Professor, Department of Pediatrics, Kawasaki Medical School, Japan.
Mitsubishi Tanabe Pharma Corporation, Japan.
Vaccine. 2024 Apr 30;42(12):3134-3143. doi: 10.1016/j.vaccine.2023.03.077. Epub 2024 Apr 6.
This study investigated the immunogenicity and safety of a pentavalent vaccine Gobik (DPT-IPV-Haemophilus influenzae type b [Hib]) in healthy Japanese infants aged ≥ 2 and < 43 months using a concomitant vaccination with ActHIB® (Hib) and Tetrabik (DPT-IPV) as a comparator.
This study was conducted as a phase 3, multicenter, active controlled, assessor-blinded, randomized, parallel-group study. Participants received a total of 4 subcutaneous doses (3 primary immunization doses and a booster dose) of either the experimental drug (DPT-IPV-Hib) or the active comparator (Hib + DPT-IPV). The primary endpoints were the anti-PRP antibody prevalence rate with ≥ 1 μg/mL, and the antibody prevalence rates against pertussis, diphtheria toxin, tetanus toxin, and attenuated poliovirus after the primary immunization.
In 267 randomized participants (133 in the DPT-IPV-Hib group and 134 in the Hib + DPT-IPV group), the antibody prevalence rates after the primary immunization in both groups were 100.0 % and 88.7 % for anti-PRP antibody with ≥ 1 μg/mL, 99.2 % and 98.5 % against diphtheria toxin, and 100.0 % and 99.2 % against tetanus toxin, respectively. The antibody prevalence rates against pertussis and attenuated poliovirus were 100.0 % in both groups. The non-inferiority of the DPT-IPV-Hib group to the Hib + DPT-IPV group was verified for all measured antibodies. In both groups, all the GMTs of antibodies after the primary immunization were higher than those before the first dose, and those after the booster dose were higher than those after the primary immunization. No safety issues were identified.
A single-agent Gobik, the first DPT-IPV-Hib pentavalent vaccine approved in Japan, was confirmed to simultaneously provide primary and booster immunizations against Hib infection, pertussis, diphtheria, tetanus, and poliomyelitis and to have a preventive effect and safety comparable to concomitant vaccination with Hib (ActHIB®) and DPT-IPV quadrivalent vaccine (Tetrabik).
本研究旨在通过与 ActHIB®(Hib)和 Tetrabik(DPT-IPV)同时接种作为对照,评估 2 岁至 43 个月龄健康日本婴儿中五价疫苗 Gobik(DPT-IPV-Haemophilus influenzae type b [Hib])的免疫原性和安全性。
这是一项 3 期、多中心、活性对照、评估者盲法、随机、平行组研究。参与者共接受 4 次皮下剂量(3 次基础免疫剂量和 1 次加强免疫剂量)的试验药物(DPT-IPV-Hib)或活性对照(Hib+DPT-IPV)。主要终点是抗 PRP 抗体阳性率≥1μg/mL,以及基础免疫后百日咳、白喉毒素、破伤风毒素和减毒脊髓灰质炎病毒的抗体阳性率。
在 267 名随机参与者(DPT-IPV-Hib 组 133 名,Hib+DPT-IPV 组 134 名)中,两组基础免疫后抗 PRP 抗体阳性率均为 100.0%和 88.7%(抗 PRP 抗体≥1μg/mL),白喉毒素分别为 99.2%和 98.5%,破伤风毒素分别为 100.0%和 99.2%。两组百日咳和减毒脊髓灰质炎病毒的抗体阳性率均为 100.0%。DPT-IPV-Hib 组与 Hib+DPT-IPV 组相比,所有抗体均具有非劣效性。两组基础免疫后抗体 GMT 均高于首剂,加强免疫后高于基础免疫。未发现安全性问题。
日本批准的首个 DPT-IPV-Hib 五价疫苗 Gobik 可同时提供 Hib 感染、百日咳、白喉、破伤风和脊髓灰质炎的基础和加强免疫,预防效果和安全性与 Hib(ActHIB®)和 DPT-IPV 四价疫苗(Tetrabik)同时接种相当。