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...
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Veröffentlicht in: | Journal of medical virology 1986-07, Vol.19 (3), p.229-240 |
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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 |
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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 & 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&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 & 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 & 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> |
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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 |
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