Immunogenicity and safety of a 13-valent pneumococcal conjugate vaccine administered to older infants and children naive to pneumococcal vaccination

被引:18
作者
Wysocki, Jacek [1 ]
Brzostek, Jerzy [2 ]
Szymanski, Henryk [3 ]
Tetiurka, Boguslaw [4 ]
Toporowska-Kowalska, Ewa [5 ]
Wasowska-Krolikowska, Krystyna [5 ]
Sarkozy, Denise A. [6 ]
Giardina, Peter C. [7 ]
Gruber, William C. [7 ]
Emini, Emilio A. [7 ]
Scott, Daniel A. [7 ]
机构
[1] Poznan Univ Med Sci, Dept Prevent Med, PL-60179 Poznan, Poland
[2] NZOZ Debicy, Poradnia, Debica, Poland
[3] Rodzinnego Alina GrockaWlailak, NZOZ Praktyka Lekarza, Oborniki Slaskie, Poland
[4] NZOZ Salmed, Poradnia, Leczna, Poland
[5] Med Univ Lodz, Dept Paediat Allergol Gastroenterol & Nutr, Lodz, Poland
[6] Pfizer Inc, Collegeville, PA USA
[7] Pfizer Inc, Vaccine Clin Res, Pearl River, NY 10965 USA
关键词
Pneumococcal conjugate vaccine; Vaccine clinical evaluation; Immunization; Immunogenicity; HEALTHY INFANTS; SEROTYPES; DISEASE; SCHEDULE; TERM;
D O I
10.1016/j.vaccine.2015.02.005
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: Streptococcus pneumoniae infections are a major cause of morbidity and mortality in children <5 years old worldwide. To increase serotype coverage globally, a 13-valent pneumococcal conjugate vaccine (PCV13) has been developed and approved in many countries worldwide. Objective: Assess the safety and immunogenicity of PCV13 in healthy older infants and children naive to previous pneumococcal vaccination. Methods: This was a phase 3, open-label, multicenter study conducted in Polish children (N=354) who were vaccinated according to 3 age-appropriate catch-up schedules: Group 1 (aged 7 to <12 months) received two PCV13 doses with a booster at 12-16 months of age; Group 2 (aged 12 to <24 months) received two vaccine doses only; and Group 3 (aged 24 to <72 months) received a single dose of PCV13. Statistical analyses were descriptive. The proportion of immunological "responders" achieving serotype-specific antipneumococcal polysaccharide concentrations >= 0.35 mu g/mL, 1-month after the last dose of vaccine, was determined for each vaccine serotype. In addition, antipolysaccharide immunoglobulin (Ig) G geometric mean concentrations (GMCs) were calculated. Safety assessments included systemic and local reactions, and adverse events. Results: The proportion of immunological responders was >= 88% across groups for all serotypes. Antipolysaccharide IgG GMCs were generally similar across groups. Each schedule elicited immune response levels against all 13 serotypes comparable to or greater than levels previously reported in infants after a 3-dose series. The 3 catch-up schedules had similar tolerability and safety profiles; a trend was present towards greater local tenderness with increasing age and subsequent dose administration. Conclusions: Immunological responses and safety results support the use of PCV13 for catch-up schedules in older infants and children naive to pneumococcal vaccination. (C) 2015 Published by Elsevier Ltd.
引用
收藏
页码:1719 / 1725
页数:7
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