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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.
Afiliación
  • Quiambao B; Clinical Research Division, Research Institute for Tropical Medicine , Alabang, Muntinlupa City, Philippines.
  • Peyrani P; Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Collegeville, PA, USA.
  • Li P; Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Collegeville, PA, USA.
  • Cutler MW; Pfizer Vaccine Research and Development, Pfizer Inc , Pearl River, NY, USA.
  • Van Der Wielen M; Vaccines R & D, GlaxoSmithKline , Wavre, Belgium.
  • Perez JL; Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Collegeville, PA, USA.
  • Webber C; Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Hurley, UK.
Hum Vaccin Immunother ; 16(6): 1272-1279, 2020 06 02.
Article en En | MEDLINE | ID: mdl-32401600
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vacunas Meningococicas / Infecciones Meningocócicas Límite: Humans Idioma: En Revista: Hum Vaccin Immunother Año: 2020 Tipo del documento: Article País de afiliación: Filipinas

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vacunas Meningococicas / Infecciones Meningocócicas Límite: Humans Idioma: En Revista: Hum Vaccin Immunother Año: 2020 Tipo del documento: Article País de afiliación: Filipinas