Immunogenicity of New Primary Immunization Schedules With Inactivated Poliovirus Vaccine and Bivalent Oral Polio Vaccine for the Polio Endgame: A Review
Abstract In May 2016, countries using oral polio vaccine for routine immunization switched from trivalent oral poliovirus vaccine (tOPV) to bivalent type 1 and 3 OPV (bOPV). This was done in order to reduce risks from type 2 vaccine-derived polioviruses (VDPV2) and vaccine-associated paralytic polio...
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Veröffentlicht in: | Clinical infectious diseases 2018-10, Vol.67 (suppl_1), p.S35-S41 |
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creator | Bandyopadhyay, Ananda S Modlin, John F Wenger, Jay Gast, Chris |
description | Abstract
In May 2016, countries using oral polio vaccine for routine immunization switched from trivalent oral poliovirus vaccine (tOPV) to bivalent type 1 and 3 OPV (bOPV). This was done in order to reduce risks from type 2 vaccine-derived polioviruses (VDPV2) and vaccine-associated paralytic poliomyelitis (VAPP) and to introduce ≥1 dose of inactivated poliovirus vaccine (IPV) to mitigate post-switch loss of type 2 immunity. We conducted a literature review of studies that assessed humoral and intestinal immunogenicity induced by the newly recommended schedules. Differences in seroconversion rates were closely associated with both timing of first IPV administration and number of doses administered. All studies demonstrated high levels of immunity for types 1 and 3 regardless of immunization schedule. When administered late in the primary series, a second dose of IPV closed the humoral immunity gap against polio type 2 associated with a single dose. IPV doses and administration schedules appear to have limited impact on type 2 excretion following challenge. |
doi_str_mv | 10.1093/cid/ciy633 |
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In May 2016, countries using oral polio vaccine for routine immunization switched from trivalent oral poliovirus vaccine (tOPV) to bivalent type 1 and 3 OPV (bOPV). This was done in order to reduce risks from type 2 vaccine-derived polioviruses (VDPV2) and vaccine-associated paralytic poliomyelitis (VAPP) and to introduce ≥1 dose of inactivated poliovirus vaccine (IPV) to mitigate post-switch loss of type 2 immunity. We conducted a literature review of studies that assessed humoral and intestinal immunogenicity induced by the newly recommended schedules. Differences in seroconversion rates were closely associated with both timing of first IPV administration and number of doses administered. All studies demonstrated high levels of immunity for types 1 and 3 regardless of immunization schedule. When administered late in the primary series, a second dose of IPV closed the humoral immunity gap against polio type 2 associated with a single dose. IPV doses and administration schedules appear to have limited impact on type 2 excretion following challenge.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/ciy633</identifier><identifier>PMID: 30376081</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Supplement</subject><ispartof>Clinical infectious diseases, 2018-10, Vol.67 (suppl_1), p.S35-S41</ispartof><rights>The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-77cde3c83c39d480e4f742412c14ab41d95b5372a1655e8824379ddd63981d1b3</citedby><cites>FETCH-LOGICAL-c408t-77cde3c83c39d480e4f742412c14ab41d95b5372a1655e8824379ddd63981d1b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30376081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bandyopadhyay, Ananda S</creatorcontrib><creatorcontrib>Modlin, John F</creatorcontrib><creatorcontrib>Wenger, Jay</creatorcontrib><creatorcontrib>Gast, Chris</creatorcontrib><title>Immunogenicity of New Primary Immunization Schedules With Inactivated Poliovirus Vaccine and Bivalent Oral Polio Vaccine for the Polio Endgame: A Review</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Abstract
In May 2016, countries using oral polio vaccine for routine immunization switched from trivalent oral poliovirus vaccine (tOPV) to bivalent type 1 and 3 OPV (bOPV). This was done in order to reduce risks from type 2 vaccine-derived polioviruses (VDPV2) and vaccine-associated paralytic poliomyelitis (VAPP) and to introduce ≥1 dose of inactivated poliovirus vaccine (IPV) to mitigate post-switch loss of type 2 immunity. We conducted a literature review of studies that assessed humoral and intestinal immunogenicity induced by the newly recommended schedules. Differences in seroconversion rates were closely associated with both timing of first IPV administration and number of doses administered. All studies demonstrated high levels of immunity for types 1 and 3 regardless of immunization schedule. When administered late in the primary series, a second dose of IPV closed the humoral immunity gap against polio type 2 associated with a single dose. IPV doses and administration schedules appear to have limited impact on type 2 excretion following challenge.</description><subject>Supplement</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kV9rFDEUxYNY7D9f_ACSF0EKY5NJJpPxQail6kKxRW19DNnkzm5kJlknmS3rJ_HjNnbWRV_6EBJyfpx7uAehF5S8oaRhp8bZfDaCsSfogFasLkTV0Kf5TSpZcMnkPjqM8QchlEpSPUP7jLBaEEkP0O9Z348-LMA749IGhxZ_hjt8PbheDxv8oLpfOrng8VezBDt2EPF3l5Z45rVJbq0TWHwdOhfWbhgjvtXGOA9Ye4vfZ7kDn_DVoLsJ2ultGHBawvb3wtuF7uEtPsNfYO3g7hjttbqL8Hx7H6GbDxffzj8Vl1cfZ-dnl4XhRKairo0FZiQzrLFcEuBtzUtOS0O5nnNqm2qeN1JqKqoKpCw5qxtrrWCNpJbO2RF6N_muxnkP1uS0OataTQtQQTv1v-LdUi3CWomSCFpW2eD11mAIP0eISfUuGug67SGMUZW0rGkjRMMyejKhZggxDtDuxlCi_lSpcpVqqjLDL_8NtkP_dpeBVxMQxtVjRveIpaoX</recordid><startdate>20181030</startdate><enddate>20181030</enddate><creator>Bandyopadhyay, Ananda S</creator><creator>Modlin, John F</creator><creator>Wenger, Jay</creator><creator>Gast, Chris</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20181030</creationdate><title>Immunogenicity of New Primary Immunization Schedules With Inactivated Poliovirus Vaccine and Bivalent Oral Polio Vaccine for the Polio Endgame: A Review</title><author>Bandyopadhyay, Ananda S ; Modlin, John F ; Wenger, Jay ; Gast, Chris</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-77cde3c83c39d480e4f742412c14ab41d95b5372a1655e8824379ddd63981d1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Supplement</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bandyopadhyay, Ananda S</creatorcontrib><creatorcontrib>Modlin, John F</creatorcontrib><creatorcontrib>Wenger, Jay</creatorcontrib><creatorcontrib>Gast, Chris</creatorcontrib><collection>Oxford Open</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bandyopadhyay, Ananda S</au><au>Modlin, John F</au><au>Wenger, Jay</au><au>Gast, Chris</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunogenicity of New Primary Immunization Schedules With Inactivated Poliovirus Vaccine and Bivalent Oral Polio Vaccine for the Polio Endgame: A Review</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2018-10-30</date><risdate>2018</risdate><volume>67</volume><issue>suppl_1</issue><spage>S35</spage><epage>S41</epage><pages>S35-S41</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>Abstract
In May 2016, countries using oral polio vaccine for routine immunization switched from trivalent oral poliovirus vaccine (tOPV) to bivalent type 1 and 3 OPV (bOPV). This was done in order to reduce risks from type 2 vaccine-derived polioviruses (VDPV2) and vaccine-associated paralytic poliomyelitis (VAPP) and to introduce ≥1 dose of inactivated poliovirus vaccine (IPV) to mitigate post-switch loss of type 2 immunity. We conducted a literature review of studies that assessed humoral and intestinal immunogenicity induced by the newly recommended schedules. Differences in seroconversion rates were closely associated with both timing of first IPV administration and number of doses administered. All studies demonstrated high levels of immunity for types 1 and 3 regardless of immunization schedule. When administered late in the primary series, a second dose of IPV closed the humoral immunity gap against polio type 2 associated with a single dose. IPV doses and administration schedules appear to have limited impact on type 2 excretion following challenge.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>30376081</pmid><doi>10.1093/cid/ciy633</doi><oa>free_for_read</oa></addata></record> |
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title | Immunogenicity of New Primary Immunization Schedules With Inactivated Poliovirus Vaccine and Bivalent Oral Polio Vaccine for the Polio Endgame: A Review |
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