human viral diseases
Humans
Infectious diseases
Male
Medical sciences
Micelles
Molecular Weight
Peptides - immunology
polypeptide vaccine
prophylaxis of hepatitis B
vaccine
Viral diseases
Viral hepatitis
Viral Hepatitis Vaccines - administration & dosage
Viral Hepatitis Vaccines - immunology
title Response to a hepatitis b polypeptide vaccine in micelle form in a young adult population
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T15%3A01%3A09IST&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=Response%20to%20a%20hepatitis%20b%20polypeptide%20vaccine%20in%20micelle%20form%20in%20a%20young%20adult%20population&rft.jtitle=Journal%20of%20medical%20virology&rft.au=Blaine%20Hollinger,%20F.&rft.date=1986-07&rft.volume=19&rft.issue=3&rft.spage=229&rft.epage=240&rft.pages=229-240&rft.issn=0146-6615&rft.eissn=1096-9071&rft.coden=JMVIDB&rft_id=info:doi/10.1002/jmv.1890190305&rft_dat=%3Cproquest_cross%3E76963195%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=14403720&rft_id=info:pmid/2942637&rfr_iscdi=true