Nakayama Tetsuo, Vidor Emmanuel, Tsuzuki Daisuke, Nishina Satoshi, Sasaki Toru, Ishii Yasunori, Mizukami Hideya, Tsuge Hiroyuki
Kitasato Institute for Life Sciences, Tokyo, Japan.
Sanofi Pasteur, Lyon, France.
J Infect Chemother. 2020 Jul;26(7):651-659. doi: 10.1016/j.jiac.2019.11.012. Epub 2020 Apr 16.
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.
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.
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.
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.
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。
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。
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。
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。