Effectiveness of pertussis vaccination and duration of immunity
A resurgence of pertussis cases among both vaccinated and unvaccinated people raises questions about vaccine effectiveness over time. Our objective was to study the effectiveness of the pertussis vaccine and characterize the effect of waning immunity and whole-cell vaccine priming. We used the test-...
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Veröffentlicht in: | Canadian Medical Association journal (CMAJ) 2016-11, Vol.188 (16), p.E399-E406 |
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creator | Schwartz, Kevin L Kwong, Jeffrey C Deeks, Shelley L Campitelli, Michael A Jamieson, Frances B Marchand-Austin, Alex Stukel, Therese A Rosella, Laura Daneman, Nick Bolotin, Shelly Drews, Steven J Rilkoff, Heather Crowcroft, Natasha S |
description | A resurgence of pertussis cases among both vaccinated and unvaccinated people raises questions about vaccine effectiveness over time. Our objective was to study the effectiveness of the pertussis vaccine and characterize the effect of waning immunity and whole-cell vaccine priming.
We used the test-negative design, a nested case-control study with test-negative individuals as controls. We constructed multivariable logistic regression models to estimate odds ratios (ORs). Vaccine effectiveness was calculated as (1 - OR) × 100. We assessed waning immunity by calculating the odds of developing pertussis per year since last vaccination and evaluated the relative effectiveness of priming with acellular versus whole-cell vaccine.
Between Dec. 7, 2009, and Mar. 31, 2013, data on 5867 individuals (486 test-positive cases and 5381 test-negative controls) were available for analysis. Adjusted vaccine effectiveness was 80% (95% confidence interval [CI] 71% to 86%) at 15-364 days, 84% (95% CI 77% to 89%) at 1-3 years, 62% (95% CI 42% to 75%) at 4-7 years and 41% (95% CI 0% to 66%) at 8 or more years since last vaccination. We observed waning immunity with the acellular vaccine, with an adjusted OR for pertussis infection of 1.27 (95% CI 1.20 to 1.34) per year since last vaccination. Acellular, versus whole-cell, vaccine priming was associated with an increased odds of pertussis (adjusted OR 2.15, 95% CI 1.30 to 3.57).
We observed high early effectiveness of the pertussis vaccine that rapidly declined as time since last vaccination surpassed 4 years, particularly with acellular vaccine priming. Considering whole-cell vaccine priming and/or boosters in pregnancy to optimize pertussis control may be prudent. |
doi_str_mv | 10.1503/cmaj.160193 |
format | Article |
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We used the test-negative design, a nested case-control study with test-negative individuals as controls. We constructed multivariable logistic regression models to estimate odds ratios (ORs). Vaccine effectiveness was calculated as (1 - OR) × 100. We assessed waning immunity by calculating the odds of developing pertussis per year since last vaccination and evaluated the relative effectiveness of priming with acellular versus whole-cell vaccine.
Between Dec. 7, 2009, and Mar. 31, 2013, data on 5867 individuals (486 test-positive cases and 5381 test-negative controls) were available for analysis. Adjusted vaccine effectiveness was 80% (95% confidence interval [CI] 71% to 86%) at 15-364 days, 84% (95% CI 77% to 89%) at 1-3 years, 62% (95% CI 42% to 75%) at 4-7 years and 41% (95% CI 0% to 66%) at 8 or more years since last vaccination. We observed waning immunity with the acellular vaccine, with an adjusted OR for pertussis infection of 1.27 (95% CI 1.20 to 1.34) per year since last vaccination. Acellular, versus whole-cell, vaccine priming was associated with an increased odds of pertussis (adjusted OR 2.15, 95% CI 1.30 to 3.57).
We observed high early effectiveness of the pertussis vaccine that rapidly declined as time since last vaccination surpassed 4 years, particularly with acellular vaccine priming. Considering whole-cell vaccine priming and/or boosters in pregnancy to optimize pertussis control may be prudent.</description><identifier>ISSN: 0820-3946</identifier><identifier>EISSN: 1488-2329</identifier><identifier>DOI: 10.1503/cmaj.160193</identifier><identifier>PMID: 27672225</identifier><identifier>CODEN: CMAJAX</identifier><language>eng</language><publisher>Canada: Joule Inc</publisher><subject>Adolescent ; Age ; Ambulatory care ; Case-Control Studies ; Child ; Child, Preschool ; Disease Outbreaks - prevention & control ; Female ; Health care policy ; Humans ; Immune response ; Immunity, Active ; Immunization Schedule ; Incidence ; Infant ; Influenza ; Laboratories ; Logistic Models ; Male ; Mortality ; Multivariate Analysis ; Odds Ratio ; Ontario - epidemiology ; Pertussis Vaccine - therapeutic use ; Polymerase chain reaction ; Population ; Prevention ; Public health ; Sensitivity analysis ; Systematic review ; Teenagers ; Testing ; Vaccines ; Whooping cough ; Whooping Cough - epidemiology ; Whooping Cough - prevention & control ; Young Adult</subject><ispartof>Canadian Medical Association journal (CMAJ), 2016-11, Vol.188 (16), p.E399-E406</ispartof><rights>2016 Canadian Medical Association or its licensors.</rights><rights>COPYRIGHT 2016 Joule Inc.</rights><rights>Copyright 8872147 Canada Inc. Nov 1, 2016</rights><rights>2016 Joule Inc. or its licensors 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c710t-489ece6ba6e81cbb2b2292354e4d996348fcd57affa56d50198d48eac9e4bf233</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088088/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5088088/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27672225$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schwartz, Kevin L</creatorcontrib><creatorcontrib>Kwong, Jeffrey C</creatorcontrib><creatorcontrib>Deeks, Shelley L</creatorcontrib><creatorcontrib>Campitelli, Michael A</creatorcontrib><creatorcontrib>Jamieson, Frances B</creatorcontrib><creatorcontrib>Marchand-Austin, Alex</creatorcontrib><creatorcontrib>Stukel, Therese A</creatorcontrib><creatorcontrib>Rosella, Laura</creatorcontrib><creatorcontrib>Daneman, Nick</creatorcontrib><creatorcontrib>Bolotin, Shelly</creatorcontrib><creatorcontrib>Drews, Steven J</creatorcontrib><creatorcontrib>Rilkoff, Heather</creatorcontrib><creatorcontrib>Crowcroft, Natasha S</creatorcontrib><title>Effectiveness of pertussis vaccination and duration of immunity</title><title>Canadian Medical Association journal (CMAJ)</title><addtitle>CMAJ</addtitle><description>A resurgence of pertussis cases among both vaccinated and unvaccinated people raises questions about vaccine effectiveness over time. Our objective was to study the effectiveness of the pertussis vaccine and characterize the effect of waning immunity and whole-cell vaccine priming.
We used the test-negative design, a nested case-control study with test-negative individuals as controls. We constructed multivariable logistic regression models to estimate odds ratios (ORs). Vaccine effectiveness was calculated as (1 - OR) × 100. We assessed waning immunity by calculating the odds of developing pertussis per year since last vaccination and evaluated the relative effectiveness of priming with acellular versus whole-cell vaccine.
Between Dec. 7, 2009, and Mar. 31, 2013, data on 5867 individuals (486 test-positive cases and 5381 test-negative controls) were available for analysis. Adjusted vaccine effectiveness was 80% (95% confidence interval [CI] 71% to 86%) at 15-364 days, 84% (95% CI 77% to 89%) at 1-3 years, 62% (95% CI 42% to 75%) at 4-7 years and 41% (95% CI 0% to 66%) at 8 or more years since last vaccination. We observed waning immunity with the acellular vaccine, with an adjusted OR for pertussis infection of 1.27 (95% CI 1.20 to 1.34) per year since last vaccination. Acellular, versus whole-cell, vaccine priming was associated with an increased odds of pertussis (adjusted OR 2.15, 95% CI 1.30 to 3.57).
We observed high early effectiveness of the pertussis vaccine that rapidly declined as time since last vaccination surpassed 4 years, particularly with acellular vaccine priming. Considering whole-cell vaccine priming and/or boosters in pregnancy to optimize pertussis control may be prudent.</description><subject>Adolescent</subject><subject>Age</subject><subject>Ambulatory care</subject><subject>Case-Control Studies</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Disease Outbreaks - prevention & control</subject><subject>Female</subject><subject>Health care policy</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunity, Active</subject><subject>Immunization Schedule</subject><subject>Incidence</subject><subject>Infant</subject><subject>Influenza</subject><subject>Laboratories</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Mortality</subject><subject>Multivariate Analysis</subject><subject>Odds Ratio</subject><subject>Ontario - epidemiology</subject><subject>Pertussis Vaccine - therapeutic use</subject><subject>Polymerase chain reaction</subject><subject>Population</subject><subject>Prevention</subject><subject>Public health</subject><subject>Sensitivity analysis</subject><subject>Systematic review</subject><subject>Teenagers</subject><subject>Testing</subject><subject>Vaccines</subject><subject>Whooping cough</subject><subject>Whooping Cough - 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prevention & control</topic><topic>Female</topic><topic>Health care policy</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunity, Active</topic><topic>Immunization Schedule</topic><topic>Incidence</topic><topic>Infant</topic><topic>Influenza</topic><topic>Laboratories</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Mortality</topic><topic>Multivariate Analysis</topic><topic>Odds Ratio</topic><topic>Ontario - epidemiology</topic><topic>Pertussis Vaccine - therapeutic use</topic><topic>Polymerase chain reaction</topic><topic>Population</topic><topic>Prevention</topic><topic>Public health</topic><topic>Sensitivity analysis</topic><topic>Systematic review</topic><topic>Teenagers</topic><topic>Testing</topic><topic>Vaccines</topic><topic>Whooping cough</topic><topic>Whooping Cough - epidemiology</topic><topic>Whooping Cough - prevention & control</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwartz, Kevin L</creatorcontrib><creatorcontrib>Kwong, Jeffrey C</creatorcontrib><creatorcontrib>Deeks, Shelley L</creatorcontrib><creatorcontrib>Campitelli, Michael A</creatorcontrib><creatorcontrib>Jamieson, Frances B</creatorcontrib><creatorcontrib>Marchand-Austin, Alex</creatorcontrib><creatorcontrib>Stukel, Therese A</creatorcontrib><creatorcontrib>Rosella, Laura</creatorcontrib><creatorcontrib>Daneman, Nick</creatorcontrib><creatorcontrib>Bolotin, Shelly</creatorcontrib><creatorcontrib>Drews, Steven J</creatorcontrib><creatorcontrib>Rilkoff, Heather</creatorcontrib><creatorcontrib>Crowcroft, Natasha S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business & Current Affairs Database</collection><collection>Canadian Business & Current Affairs Database (Alumni Edition)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>British Nursing Index</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>British Nursing Index</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>CBCA Reference & Current Events</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Canadian Medical Association journal (CMAJ)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwartz, Kevin L</au><au>Kwong, Jeffrey C</au><au>Deeks, Shelley L</au><au>Campitelli, Michael A</au><au>Jamieson, Frances B</au><au>Marchand-Austin, Alex</au><au>Stukel, Therese A</au><au>Rosella, Laura</au><au>Daneman, Nick</au><au>Bolotin, Shelly</au><au>Drews, Steven J</au><au>Rilkoff, Heather</au><au>Crowcroft, Natasha S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effectiveness of pertussis vaccination and duration of immunity</atitle><jtitle>Canadian Medical Association journal (CMAJ)</jtitle><addtitle>CMAJ</addtitle><date>2016-11-01</date><risdate>2016</risdate><volume>188</volume><issue>16</issue><spage>E399</spage><epage>E406</epage><pages>E399-E406</pages><issn>0820-3946</issn><eissn>1488-2329</eissn><coden>CMAJAX</coden><abstract>A resurgence of pertussis cases among both vaccinated and unvaccinated people raises questions about vaccine effectiveness over time. Our objective was to study the effectiveness of the pertussis vaccine and characterize the effect of waning immunity and whole-cell vaccine priming.
We used the test-negative design, a nested case-control study with test-negative individuals as controls. We constructed multivariable logistic regression models to estimate odds ratios (ORs). Vaccine effectiveness was calculated as (1 - OR) × 100. We assessed waning immunity by calculating the odds of developing pertussis per year since last vaccination and evaluated the relative effectiveness of priming with acellular versus whole-cell vaccine.
Between Dec. 7, 2009, and Mar. 31, 2013, data on 5867 individuals (486 test-positive cases and 5381 test-negative controls) were available for analysis. Adjusted vaccine effectiveness was 80% (95% confidence interval [CI] 71% to 86%) at 15-364 days, 84% (95% CI 77% to 89%) at 1-3 years, 62% (95% CI 42% to 75%) at 4-7 years and 41% (95% CI 0% to 66%) at 8 or more years since last vaccination. We observed waning immunity with the acellular vaccine, with an adjusted OR for pertussis infection of 1.27 (95% CI 1.20 to 1.34) per year since last vaccination. Acellular, versus whole-cell, vaccine priming was associated with an increased odds of pertussis (adjusted OR 2.15, 95% CI 1.30 to 3.57).
We observed high early effectiveness of the pertussis vaccine that rapidly declined as time since last vaccination surpassed 4 years, particularly with acellular vaccine priming. Considering whole-cell vaccine priming and/or boosters in pregnancy to optimize pertussis control may be prudent.</abstract><cop>Canada</cop><pub>Joule Inc</pub><pmid>27672225</pmid><doi>10.1503/cmaj.160193</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Age Ambulatory care Case-Control Studies Child Child, Preschool Disease Outbreaks - prevention & control Female Health care policy Humans Immune response Immunity, Active Immunization Schedule Incidence Infant Influenza Laboratories Logistic Models Male Mortality Multivariate Analysis Odds Ratio Ontario - epidemiology Pertussis Vaccine - therapeutic use Polymerase chain reaction Population Prevention Public health Sensitivity analysis Systematic review Teenagers Testing Vaccines Whooping cough Whooping Cough - epidemiology Whooping Cough - prevention & control Young Adult |
title | Effectiveness of pertussis vaccination and duration of immunity |
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