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Vi-破伤风类毒素结合伤寒疫苗(PedaTyph™)在印度儿童中的有效性和安全性:基于学校的整群随机研究。

Efficacy and safety of vi-tetanus toxoid conjugated typhoid vaccine (PedaTyph™) in Indian children: School based cluster randomized study.

作者信息

Mitra Monjori, Shah Nitin, Ghosh Apurba, Chatterjee Suparna, Kaur Iqbal, Bhattacharya Nisha, Basu Suparna

机构信息

a Institute of Child Health , Kolkata , India.

b Department of Pediatrics , Lion's Tarachand Bapa Hospital, Sion West , Mumbai , India.

出版信息

Hum Vaccin Immunother. 2016 Apr 2;12(4):939-45. doi: 10.1080/21645515.2015.1117715. Epub 2016 Feb 22.

Abstract

Vi polysaccharide typhoid vaccines cannot be used in children <2 years owing to poor immunogenic and T cell independent properties. Conjugate vaccine prepared by binding Vi to tetanus toxoids (Vi-TT) induces protective levels even in children <2 years. We evaluated efficacy and safety following vaccination with a Vi-TT vaccine in children 6 months to 12 years of age. Overall, 1765 subjects were recruited from two registered municipal urban slums of southern Kolkata. Most of the children of the slum dwellers attended the schools in the locality which was selected with permission from the school authority. Schools were randomly divided into vaccinated (Test group) and unvaccinated group (Control group). Children and their siblings of test group received 2-doses of PedaTyph™ vaccine at 6 weeks interval. Control group received vaccines as per national guidelines. Adverse events (AEs) were examined after 30 minutes, 1 month and clinical events were observed till 12 months post-vaccination. Incidence of culture positive typhoid fever in the control group was 1.27% vis-a-vis none in vaccine group during 12 months. In subgroup evaluated for immunogenicity, an antibody titer value of 1.8 EU/ml (95% CI: 1.5 EU/ml, 2.2 EU/ml), 32 EU/ml (95% CI: 27.0 EU/ml, 39.0 EU/ml) and 14 EU/ml (95% CI: 12.0 EU/ml, 17.0 EU/ml) at baseline, 6 weeks and 12 months, respectively was observed. Sero-conversion among the sub-group was 100% after 6 weeks of post-vaccination and 83% after 12 months considering 4-fold rise from baseline. The efficacy of vaccine was 100 % (95% CI: 97.6%, 100%) in the first year of follow-up with minimal AEs post vaccination. Vi conjugate typhoid vaccine conferred 100% protection against typhoid fever in 1765 children 6 months to 12 years of age with high immunogenicity in a subgroup from the vaccine arm.

摘要

Vi多糖伤寒疫苗不能用于2岁以下儿童,因为其免疫原性差且具有非T细胞依赖性。通过将Vi与破伤风类毒素结合制备的结合疫苗(Vi-TT)即使在2岁以下儿童中也能诱导出保护性水平。我们评估了6个月至12岁儿童接种Vi-TT疫苗后的疗效和安全性。总体而言,从加尔各答南部两个注册的城市贫民窟招募了1765名受试者。贫民窟居民的大多数孩子在当地学校上学,这些学校是在获得学校当局许可后挑选出来的。学校被随机分为接种组(试验组)和未接种组(对照组)。试验组的儿童及其兄弟姐妹每隔6周接种2剂PedaTyph™疫苗。对照组按照国家指南接种疫苗。接种后30分钟、1个月检查不良事件(AE),并观察临床事件直至接种后12个月。在12个月期间,对照组中培养阳性伤寒热的发病率为1.27%,而疫苗组中无一例发病。在评估免疫原性的亚组中,基线、6周和12个月时的抗体滴度值分别为1.8 EU/ml(95%CI:1.5 EU/ml,2.2 EU/ml)、32 EU/ml(95%CI:27.0 EU/ml,39.0 EU/ml)和14 EU/ml(95%CI:12.0 EU/ml,17.0 EU/ml)。接种疫苗6周后亚组中的血清转化率为100%,接种后12个月考虑到较基线上升4倍时为83%。在随访的第一年,疫苗的疗效为100%(95%CI:97.6%,100%),接种后不良事件最少。Vi结合伤寒疫苗在1765名6个月至12岁儿童中对伤寒热提供了100%的保护,在疫苗组的一个亚组中具有高免疫原性。

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