Cargando…

Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine

A previous phase 3, randomized, multicenter study showed the immunogenicity of a primary vaccination of subjects aged 11 to 17 years with the quadrivalent meningococcal vaccine conjugated to tetanus toxoid (MenACWY-TT) or the quadrivalent meningococcal polysaccharide vaccine (MenACWY-PS). This exten...

Descripción completa

Detalles Bibliográficos
Autores principales: Quiambao, Beatriz, Peyrani, Paula, Li, Ping, Cutler, Mark W., Van Der Wielen, Marie, Perez, John L., Webber, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482828/
https://www.ncbi.nlm.nih.gov/pubmed/32401600
http://dx.doi.org/10.1080/21645515.2020.1744363
_version_ 1783580855327784960
author Quiambao, Beatriz
Peyrani, Paula
Li, Ping
Cutler, Mark W.
Van Der Wielen, Marie
Perez, John L.
Webber, Chris
author_facet Quiambao, Beatriz
Peyrani, Paula
Li, Ping
Cutler, Mark W.
Van Der Wielen, Marie
Perez, John L.
Webber, Chris
author_sort Quiambao, Beatriz
collection PubMed
description A previous phase 3, randomized, multicenter study showed the immunogenicity of a primary vaccination of subjects aged 11 to 17 years with the quadrivalent meningococcal vaccine conjugated to tetanus toxoid (MenACWY-TT) or the quadrivalent meningococcal polysaccharide vaccine (MenACWY-PS). This extension study evaluated the safety and immunogenicity of a MenACWY-TT booster 10 years after receiving a primary dose of either MenACWY-TT or MenACWY-PS. The primary immunogenicity endpoint was booster response, evaluated using serum bactericidal antibody assays with rabbit complement (rSBA), 1 month postbooster. Safety endpoints included the percentage of subjects experiencing local and general adverse events (AEs) ≤4 days after MenACWY-TT booster. Of 229 subjects enrolled, 169 and 58 in the MenACWY-TT and MenACWY-PS groups, respectively, completed the booster phase. The 1 month postbooster response for each serogroup ranged from 81.5% to 95.7% for MenACWY-TT and 66.7% to 94.1% for MenACWY-PS. Similar percentages of MenACWY-TT and MenACWY-PS recipients had a booster response to serogroups A, W, and Y, whereas more MenACWY-TT recipients than MenACWY-PS recipients had a booster response to serogroup C. For the MenACWY-TT and MenACWY-PS groups, respectively, the MenACWY-TT booster elicited rSBA titers ≥1:8 in 100% and ≥98.0% of subjects across all serogroups; 100% and ≥96.1% of all subjects had titers ≥1:128. No new safety signals were observed during the booster phase. In conclusion, a MenACWY-TT booster dose after receiving either a primary dose of MenACWY-TT or MenACWY-PS elicited robust immune responses and was well tolerated. Functional antibody responses last up to 10 years after primary MenACWY-TT vaccination.
format Online
Article
Text
id pubmed-7482828
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-74828282020-09-16 Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine Quiambao, Beatriz Peyrani, Paula Li, Ping Cutler, Mark W. Van Der Wielen, Marie Perez, John L. Webber, Chris Hum Vaccin Immunother Research Paper A previous phase 3, randomized, multicenter study showed the immunogenicity of a primary vaccination of subjects aged 11 to 17 years with the quadrivalent meningococcal vaccine conjugated to tetanus toxoid (MenACWY-TT) or the quadrivalent meningococcal polysaccharide vaccine (MenACWY-PS). This extension study evaluated the safety and immunogenicity of a MenACWY-TT booster 10 years after receiving a primary dose of either MenACWY-TT or MenACWY-PS. The primary immunogenicity endpoint was booster response, evaluated using serum bactericidal antibody assays with rabbit complement (rSBA), 1 month postbooster. Safety endpoints included the percentage of subjects experiencing local and general adverse events (AEs) ≤4 days after MenACWY-TT booster. Of 229 subjects enrolled, 169 and 58 in the MenACWY-TT and MenACWY-PS groups, respectively, completed the booster phase. The 1 month postbooster response for each serogroup ranged from 81.5% to 95.7% for MenACWY-TT and 66.7% to 94.1% for MenACWY-PS. Similar percentages of MenACWY-TT and MenACWY-PS recipients had a booster response to serogroups A, W, and Y, whereas more MenACWY-TT recipients than MenACWY-PS recipients had a booster response to serogroup C. For the MenACWY-TT and MenACWY-PS groups, respectively, the MenACWY-TT booster elicited rSBA titers ≥1:8 in 100% and ≥98.0% of subjects across all serogroups; 100% and ≥96.1% of all subjects had titers ≥1:128. No new safety signals were observed during the booster phase. In conclusion, a MenACWY-TT booster dose after receiving either a primary dose of MenACWY-TT or MenACWY-PS elicited robust immune responses and was well tolerated. Functional antibody responses last up to 10 years after primary MenACWY-TT vaccination. Taylor & Francis 2020-05-13 /pmc/articles/PMC7482828/ /pubmed/32401600 http://dx.doi.org/10.1080/21645515.2020.1744363 Text en © 2020 Pfizer, Inc. Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Research Paper
Quiambao, Beatriz
Peyrani, Paula
Li, Ping
Cutler, Mark W.
Van Der Wielen, Marie
Perez, John L.
Webber, Chris
Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine
title Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine
title_full Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine
title_fullStr Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine
title_full_unstemmed Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine
title_short Efficacy and safety of a booster dose of the meningococcal A, C, W, Y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine
title_sort efficacy and safety of a booster dose of the meningococcal a, c, w, y-tetanus toxoid conjugate vaccine administered 10 years after primary vaccination and long-term persistence of tetanus toxoid conjugate or polysaccharide vaccine
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7482828/
https://www.ncbi.nlm.nih.gov/pubmed/32401600
http://dx.doi.org/10.1080/21645515.2020.1744363
work_keys_str_mv AT quiambaobeatriz efficacyandsafetyofaboosterdoseofthemeningococcalacwytetanustoxoidconjugatevaccineadministered10yearsafterprimaryvaccinationandlongtermpersistenceoftetanustoxoidconjugateorpolysaccharidevaccine
AT peyranipaula efficacyandsafetyofaboosterdoseofthemeningococcalacwytetanustoxoidconjugatevaccineadministered10yearsafterprimaryvaccinationandlongtermpersistenceoftetanustoxoidconjugateorpolysaccharidevaccine
AT liping efficacyandsafetyofaboosterdoseofthemeningococcalacwytetanustoxoidconjugatevaccineadministered10yearsafterprimaryvaccinationandlongtermpersistenceoftetanustoxoidconjugateorpolysaccharidevaccine
AT cutlermarkw efficacyandsafetyofaboosterdoseofthemeningococcalacwytetanustoxoidconjugatevaccineadministered10yearsafterprimaryvaccinationandlongtermpersistenceoftetanustoxoidconjugateorpolysaccharidevaccine
AT vanderwielenmarie efficacyandsafetyofaboosterdoseofthemeningococcalacwytetanustoxoidconjugatevaccineadministered10yearsafterprimaryvaccinationandlongtermpersistenceoftetanustoxoidconjugateorpolysaccharidevaccine
AT perezjohnl efficacyandsafetyofaboosterdoseofthemeningococcalacwytetanustoxoidconjugatevaccineadministered10yearsafterprimaryvaccinationandlongtermpersistenceoftetanustoxoidconjugateorpolysaccharidevaccine
AT webberchris efficacyandsafetyofaboosterdoseofthemeningococcalacwytetanustoxoidconjugatevaccineadministered10yearsafterprimaryvaccinationandlongtermpersistenceoftetanustoxoidconjugateorpolysaccharidevaccine