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在日本健康婴幼儿中进行基础免疫和加强免疫接种的白百破-灭活脊髓灰质炎疫苗/ b型流感嗜血杆菌结合疫苗五价疫苗的免疫原性和安全性

Immunogenicity and safety of a DTaP-IPV/Hib pentavalent vaccine given as primary and booster vaccinations in healthy infants and toddlers in Japan.

作者信息

Nakayama Tetsuo, Vidor Emmanuel, Tsuzuki Daisuke, Nishina Satoshi, Sasaki Toru, Ishii Yasunori, Mizukami Hideya, Tsuge Hiroyuki

机构信息

Kitasato Institute for Life Sciences, Tokyo, Japan.

Sanofi Pasteur, Lyon, France.

出版信息

J Infect Chemother. 2020 Jul;26(7):651-659. doi: 10.1016/j.jiac.2019.11.012. Epub 2020 Apr 16.

Abstract

BACKGROUND

Globally, the use of single DTaP-IPV/Hib vaccines that combine DTaP-IPV and Hib is widespread, but in Japan vaccination is usually concomitant at separate sites. The immunogenicity and safety of a primary vaccination series and booster of a combined pentavalent DTaP-IPV/Hib vaccine were evaluated and compared to separate administration of DTaP-IPV and Hib in Japanese infants.

METHODS

Healthy Japanese infants were administered DTaP-IPV/Hib (Group A: N = 207) or DTaP-IPV + Hib (Group B: N = 207) by the subcutaneous (SC) or DTaP-IPV/Hib by the intramuscular (IM) route (Group C: N = 10). All subjects received a 3-dose primary vaccination series and a booster. Non-inferiority (Group A versus Group B) was tested post-primary series and subsequent post hoc analyses were performed for anti-Hib. Safety was assessed by parental reports.

RESULTS

Non-inferiority for SC administration of Group A versus Group B for the primary series was demonstrated for antibody responses to all antigens except Hib using the threshold of 1.0 μg/mL. Post hoc analyses for anti-Hib demonstrated non-inferiority for the primary series response using 0.15 μg/mL, and for pre-booster antibody persistence and the booster response using 0.15 μg/mL and 1.0 μg/mL. The immune response was similar for each antigen following SC or IM administration. There were no safety concerns in any group, and a lower incidence of injection sites for the IM route was observed as expected.

CONCLUSIONS

These data show the good immunogenicity and safety profile of the DTaP-IPV/Hib vaccine as a 3-dose infant primary series followed by a booster in the second year of life in Japan.

摘要

背景

在全球范围内,同时包含白喉、破伤风、无细胞百日咳、灭活脊髓灰质炎病毒和B型流感嗜血杆菌(DTaP-IPV/Hib)的单一疫苗使用广泛,但在日本,疫苗接种通常在不同部位同时进行。本研究评估了五价DTaP-IPV/Hib联合疫苗初次免疫系列和加强免疫的免疫原性及安全性,并与日本婴儿分别接种DTaP-IPV和Hib疫苗的情况进行比较。

方法

健康日本婴儿分别接受皮下注射(SC)DTaP-IPV/Hib(A组:N = 207)或DTaP-IPV + Hib(B组:N = 207),或肌肉注射(IM)DTaP-IPV/Hib(C组:N = 10)。所有受试者均接受3剂次的初次免疫系列和1剂次加强免疫。在初次免疫系列后测试A组与B组的非劣效性,并对B型流感嗜血杆菌抗体进行事后分析。通过家长报告评估安全性。

结果

A组与B组初次免疫系列皮下注射的非劣效性在除B型流感嗜血杆菌外的所有抗原抗体反应中得到证实,阈值为1.0μg/mL。B型流感嗜血杆菌抗体的事后分析表明,初次免疫系列反应在阈值为0.15μg/mL时具有非劣效性,加强免疫前抗体持久性和加强免疫反应在阈值分别为0.15μg/mL和1.0μg/mL时具有非劣效性。皮下注射或肌肉注射后各抗原的免疫反应相似。任何组均无安全性问题,且如预期的那样,肌肉注射途径的注射部位发生率较低。

结论

这些数据表明,在日本,DTaP-IPV/Hib疫苗作为3剂次婴儿初次免疫系列并在出生后第二年进行加强免疫,具有良好的免疫原性和安全性。

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