Vaccines against human papillomavirus infections: protection against cancer, genital warts or both?

Since 2006, three vaccines against infections and disease caused by human papillomavirus (HPV) became available in Europe—in 2006 a quadrivalent HPV 6/11/16/18 vaccine, in 2007 a bivalent HPV 16/18 vaccine and in 2015 a nonavalent HPV 6/11/16/18/31/33/45/52/58 vaccine. HPV 16 and 18 are the most onc...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Clinical microbiology and infection 2016-12, Vol.22, p.S125-S127
Hauptverfasser: Joura, E.A., Pils, S.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page S127
container_issue
container_start_page S125
container_title Clinical microbiology and infection
container_volume 22
creator Joura, E.A.
Pils, S.
description Since 2006, three vaccines against infections and disease caused by human papillomavirus (HPV) became available in Europe—in 2006 a quadrivalent HPV 6/11/16/18 vaccine, in 2007 a bivalent HPV 16/18 vaccine and in 2015 a nonavalent HPV 6/11/16/18/31/33/45/52/58 vaccine. HPV 16 and 18 are the most oncogenic HPV strains, causing about 70% of cervical and other HPV-related cancers, HPV 6 and 11 cause 85% of all genital warts. The additional types of the polyvalent vaccine account for about 20% of invasive cervical cancer and >35% of pre-cancer. The potential differences between these vaccines caused some debate. All three vaccines give a robust and long-lasting protection against the strains in the various vaccines. The promise of cross-protection against other types (i.e. HPV 31/33/45) and hence a broader cancer protection was not fulfilled because these observations were confounded by the vaccine efficacy against the vaccine types. Furthermore, cross-protection was not consistent over various studies, not durable and not consistently seen in the real world experience. The protection against disease caused by oncogenic HPV strains was not compromised by the protection against low-risk types causing genital warts. The most effective cancer protection to date can be expected by the nonavalent vaccine, data indicate a 97% efficacy against cervical and vulvovaginal pre-cancer caused by these nine HPV types.
doi_str_mv 10.1016/j.cmi.2016.12.017
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1854620036</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1198743X16306346</els_id><sourcerecordid>1854620036</sourcerecordid><originalsourceid>FETCH-LOGICAL-c396t-64794a0a2d889ccc1047f632ec6bdbf8987534bd891f0933d38801df18d043f33</originalsourceid><addsrcrecordid>eNp9kEtLBDEQhIMo7vr4AV4kRw_OmJ5kM4keRBZfsOBFxVvIJBnNMo81mVH892ZZ9eipq6Gq6P4QOgKSAwF-tsxN6_MiyRyKnEC5habAuMwIl7CdNEiRlYy-TNBejEtCSEEp20WTQhDKaAlTZJ61Mb5zEetX7bs44Lex1R1e6ZVvmr7VHz6MEfuudmbwfRfP8Sr0w2b5yxjdGRdO8avr_KAb_KnDEHEfcNUPb5cHaKfWTXSHP3MfPd1cP87vssXD7f38apEZKvmQcVZKpokurBDSGAOElTWnhTO8slUtpChnlFVWSKiJpNRSIQjYGoQljNaU7qOTTW-68H10cVCtj8Y1je5cP0YFYsZ4QQjlyQobqwl9jMHVahV8q8OXAqLWbNVSJbZqzVZBoRLblDn-qR-r1tm_xC_MZLjYGFx68sO7oKLxLpGxPiRgyvb-n_pvEqOKqA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1854620036</pqid></control><display><type>article</type><title>Vaccines against human papillomavirus infections: protection against cancer, genital warts or both?</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Joura, E.A. ; Pils, S.</creator><creatorcontrib>Joura, E.A. ; Pils, S.</creatorcontrib><description>Since 2006, three vaccines against infections and disease caused by human papillomavirus (HPV) became available in Europe—in 2006 a quadrivalent HPV 6/11/16/18 vaccine, in 2007 a bivalent HPV 16/18 vaccine and in 2015 a nonavalent HPV 6/11/16/18/31/33/45/52/58 vaccine. HPV 16 and 18 are the most oncogenic HPV strains, causing about 70% of cervical and other HPV-related cancers, HPV 6 and 11 cause 85% of all genital warts. The additional types of the polyvalent vaccine account for about 20% of invasive cervical cancer and &gt;35% of pre-cancer. The potential differences between these vaccines caused some debate. All three vaccines give a robust and long-lasting protection against the strains in the various vaccines. The promise of cross-protection against other types (i.e. HPV 31/33/45) and hence a broader cancer protection was not fulfilled because these observations were confounded by the vaccine efficacy against the vaccine types. Furthermore, cross-protection was not consistent over various studies, not durable and not consistently seen in the real world experience. The protection against disease caused by oncogenic HPV strains was not compromised by the protection against low-risk types causing genital warts. The most effective cancer protection to date can be expected by the nonavalent vaccine, data indicate a 97% efficacy against cervical and vulvovaginal pre-cancer caused by these nine HPV types.</description><identifier>ISSN: 1198-743X</identifier><identifier>EISSN: 1469-0691</identifier><identifier>DOI: 10.1016/j.cmi.2016.12.017</identifier><identifier>PMID: 28034371</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Cervical cancer ; Condylomata Acuminata - prevention &amp; control ; Female ; Genital warts ; Human papillomavirus ; Humans ; Papillomaviridae - immunology ; Papillomavirus Vaccines - immunology ; Uterine Cervical Neoplasms - prevention &amp; control ; Uterine Cervical Neoplasms - virology ; Vaccine ; Vulvar cancer ; Vulvar Neoplasms - prevention &amp; control ; Vulvar Neoplasms - virology</subject><ispartof>Clinical microbiology and infection, 2016-12, Vol.22, p.S125-S127</ispartof><rights>2016 European Society of Clinical Microbiology and Infectious Diseases</rights><rights>Copyright © 2016 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-64794a0a2d889ccc1047f632ec6bdbf8987534bd891f0933d38801df18d043f33</citedby><cites>FETCH-LOGICAL-c396t-64794a0a2d889ccc1047f632ec6bdbf8987534bd891f0933d38801df18d043f33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28034371$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joura, E.A.</creatorcontrib><creatorcontrib>Pils, S.</creatorcontrib><title>Vaccines against human papillomavirus infections: protection against cancer, genital warts or both?</title><title>Clinical microbiology and infection</title><addtitle>Clin Microbiol Infect</addtitle><description>Since 2006, three vaccines against infections and disease caused by human papillomavirus (HPV) became available in Europe—in 2006 a quadrivalent HPV 6/11/16/18 vaccine, in 2007 a bivalent HPV 16/18 vaccine and in 2015 a nonavalent HPV 6/11/16/18/31/33/45/52/58 vaccine. HPV 16 and 18 are the most oncogenic HPV strains, causing about 70% of cervical and other HPV-related cancers, HPV 6 and 11 cause 85% of all genital warts. The additional types of the polyvalent vaccine account for about 20% of invasive cervical cancer and &gt;35% of pre-cancer. The potential differences between these vaccines caused some debate. All three vaccines give a robust and long-lasting protection against the strains in the various vaccines. The promise of cross-protection against other types (i.e. HPV 31/33/45) and hence a broader cancer protection was not fulfilled because these observations were confounded by the vaccine efficacy against the vaccine types. Furthermore, cross-protection was not consistent over various studies, not durable and not consistently seen in the real world experience. The protection against disease caused by oncogenic HPV strains was not compromised by the protection against low-risk types causing genital warts. The most effective cancer protection to date can be expected by the nonavalent vaccine, data indicate a 97% efficacy against cervical and vulvovaginal pre-cancer caused by these nine HPV types.</description><subject>Cervical cancer</subject><subject>Condylomata Acuminata - prevention &amp; control</subject><subject>Female</subject><subject>Genital warts</subject><subject>Human papillomavirus</subject><subject>Humans</subject><subject>Papillomaviridae - immunology</subject><subject>Papillomavirus Vaccines - immunology</subject><subject>Uterine Cervical Neoplasms - prevention &amp; control</subject><subject>Uterine Cervical Neoplasms - virology</subject><subject>Vaccine</subject><subject>Vulvar cancer</subject><subject>Vulvar Neoplasms - prevention &amp; control</subject><subject>Vulvar Neoplasms - virology</subject><issn>1198-743X</issn><issn>1469-0691</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLBDEQhIMo7vr4AV4kRw_OmJ5kM4keRBZfsOBFxVvIJBnNMo81mVH892ZZ9eipq6Gq6P4QOgKSAwF-tsxN6_MiyRyKnEC5habAuMwIl7CdNEiRlYy-TNBejEtCSEEp20WTQhDKaAlTZJ61Mb5zEetX7bs44Lex1R1e6ZVvmr7VHz6MEfuudmbwfRfP8Sr0w2b5yxjdGRdO8avr_KAb_KnDEHEfcNUPb5cHaKfWTXSHP3MfPd1cP87vssXD7f38apEZKvmQcVZKpokurBDSGAOElTWnhTO8slUtpChnlFVWSKiJpNRSIQjYGoQljNaU7qOTTW-68H10cVCtj8Y1je5cP0YFYsZ4QQjlyQobqwl9jMHVahV8q8OXAqLWbNVSJbZqzVZBoRLblDn-qR-r1tm_xC_MZLjYGFx68sO7oKLxLpGxPiRgyvb-n_pvEqOKqA</recordid><startdate>20161201</startdate><enddate>20161201</enddate><creator>Joura, E.A.</creator><creator>Pils, S.</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope></search><sort><creationdate>20161201</creationdate><title>Vaccines against human papillomavirus infections: protection against cancer, genital warts or both?</title><author>Joura, E.A. ; Pils, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-64794a0a2d889ccc1047f632ec6bdbf8987534bd891f0933d38801df18d043f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cervical cancer</topic><topic>Condylomata Acuminata - prevention &amp; control</topic><topic>Female</topic><topic>Genital warts</topic><topic>Human papillomavirus</topic><topic>Humans</topic><topic>Papillomaviridae - immunology</topic><topic>Papillomavirus Vaccines - immunology</topic><topic>Uterine Cervical Neoplasms - prevention &amp; control</topic><topic>Uterine Cervical Neoplasms - virology</topic><topic>Vaccine</topic><topic>Vulvar cancer</topic><topic>Vulvar Neoplasms - prevention &amp; control</topic><topic>Vulvar Neoplasms - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joura, E.A.</creatorcontrib><creatorcontrib>Pils, S.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical microbiology and infection</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joura, E.A.</au><au>Pils, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vaccines against human papillomavirus infections: protection against cancer, genital warts or both?</atitle><jtitle>Clinical microbiology and infection</jtitle><addtitle>Clin Microbiol Infect</addtitle><date>2016-12-01</date><risdate>2016</risdate><volume>22</volume><spage>S125</spage><epage>S127</epage><pages>S125-S127</pages><issn>1198-743X</issn><eissn>1469-0691</eissn><abstract>Since 2006, three vaccines against infections and disease caused by human papillomavirus (HPV) became available in Europe—in 2006 a quadrivalent HPV 6/11/16/18 vaccine, in 2007 a bivalent HPV 16/18 vaccine and in 2015 a nonavalent HPV 6/11/16/18/31/33/45/52/58 vaccine. HPV 16 and 18 are the most oncogenic HPV strains, causing about 70% of cervical and other HPV-related cancers, HPV 6 and 11 cause 85% of all genital warts. The additional types of the polyvalent vaccine account for about 20% of invasive cervical cancer and &gt;35% of pre-cancer. The potential differences between these vaccines caused some debate. All three vaccines give a robust and long-lasting protection against the strains in the various vaccines. The promise of cross-protection against other types (i.e. HPV 31/33/45) and hence a broader cancer protection was not fulfilled because these observations were confounded by the vaccine efficacy against the vaccine types. Furthermore, cross-protection was not consistent over various studies, not durable and not consistently seen in the real world experience. The protection against disease caused by oncogenic HPV strains was not compromised by the protection against low-risk types causing genital warts. The most effective cancer protection to date can be expected by the nonavalent vaccine, data indicate a 97% efficacy against cervical and vulvovaginal pre-cancer caused by these nine HPV types.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28034371</pmid><doi>10.1016/j.cmi.2016.12.017</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1198-743X
ispartof Clinical microbiology and infection, 2016-12, Vol.22, p.S125-S127
issn 1198-743X
1469-0691
language eng
recordid cdi_proquest_miscellaneous_1854620036
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Cervical cancer
Condylomata Acuminata - prevention & control
Female
Genital warts
Human papillomavirus
Humans
Papillomaviridae - immunology
Papillomavirus Vaccines - immunology
Uterine Cervical Neoplasms - prevention & control
Uterine Cervical Neoplasms - virology
Vaccine
Vulvar cancer
Vulvar Neoplasms - prevention & control
Vulvar Neoplasms - virology
title Vaccines against human papillomavirus infections: protection against cancer, genital warts or both?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T02%3A10%3A29IST&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=Vaccines%20against%20human%20papillomavirus%20infections:%20protection%20against%20cancer,%20genital%20warts%20or%20both?&rft.jtitle=Clinical%20microbiology%20and%20infection&rft.au=Joura,%20E.A.&rft.date=2016-12-01&rft.volume=22&rft.spage=S125&rft.epage=S127&rft.pages=S125-S127&rft.issn=1198-743X&rft.eissn=1469-0691&rft_id=info:doi/10.1016/j.cmi.2016.12.017&rft_dat=%3Cproquest_cross%3E1854620036%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=1854620036&rft_id=info:pmid/28034371&rft_els_id=S1198743X16306346&rfr_iscdi=true