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Evaluation of a Hexavalent-Pentavalent-Hexavalent Infant Primary Vaccination Series Followed by a Pentavalent Booster Vaccine in Healthy Infants and Toddlers

机译:评价六价五价 - 六价婴儿初级疫苗接种系列,其次是健康婴儿和幼儿的五价增压疫苗

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Background: This study assessed a pediatric mixed hexavalent diphtheria (D)-tetanus (T)-acellular pertussis (aP)-inactivated poliovirus (IPV)-hepatitis B (HB)-Haemophilus influenzae b [polyribosylribitol phosphate (PRP-T)]-pentavalent (DTaP-IPV//PRP-T)-hexavalent primary series schedule followed by a pentavalent booster. Methods: Healthy infants (N = 265) who had received a prior HB vaccination received a fully liquid, hexavalent vaccine (DTaP-IPV-HB-PRP-T) at 2 and 6 months of age and a reconstituted pentavalent vaccine (DTaP-IPV//PRP-T) at 4 months of age. Coadministered vaccines were pneumococcal vaccine at 2 and 4 months (and optionally at 6 months of age), rotavirus vaccine at 2, 4, 6 months and meningococcal serogroup C vaccine at 2 months. At 18 months, participants received DTaP-IPV//PRP-T and pneumococcal vaccine boosters. Immunogenicity was assessed using validated assays and safety by parental reports. Results: For the hexavalent and pentavalent vaccines, the primary series and booster immune responses in terms of seroprotection and vaccine response rates were high for all antigens (generally 99% and 95% for the primary series and booster, respectively) and prebooster antibody persistence was good for all antigens (in particular, 92.4% of participants had prebooster anti-HB antibody = 10 mIU/mL). The incidence of solicited reactions was lower after the booster vaccination (56.9%-73.1%) than the primary series (76.6%-97.4%); there were few vaccine-related unsolicited adverse events (1.9% and 1.5% for the primary series and booster, respectively), none led to participant discontinuation and none was serious. Conclusions: This study provides data that allow recommending authorities to consider the use of a sequential hexavalent-pentavalent-hexavalent primary vaccination series followed by a pentavalent booster in coadministration with other common childhood vaccines.
机译:背景:该研究评估了儿科混合六价赤肿(d) - 季节(t) - 术治疗(AP) - 活性脊髓灰质炎(IPV)-hopatisb(Hb)-Haemophilus甲酰胺(Polyribosylribitol磷酸盐(PrP-T)] - PentAvalent(DTAP-IPV // PRP-T) - 横向主要系列计划,然后是PentAvalent Booster。方法:接受先前Hb疫苗接种的健康婴儿(n = 265)在2和6个月的年龄和重构五价疫苗(DTAP-IPV // prp-t)在4个月的年龄。共同疫苗的疫苗在2和4个月(和6个月的6个月),2,4,6个月和脑膜炎球菌血清血群C疫苗2个月的肺炎球菌疫苗是2和4个月的疫苗。在18个月,参与者接受了DTAP-IPV // PRP-T和肺炎球菌疫苗助推器。使用父母报告使用验证的测定和安全性评估免疫原性。结果:对于六价化和五价疫苗,所有抗原的初级系列和疫苗反应率方面的初级系列和增强免疫应答(通常为初级系列和助推器99%和 95%)和预泊斯康斯特抗体持续性对于所有抗原(特别是,92.4%的参与者患者抗HB抗体> = 10 mIU / mL)。溶胶疫苗接种后征集反应的发病率降低(56.9%-73.1%)比初级系列(76.6%-97.4%);疫苗相关的未经请求不全的不良事件(分别为1.9%和1.5%,分别为1.9%和1.5%),没有导致参与者停产,没有严重。结论:本研究提供了允许推荐当局考虑使用顺序六价五价六价疫苗接种系列的数据,然后在与其他常见的儿童疫苗共同分配中的五价助推器。

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