The Origins and Risk Factors for Serotype-2 Vaccine-Derived Poliovirus Emergences in Africa During 2016–2019
Abstract Serotype 2 oral poliovirus vaccine (OPV2) can revert to regain wild-type neurovirulence and spread to cause emergences of vaccine-derived poliovirus (VDPV2). After its global withdrawal from routine immunization in 2016, outbreak response use has created a cycle of VDPV2 emergences that thr...
Gespeichert in:
Veröffentlicht in: | The Journal of infectious diseases 2023-06, Vol.228 (1), p.80-88 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 88 |
---|---|
container_issue | 1 |
container_start_page | 80 |
container_title | The Journal of infectious diseases |
container_volume | 228 |
creator | Gray, Elizabeth J Cooper, Laura V Bandyopadhyay, Ananda S Blake, Isobel M Grassly, Nicholas C |
description | Abstract
Serotype 2 oral poliovirus vaccine (OPV2) can revert to regain wild-type neurovirulence and spread to cause emergences of vaccine-derived poliovirus (VDPV2). After its global withdrawal from routine immunization in 2016, outbreak response use has created a cycle of VDPV2 emergences that threaten eradication. We implemented a hierarchical model based on VP1 region genetic divergence, time, and location to attribute emergences to campaigns and identify risk factors. We found that a 10 percentage point increase in population immunity in children younger than 5 years at the campaign time and location corresponds to a 18.0% decrease (95% credible interval [CrI], 6.3%–28%) in per-campaign relative risk, and that campaign size is associated with emergence risk (relative risk scaling with population size to a power of 0.80; 95% CrI, .50–1.10). Our results imply how Sabin OPV2 can be used alongside the genetically stable but supply-limited novel OPV2 (listed for emergency use in November 2020) to minimize emergence risk.
Outbreaks of vaccine-derived poliovirus from rare reversion of type-2 Sabin vaccine strain inhibit polio eradication efforts. We use a hierarchical model, incorporating VP1 region genetic divergence and population movement, to estimate outbreak origins and risk factors for vaccine campaigns. |
doi_str_mv | 10.1093/infdis/jiad004 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10304761</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/infdis/jiad004</oup_id><sourcerecordid>3051851302</sourcerecordid><originalsourceid>FETCH-LOGICAL-c453t-416b6667ee70e300993f90c0ddcf33f3bebe614e6a1d12507f78b42000c9c87a3</originalsourceid><addsrcrecordid>eNqFkT9vFDEQxS0EIpeDlhJZooFik_F61z5XKMofQIoUBIHW8nrHFx979sXePSldvgPfkE-C0R0R0FBNMb95mvceIS8YHDFQ_NgH1_t8vPKmB2gekRlruayEYPwxmQHUdcUWSh2Qw5xXUAgu5FNywIXgUKt2RsL1DdKr5Jc-ZGpCTz_5_I1eGDvGlKmLiX7GFMe7DVY1_Wqs9QGrM0x-iz39GAcftz5NmZ6vMS0xWMzUB3rikreGnk3JhyWtgYkf99_LUM_IE2eGjM_3c06-XJxfn76vLq_efTg9uaxs0_KxapjohBASUQJyAKW4U2Ch763j3PEOOxSsQWFYz-oWpJOLrqmLQavsQho-J293upupW2NvMYzJDHqT_NqkOx2N139vgr_Ry7jVDDg0ssQ3J6_3CineTphHvfbZ4jCYgHHKupaiaRrGFC_oq3_QVZxSKP40h5YtWlbCLtTRjrIp5pzQPXzDQP_qUu-61Psuy8HLPz084L_LK8CbHRCnzf_EfgLOn6qP</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3051851302</pqid></control><display><type>article</type><title>The Origins and Risk Factors for Serotype-2 Vaccine-Derived Poliovirus Emergences in Africa During 2016–2019</title><source>Oxford University Press Journals All Titles (1996-Current)</source><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Gray, Elizabeth J ; Cooper, Laura V ; Bandyopadhyay, Ananda S ; Blake, Isobel M ; Grassly, Nicholas C</creator><creatorcontrib>Gray, Elizabeth J ; Cooper, Laura V ; Bandyopadhyay, Ananda S ; Blake, Isobel M ; Grassly, Nicholas C</creatorcontrib><description>Abstract
Serotype 2 oral poliovirus vaccine (OPV2) can revert to regain wild-type neurovirulence and spread to cause emergences of vaccine-derived poliovirus (VDPV2). After its global withdrawal from routine immunization in 2016, outbreak response use has created a cycle of VDPV2 emergences that threaten eradication. We implemented a hierarchical model based on VP1 region genetic divergence, time, and location to attribute emergences to campaigns and identify risk factors. We found that a 10 percentage point increase in population immunity in children younger than 5 years at the campaign time and location corresponds to a 18.0% decrease (95% credible interval [CrI], 6.3%–28%) in per-campaign relative risk, and that campaign size is associated with emergence risk (relative risk scaling with population size to a power of 0.80; 95% CrI, .50–1.10). Our results imply how Sabin OPV2 can be used alongside the genetically stable but supply-limited novel OPV2 (listed for emergency use in November 2020) to minimize emergence risk.
Outbreaks of vaccine-derived poliovirus from rare reversion of type-2 Sabin vaccine strain inhibit polio eradication efforts. We use a hierarchical model, incorporating VP1 region genetic divergence and population movement, to estimate outbreak origins and risk factors for vaccine campaigns.</description><identifier>ISSN: 0022-1899</identifier><identifier>ISSN: 1537-6613</identifier><identifier>EISSN: 1537-6613</identifier><identifier>DOI: 10.1093/infdis/jiad004</identifier><identifier>PMID: 36630295</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Africa - epidemiology ; Child ; Disease Outbreaks - prevention & control ; Genetic divergence ; Herd immunity ; Humans ; Immunization ; Major ; Neurovirulence ; Poliomyelitis - epidemiology ; Poliomyelitis - prevention & control ; Poliovirus - genetics ; Poliovirus Vaccine, Oral - adverse effects ; Risk Factors ; Serogroup ; Vaccines</subject><ispartof>The Journal of infectious diseases, 2023-06, Vol.228 (1), p.80-88</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2023</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-416b6667ee70e300993f90c0ddcf33f3bebe614e6a1d12507f78b42000c9c87a3</citedby><cites>FETCH-LOGICAL-c453t-416b6667ee70e300993f90c0ddcf33f3bebe614e6a1d12507f78b42000c9c87a3</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/36630295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gray, Elizabeth J</creatorcontrib><creatorcontrib>Cooper, Laura V</creatorcontrib><creatorcontrib>Bandyopadhyay, Ananda S</creatorcontrib><creatorcontrib>Blake, Isobel M</creatorcontrib><creatorcontrib>Grassly, Nicholas C</creatorcontrib><title>The Origins and Risk Factors for Serotype-2 Vaccine-Derived Poliovirus Emergences in Africa During 2016–2019</title><title>The Journal of infectious diseases</title><addtitle>J Infect Dis</addtitle><description>Abstract
Serotype 2 oral poliovirus vaccine (OPV2) can revert to regain wild-type neurovirulence and spread to cause emergences of vaccine-derived poliovirus (VDPV2). After its global withdrawal from routine immunization in 2016, outbreak response use has created a cycle of VDPV2 emergences that threaten eradication. We implemented a hierarchical model based on VP1 region genetic divergence, time, and location to attribute emergences to campaigns and identify risk factors. We found that a 10 percentage point increase in population immunity in children younger than 5 years at the campaign time and location corresponds to a 18.0% decrease (95% credible interval [CrI], 6.3%–28%) in per-campaign relative risk, and that campaign size is associated with emergence risk (relative risk scaling with population size to a power of 0.80; 95% CrI, .50–1.10). Our results imply how Sabin OPV2 can be used alongside the genetically stable but supply-limited novel OPV2 (listed for emergency use in November 2020) to minimize emergence risk.
Outbreaks of vaccine-derived poliovirus from rare reversion of type-2 Sabin vaccine strain inhibit polio eradication efforts. We use a hierarchical model, incorporating VP1 region genetic divergence and population movement, to estimate outbreak origins and risk factors for vaccine campaigns.</description><subject>Africa - epidemiology</subject><subject>Child</subject><subject>Disease Outbreaks - prevention & control</subject><subject>Genetic divergence</subject><subject>Herd immunity</subject><subject>Humans</subject><subject>Immunization</subject><subject>Major</subject><subject>Neurovirulence</subject><subject>Poliomyelitis - epidemiology</subject><subject>Poliomyelitis - prevention & control</subject><subject>Poliovirus - genetics</subject><subject>Poliovirus Vaccine, Oral - adverse effects</subject><subject>Risk Factors</subject><subject>Serogroup</subject><subject>Vaccines</subject><issn>0022-1899</issn><issn>1537-6613</issn><issn>1537-6613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNqFkT9vFDEQxS0EIpeDlhJZooFik_F61z5XKMofQIoUBIHW8nrHFx979sXePSldvgPfkE-C0R0R0FBNMb95mvceIS8YHDFQ_NgH1_t8vPKmB2gekRlruayEYPwxmQHUdcUWSh2Qw5xXUAgu5FNywIXgUKt2RsL1DdKr5Jc-ZGpCTz_5_I1eGDvGlKmLiX7GFMe7DVY1_Wqs9QGrM0x-iz39GAcftz5NmZ6vMS0xWMzUB3rikreGnk3JhyWtgYkf99_LUM_IE2eGjM_3c06-XJxfn76vLq_efTg9uaxs0_KxapjohBASUQJyAKW4U2Ch763j3PEOOxSsQWFYz-oWpJOLrqmLQavsQho-J293upupW2NvMYzJDHqT_NqkOx2N139vgr_Ry7jVDDg0ssQ3J6_3CineTphHvfbZ4jCYgHHKupaiaRrGFC_oq3_QVZxSKP40h5YtWlbCLtTRjrIp5pzQPXzDQP_qUu-61Psuy8HLPz084L_LK8CbHRCnzf_EfgLOn6qP</recordid><startdate>20230628</startdate><enddate>20230628</enddate><creator>Gray, Elizabeth J</creator><creator>Cooper, Laura V</creator><creator>Bandyopadhyay, Ananda S</creator><creator>Blake, Isobel M</creator><creator>Grassly, Nicholas C</creator><general>Oxford University Press</general><scope>TOX</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>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20230628</creationdate><title>The Origins and Risk Factors for Serotype-2 Vaccine-Derived Poliovirus Emergences in Africa During 2016–2019</title><author>Gray, Elizabeth J ; Cooper, Laura V ; Bandyopadhyay, Ananda S ; Blake, Isobel M ; Grassly, Nicholas C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-416b6667ee70e300993f90c0ddcf33f3bebe614e6a1d12507f78b42000c9c87a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Africa - epidemiology</topic><topic>Child</topic><topic>Disease Outbreaks - prevention & control</topic><topic>Genetic divergence</topic><topic>Herd immunity</topic><topic>Humans</topic><topic>Immunization</topic><topic>Major</topic><topic>Neurovirulence</topic><topic>Poliomyelitis - epidemiology</topic><topic>Poliomyelitis - prevention & control</topic><topic>Poliovirus - genetics</topic><topic>Poliovirus Vaccine, Oral - adverse effects</topic><topic>Risk Factors</topic><topic>Serogroup</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gray, Elizabeth J</creatorcontrib><creatorcontrib>Cooper, Laura V</creatorcontrib><creatorcontrib>Bandyopadhyay, Ananda S</creatorcontrib><creatorcontrib>Blake, Isobel M</creatorcontrib><creatorcontrib>Grassly, Nicholas C</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gray, Elizabeth J</au><au>Cooper, Laura V</au><au>Bandyopadhyay, Ananda S</au><au>Blake, Isobel M</au><au>Grassly, Nicholas C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Origins and Risk Factors for Serotype-2 Vaccine-Derived Poliovirus Emergences in Africa During 2016–2019</atitle><jtitle>The Journal of infectious diseases</jtitle><addtitle>J Infect Dis</addtitle><date>2023-06-28</date><risdate>2023</risdate><volume>228</volume><issue>1</issue><spage>80</spage><epage>88</epage><pages>80-88</pages><issn>0022-1899</issn><issn>1537-6613</issn><eissn>1537-6613</eissn><abstract>Abstract
Serotype 2 oral poliovirus vaccine (OPV2) can revert to regain wild-type neurovirulence and spread to cause emergences of vaccine-derived poliovirus (VDPV2). After its global withdrawal from routine immunization in 2016, outbreak response use has created a cycle of VDPV2 emergences that threaten eradication. We implemented a hierarchical model based on VP1 region genetic divergence, time, and location to attribute emergences to campaigns and identify risk factors. We found that a 10 percentage point increase in population immunity in children younger than 5 years at the campaign time and location corresponds to a 18.0% decrease (95% credible interval [CrI], 6.3%–28%) in per-campaign relative risk, and that campaign size is associated with emergence risk (relative risk scaling with population size to a power of 0.80; 95% CrI, .50–1.10). Our results imply how Sabin OPV2 can be used alongside the genetically stable but supply-limited novel OPV2 (listed for emergency use in November 2020) to minimize emergence risk.
Outbreaks of vaccine-derived poliovirus from rare reversion of type-2 Sabin vaccine strain inhibit polio eradication efforts. We use a hierarchical model, incorporating VP1 region genetic divergence and population movement, to estimate outbreak origins and risk factors for vaccine campaigns.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>36630295</pmid><doi>10.1093/infdis/jiad004</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1899 |
ispartof | The Journal of infectious diseases, 2023-06, Vol.228 (1), p.80-88 |
issn | 0022-1899 1537-6613 1537-6613 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10304761 |
source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; Alma/SFX Local Collection |
subjects | Africa - epidemiology Child Disease Outbreaks - prevention & control Genetic divergence Herd immunity Humans Immunization Major Neurovirulence Poliomyelitis - epidemiology Poliomyelitis - prevention & control Poliovirus - genetics Poliovirus Vaccine, Oral - adverse effects Risk Factors Serogroup Vaccines |
title | The Origins and Risk Factors for Serotype-2 Vaccine-Derived Poliovirus Emergences in Africa During 2016–2019 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T08%3A10%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Origins%20and%20Risk%20Factors%20for%20Serotype-2%20Vaccine-Derived%20Poliovirus%20Emergences%20in%20Africa%20During%202016%E2%80%932019&rft.jtitle=The%20Journal%20of%20infectious%20diseases&rft.au=Gray,%20Elizabeth%20J&rft.date=2023-06-28&rft.volume=228&rft.issue=1&rft.spage=80&rft.epage=88&rft.pages=80-88&rft.issn=0022-1899&rft.eissn=1537-6613&rft_id=info:doi/10.1093/infdis/jiad004&rft_dat=%3Cproquest_pubme%3E3051851302%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3051851302&rft_id=info:pmid/36630295&rft_oup_id=10.1093/infdis/jiad004&rfr_iscdi=true |