A phase III observer-blind randomized, controlled study to evaluate the immune response and the correlation with nasopharyngeal carriage after immunization of university students with a quadrivalent meningococcal ACWY glycoconjugate or serogroup B meningococcal vaccine

Abstract Background University students have high rates of pharyngeal carriage of Neisseria meningitidis . Interruption of carriage acquisition is an important mechanism of vaccines for inducing herd protection. 4CMenB and MenACWY-CRM vaccines have been shown to be immunogenic against meningococcal...

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Veröffentlicht in:Vaccine 2017-01, Vol.35 (3), p.427-434
Hauptverfasser: Read, Robert C, Dull, Peter, Bai, Xilian, Nolan, Kate, Findlow, Jamie, Bazaz, Rohit, Kleinschmidt, Annett, McCarthy, Maggie, Wang, Huajun, Toneatto, Daniela, Borrow, Ray
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container_end_page 434
container_issue 3
container_start_page 427
container_title Vaccine
container_volume 35
creator Read, Robert C
Dull, Peter
Bai, Xilian
Nolan, Kate
Findlow, Jamie
Bazaz, Rohit
Kleinschmidt, Annett
McCarthy, Maggie
Wang, Huajun
Toneatto, Daniela
Borrow, Ray
description Abstract Background University students have high rates of pharyngeal carriage of Neisseria meningitidis . Interruption of carriage acquisition is an important mechanism of vaccines for inducing herd protection. 4CMenB and MenACWY-CRM vaccines have been shown to be immunogenic against meningococcal serogroups B and ACWY respectively in younger age groups, and also to elicit a modest impact on meningococcal carriage in vaccinated students. However, vaccine responses in university students and the impact of serum bactericidal antibody (SBA) titers on meningococcal carriage are undetermined. Methods Immunogenicity of two 4CMenB doses or one MenACWY-CRM dose was measured in university students at Months 2, 4, 6 and 12 post-first vaccination. Immunogenicity of one MenACWY-CRM dose in students with previous meningococcal serogroup C conjugate vaccination was also assessed. Immune responses were measured with an SBA assay using human complement (hSBA) against three reference strains for serogroup B and against one strain for each for serogroups C and Y. Correlations between hSBA titers and meningococcal carriage were analyzed. Results All subjects demonstrated robust functional antibody responses to both vaccines at Month 2 and a high proportion maintained protective hSBA titers up to Month 12. At baseline, carriage of disease-associated serogroup B strains and serogroups C and Y were higher in subjects with already-protective hSBA titers. Post-vaccination, while both 4CMenB and MenACWY-CRM elicited robust immunogenicity in students, significant correlations between post-vaccination hSBA titers and carriage of disease-associated serogroups were not observed. Conclusions 4CMenB and MenACWY-CRM were both highly immunogenic. There was no correlation between carriage and post-vaccination hSBA titers.
doi_str_mv 10.1016/j.vaccine.2016.11.071
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Interruption of carriage acquisition is an important mechanism of vaccines for inducing herd protection. 4CMenB and MenACWY-CRM vaccines have been shown to be immunogenic against meningococcal serogroups B and ACWY respectively in younger age groups, and also to elicit a modest impact on meningococcal carriage in vaccinated students. However, vaccine responses in university students and the impact of serum bactericidal antibody (SBA) titers on meningococcal carriage are undetermined. Methods Immunogenicity of two 4CMenB doses or one MenACWY-CRM dose was measured in university students at Months 2, 4, 6 and 12 post-first vaccination. Immunogenicity of one MenACWY-CRM dose in students with previous meningococcal serogroup C conjugate vaccination was also assessed. Immune responses were measured with an SBA assay using human complement (hSBA) against three reference strains for serogroup B and against one strain for each for serogroups C and Y. Correlations between hSBA titers and meningococcal carriage were analyzed. Results All subjects demonstrated robust functional antibody responses to both vaccines at Month 2 and a high proportion maintained protective hSBA titers up to Month 12. At baseline, carriage of disease-associated serogroup B strains and serogroups C and Y were higher in subjects with already-protective hSBA titers. Post-vaccination, while both 4CMenB and MenACWY-CRM elicited robust immunogenicity in students, significant correlations between post-vaccination hSBA titers and carriage of disease-associated serogroups were not observed. Conclusions 4CMenB and MenACWY-CRM were both highly immunogenic. There was no correlation between carriage and post-vaccination hSBA titers.</description><identifier>ISSN: 0264-410X</identifier><identifier>EISSN: 1873-2518</identifier><identifier>DOI: 10.1016/j.vaccine.2016.11.071</identifier><identifier>PMID: 27912986</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adolescent ; Allergy and Immunology ; Antibodies, Bacterial - blood ; Blood Bactericidal Activity ; Carriage ; Carrier State - microbiology ; Carrier State - prevention &amp; control ; Female ; Humans ; Immune response ; Immunization ; Immunogenicity ; Male ; Meningococcal ; Meningococcal Infections - microbiology ; Meningococcal Infections - prevention &amp; control ; Meningococcal Vaccines - administration &amp; dosage ; Meningococcal Vaccines - immunology ; Nasopharynx - microbiology ; Neisseria meningitidis ; Neisseria meningitidis - classification ; Neisseria meningitidis - isolation &amp; purification ; Proteins ; Serogroup B ; Single-Blind Method ; Students ; Universities ; Vaccine ; Vaccines ; Young Adult</subject><ispartof>Vaccine, 2017-01, Vol.35 (3), p.427-434</ispartof><rights>2016</rights><rights>Copyright © 2016. Published by Elsevier Ltd.</rights><rights>Copyright Elsevier Limited Jan 11, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-c72152f09e904af32bea82984940454d9c8a78983cd4ae49cfe0c2eeb048831c3</citedby><cites>FETCH-LOGICAL-c528t-c72152f09e904af32bea82984940454d9c8a78983cd4ae49cfe0c2eeb048831c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1852985547?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,64361,64363,64365,65309,72215</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27912986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Read, Robert C</creatorcontrib><creatorcontrib>Dull, Peter</creatorcontrib><creatorcontrib>Bai, Xilian</creatorcontrib><creatorcontrib>Nolan, Kate</creatorcontrib><creatorcontrib>Findlow, Jamie</creatorcontrib><creatorcontrib>Bazaz, Rohit</creatorcontrib><creatorcontrib>Kleinschmidt, Annett</creatorcontrib><creatorcontrib>McCarthy, Maggie</creatorcontrib><creatorcontrib>Wang, Huajun</creatorcontrib><creatorcontrib>Toneatto, Daniela</creatorcontrib><creatorcontrib>Borrow, Ray</creatorcontrib><title>A phase III observer-blind randomized, controlled study to evaluate the immune response and the correlation with nasopharyngeal carriage after immunization of university students with a quadrivalent meningococcal ACWY glycoconjugate or serogroup B meningococcal vaccine</title><title>Vaccine</title><addtitle>Vaccine</addtitle><description>Abstract Background University students have high rates of pharyngeal carriage of Neisseria meningitidis . Interruption of carriage acquisition is an important mechanism of vaccines for inducing herd protection. 4CMenB and MenACWY-CRM vaccines have been shown to be immunogenic against meningococcal serogroups B and ACWY respectively in younger age groups, and also to elicit a modest impact on meningococcal carriage in vaccinated students. However, vaccine responses in university students and the impact of serum bactericidal antibody (SBA) titers on meningococcal carriage are undetermined. Methods Immunogenicity of two 4CMenB doses or one MenACWY-CRM dose was measured in university students at Months 2, 4, 6 and 12 post-first vaccination. Immunogenicity of one MenACWY-CRM dose in students with previous meningococcal serogroup C conjugate vaccination was also assessed. Immune responses were measured with an SBA assay using human complement (hSBA) against three reference strains for serogroup B and against one strain for each for serogroups C and Y. Correlations between hSBA titers and meningococcal carriage were analyzed. Results All subjects demonstrated robust functional antibody responses to both vaccines at Month 2 and a high proportion maintained protective hSBA titers up to Month 12. At baseline, carriage of disease-associated serogroup B strains and serogroups C and Y were higher in subjects with already-protective hSBA titers. Post-vaccination, while both 4CMenB and MenACWY-CRM elicited robust immunogenicity in students, significant correlations between post-vaccination hSBA titers and carriage of disease-associated serogroups were not observed. Conclusions 4CMenB and MenACWY-CRM were both highly immunogenic. 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Interruption of carriage acquisition is an important mechanism of vaccines for inducing herd protection. 4CMenB and MenACWY-CRM vaccines have been shown to be immunogenic against meningococcal serogroups B and ACWY respectively in younger age groups, and also to elicit a modest impact on meningococcal carriage in vaccinated students. However, vaccine responses in university students and the impact of serum bactericidal antibody (SBA) titers on meningococcal carriage are undetermined. Methods Immunogenicity of two 4CMenB doses or one MenACWY-CRM dose was measured in university students at Months 2, 4, 6 and 12 post-first vaccination. Immunogenicity of one MenACWY-CRM dose in students with previous meningococcal serogroup C conjugate vaccination was also assessed. Immune responses were measured with an SBA assay using human complement (hSBA) against three reference strains for serogroup B and against one strain for each for serogroups C and Y. Correlations between hSBA titers and meningococcal carriage were analyzed. Results All subjects demonstrated robust functional antibody responses to both vaccines at Month 2 and a high proportion maintained protective hSBA titers up to Month 12. At baseline, carriage of disease-associated serogroup B strains and serogroups C and Y were higher in subjects with already-protective hSBA titers. Post-vaccination, while both 4CMenB and MenACWY-CRM elicited robust immunogenicity in students, significant correlations between post-vaccination hSBA titers and carriage of disease-associated serogroups were not observed. Conclusions 4CMenB and MenACWY-CRM were both highly immunogenic. There was no correlation between carriage and post-vaccination hSBA titers.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>27912986</pmid><doi>10.1016/j.vaccine.2016.11.071</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Elsevier ScienceDirect Journals; ProQuest Central UK/Ireland
subjects Adolescent
Allergy and Immunology
Antibodies, Bacterial - blood
Blood Bactericidal Activity
Carriage
Carrier State - microbiology
Carrier State - prevention & control
Female
Humans
Immune response
Immunization
Immunogenicity
Male
Meningococcal
Meningococcal Infections - microbiology
Meningococcal Infections - prevention & control
Meningococcal Vaccines - administration & dosage
Meningococcal Vaccines - immunology
Nasopharynx - microbiology
Neisseria meningitidis
Neisseria meningitidis - classification
Neisseria meningitidis - isolation & purification
Proteins
Serogroup B
Single-Blind Method
Students
Universities
Vaccine
Vaccines
Young Adult
title A phase III observer-blind randomized, controlled study to evaluate the immune response and the correlation with nasopharyngeal carriage after immunization of university students with a quadrivalent meningococcal ACWY glycoconjugate or serogroup B meningococcal vaccine
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