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在日本婴儿中,将白喉、破伤风、无细胞百日咳和源自萨宾株的灭活脊髓灰质炎病毒疫苗(DTaP-sIPV)与五价轮状病毒疫苗联合接种。

Concomitant administration of diphtheria, tetanus, acellular pertussis and inactivated poliovirus vaccine derived from Sabin strains (DTaP-sIPV) with pentavalent rotavirus vaccine in Japanese infants.

作者信息

Tanaka Yoshiyuki, Yokokawa Ruriko, Rong Han Shi, Kishino Hiroyuki, Stek Jon E, Nelson Margaret, Lawrence Jody

机构信息

a Japan Development , MSD K.K., Tokyo , Japan.

b Merck Sharp & Dohme Corp. , Kenilworth , NJ , USA.

出版信息

Hum Vaccin Immunother. 2017 Jun 3;13(6):1-7. doi: 10.1080/21645515.2017.1279769. Epub 2017 Jan 31.

Abstract

Rotavirus is the leading cause of severe acute gastroenteritis in infants and young children. Most children are infected with rotavirus, and the health and economic burdens of rotavirus gastroenteritis on healthcare systems and families are considerable. In 2012 pentavalent rotavirus vaccine (RV5) and diphtheria, tetanus, acellular pertussis and inactivated poliovirus vaccine derived from Sabin strains (DTaP-sIPV) were licensed in Japan. We examined the immunogenicity and safety of DTaP-sIPV when administrated concomitantly with RV5 in Japanese infants. A total of 192 infants 6 to 11 weeks of age randomized to Group 1 (N = 96) received DTaP-sIPV and RV5 concomitantly, and Group 2 (N = 96) received DTaP-sIPV and RV5 separately. Antibody titer to diphtheria toxin, pertussis antigens (PT and FHA), tetanus toxin, and poliovirus type 1, 2, and 3 were measured at 4 to 6 weeks following 3-doses of DTaP-sIPV. Seroprotection rates for all components of DTaP-sIPV were 100% in both groups, and the geometric mean titers for DTaP-sIPV in Group 1 were comparable to Group 2. Incidence of systemic AEs (including diarrhea, vomiting, fever, and nasopharyngitis) were lower in Group 1 than in Group 2. All vaccine-related AEs were mild or moderate in intensity. There were no vaccine-related serious AEs, no deaths, and no cases of intussusception during the study. Concomitant administration of DTaP-sIPV and RV5 induced satisfactory immune responses to DTaP-sIPV and acceptable safety profile. The administration of DTaP-sIPV given concomitantly with RV5 is expected to facilitate compliance with the vaccination schedule and improve vaccine coverage in Japanese infants.

摘要

轮状病毒是婴幼儿严重急性胃肠炎的主要病因。大多数儿童都会感染轮状病毒,轮状病毒胃肠炎给医疗系统和家庭带来的健康和经济负担相当大。2012年,五价轮状病毒疫苗(RV5)以及源自萨宾株的白喉、破伤风、无细胞百日咳和灭活脊髓灰质炎病毒疫苗(DTaP-sIPV)在日本获得许可。我们研究了DTaP-sIPV与RV5同时接种时在日本婴儿中的免疫原性和安全性。总共192名6至11周龄的婴儿被随机分为第1组(N = 96),同时接种DTaP-sIPV和RV5;第2组(N = 96)分别接种DTaP-sIPV和RV5。在3剂DTaP-sIPV接种后4至6周测量对白喉毒素、百日咳抗原(PT和FHA)、破伤风毒素以及1型、2型和3型脊髓灰质炎病毒的抗体滴度。两组中DTaP-sIPV所有成分的血清保护率均为100%,第1组中DTaP-sIPV的几何平均滴度与第2组相当。第1组全身不良事件(包括腹泻、呕吐、发热和鼻咽炎)的发生率低于第2组。所有与疫苗相关的不良事件强度均为轻度或中度。研究期间未出现与疫苗相关的严重不良事件、死亡病例和肠套叠病例。DTaP-sIPV与RV5同时接种诱导了对DTaP-sIPV令人满意的免疫反应和可接受的安全性。预计DTaP-sIPV与RV5同时接种将有助于遵守疫苗接种计划并提高日本婴儿的疫苗接种覆盖率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb7/5489296/53d058ccece8/khvi-13-06-1279769-g001.jpg

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