Immunogenicity and Safety of a Booster Dose of the 10-valent Pneumococcal Haemophilus Influenzae Protein D Conjugate Vaccine Coadministered With the Tetravalent Meningococcal Serogroups A, C, W-135 and Y Tetanus Toxoid Conjugate Vaccine in Toddlers: A Randomized Trial

被引:17
|
作者
Ruiz-Palacios, Guillermo M. [2 ]
Huang, Li-Min [3 ]
Lin, Tzou-Yien [4 ]
Hernandez, Lorena [5 ]
Guerrero, M. Lourdes [2 ]
Villalobos, Antonio Lavalle [5 ]
Van der Wielen, Marie [1 ]
Moreira, Marta
Fissette, Laurence
Borys, Dorota
Miller, Jacqueline M. [6 ]
机构
[1] GlaxoSmithKline Vaccines, Global Vaccine Clin Dev, Neisseria Vaccines, B-1300 Wavre, Belgium
[2] Inst Nacl Ciencias Med & Nutr Salvador Zubiran, Mexico City, DF, Mexico
[3] Natl Taiwan Univ Hosp, Taipei, Taiwan
[4] Chang Gung Univ, Coll Med, Chang Gung Childrens Hosp, Tao Yuan, Taiwan
[5] Hosp Gen Dr Manuel Gea Gonzalez, Mexico City, DF, Mexico
[6] GlaxoSmithKline Vaccines, Global Vaccine Clin Dev, King Of Prussia, PA USA
关键词
Streptococcus pneumoniae; Neisseria meningitidis; coadministration; conjugate vaccines; toddlers; NEISSERIA-MENINGITIDIS SEROGROUP; RUBELLA-VARICELLA VACCINE; PHID-CV; STREPTOCOCCUS-PNEUMONIAE; CHILDHOOD VACCINES; DTPW-HBV/HIB; REACTOGENICITY; STANDARDIZATION; ADOLESCENTS; EFFICACY;
D O I
10.1097/INF.0b013e3182784143
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: This open, randomized clinical trial (NCT00758264) evaluated the coadministration of a booster dose of the 10-valent pneumococcal conjugate vaccine (PHiD-CV) and a single dose of the tetravalent meningococcal conjugate vaccine (MenACWY-TT) in Taiwanese and Mexican toddlers. Methods: Healthy toddlers aged 12-23 months (N = 363) were randomized (2:1:1) to receive either both vaccines at first visit, MenACWY-TT at first visit and 1 month later PHiD-CV, or PHiD-CV at first visit and 1 month later MenACWY-TT. Immune responses were measured 1 month after MenACWY-TT vaccination by meningococcal serum bactericidal activity (rSBA) assay and 1 month after PHiD-CV vaccination by pneumococcal 22F-inhibition enzyme-linked immunosorbent assay and functional opsonophagocytic activity assay. Solicited and unsolicited symptoms were recorded for days 4 and 31 postvaccination, respectively. Serious adverse events were recorded throughout the study. Results: The prespecified criteria for noninferiority of coadministration versus individual administrations were met for all meningococcal serogroups (in terms of percentages of toddlers with rSBA titer >= 8) and all vaccine pneumococcal serotypes (in terms of antibody geometric mean concentration ratios), except pneumococcal serotype 18C. For each meningococcal serogroup, >= 97.5% of toddlers across the 3 groups had rSBA titers >= 128 at 1 month after MenACWY-TT vaccination. For each pneumococcal serotype, at 1 month after PHiD-CV vaccination, >= 96.0% and >= 92.9% of toddlers across the 3 groups had antibody concentrations >= 0.2 mu g/mL and opsonophagocytic activity titers >= 8, respectively. The safety profiles of both vaccines when coadministered were clinically acceptable. Conclusions: This study supports the coadministration of PHiD-CV and MenACWY-TT in toddlers.
引用
收藏
页码:62 / 71
页数:10
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