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健康韩国婴儿中三联 DTPa-IPV/Hib 疫苗作为三剂基础免疫接种程序的免疫原性和安全性:III 期、随机研究。

Immunogenicity and safety of a combined DTPa-IPV/Hib vaccine administered as a three-dose primary vaccination course in healthy Korean infants: phase III, randomized study.

机构信息

a Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea Incheon, The Republic of Korea.

b Keimyung University School of Medicine , Daegu , The Republic of Korea.

出版信息

Hum Vaccin Immunother. 2019;15(2):317-326. doi: 10.1080/21645515.2018.1536588. Epub 2018 Nov 15.

Abstract

We assessed the immunogenicity and safety of a three-dose primary vaccination schedule with the combined diphtheria-tetanus-acellular pertussis-inactivated poliovirus/Haemophilus influenzae type b vaccine (DTPa-IPV/Hib) in Korean infants. In this phase III open-label, multicenter study (NCT01309646), healthy infants aged 42-69 days (randomized 1:1) received three doses of either pentavalent DTPa-IPV/Hib (DTPa-IPV/Hib group) or DTPa-IPV and Hib vaccines administered separately (DTPa-IPV+Hib group) at 2, 4, 6 months of age. The primary objective was to demonstrate non-inferiority of DTPa-IPV/Hib compared to DTPa-IPV+Hib vaccines in terms of immune responses to all vaccine antigens, 1 month post-dose 3. Solicited symptoms (local and general) were recorded during 4 days, and unsolicited adverse events (AEs) during 31 days, after each vaccination. Serious AEs (SAEs) were recorded throughout the study duration. The immunogenicity of the pentavalent DTPa-IPV/Hib vaccine was non-inferior compared to concomitant administration of DTPa-IPV+Hib vaccines. One month post-dose 3, nearly all infants had antibody levels above the seroprotective thresholds for anti-diphtheria toxoid, anti-tetanus toxoid, anti-polyribosyl-ribitol phosphate, and anti-poliovirus type 1, 2 and 3, and had antibody levels above the seropositive thresholds for anti-pertussis toxoid (PT), anti-filamentous hemagglutinin (FHA) and anti-pertactin (PRN) antibodies. A vaccine response for PT, FHA and PRN was observed in at least 96.7% of study participants. Anti-PRP geometric mean concentrations appeared lower for the DTPa-IPV/Hib group (8.456 µg/mL) than for the DTPa-IPV+Hib group (18.700 µg/mL). In both groups, the most common solicited symptoms were injection site redness and irritability. Fifty-seven SAEs were reported throughout the study; none were considered to be vaccination related.

摘要

我们评估了三剂基础免疫接种方案中含白喉-破伤风-无细胞百日咳-灭活脊髓灰质炎/流感嗜血杆菌疫苗(DTpa-IPV/Hib)在韩国婴儿中的免疫原性和安全性。在这项 III 期、开放性、多中心研究(NCT01309646)中,42-69 日龄(随机 1:1)的健康婴儿接受 3 剂单价 DTpa-IPV/Hib(DTpa-IPV/Hib 组)或分别接种 DTpa-IPV 和 Hib 疫苗(DTpa-IPV+Hib 组),于 2、4、6 月龄。主要目的是证明在第 3 剂后 1 个月,所有疫苗抗原的免疫应答方面,DTpa-IPV/Hib 不劣于 DTpa-IPV+Hib 疫苗。在第 3 剂后 4 天内记录有针对性的症状(局部和全身),在第 31 天内记录未报告的不良事件(AE)。整个研究期间记录严重不良事件(SAE)。五价 DTpa-IPV/Hib 疫苗的免疫原性与同时接种 DTpa-IPV+Hib 疫苗相当。第 3 剂后 1 个月,几乎所有婴儿的抗白喉类毒素、破伤风类毒素、无细胞百日咳多糖、脊髓灰质炎病毒 1、2 和 3 的抗体水平均高于血清保护阈值,对百日咳毒素(PT)、丝状血凝素(FHA)和 pertactin(PRN)抗体的抗体水平高于血清阳性阈值。至少 96.7%的研究参与者观察到对 PT、FHA 和 PRN 的疫苗反应。DTpa-IPV/Hib 组的抗 PRP 几何平均浓度(8.456µg/mL)低于 DTpa-IPV+Hib 组(18.700µg/mL)。在两组中,最常见的有针对性的症状是注射部位发红和烦躁。整个研究期间共报告了 57 例 SAE;均与疫苗接种无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d9d/6422512/0bb53a7a71d5/khvi-15-02-1536588-g001.jpg

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