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首页> 外文期刊>The Pediatric infectious disease journal >Revaccination with locally-produced vi typhoid polysaccharide vaccine among chinese school-aged children: safety and immunogenicity findings.
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Revaccination with locally-produced vi typhoid polysaccharide vaccine among chinese school-aged children: safety and immunogenicity findings.

机译:在中国学龄儿童中用本地生产的vi伤寒多糖疫苗进行再接种:安全性和免疫原性研究结果。

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摘要

OBJECTIVE: To evaluate the safety and immunogenicity of revaccination with locally-produced Vi polysaccharide vaccine 3 years after the first dose in Chinese children aged 9 to 14 years. METHODS: A randomized, placebo-controlled trial was conducted in Suzhou, Jiangsu, China. Six hundred and sixty-seven eligible children who had previously received a primary dose of Vi vaccine were randomly assigned to receive 1 dose of 30 mug Vi vaccine or placebo. In addition, 331 eligible children received 1 dose of Vi polysaccharide vaccine as a primary vaccination. Adverse events were followed for 28 days after vaccination. Serum samples were collected from a subgroup of participants on day 0 and day 28, and Vi antibodies were analyzed using a passive hemagglutination method. RESULTS: Revaccination was found to be safe and immunogenic. No severe adverse events were observed. A significant increase in antibody titers after vaccination was observed among children who had and had not been previously vaccinated. Twenty-eight days after injection, the seropositive rate was 79% in both revaccination and primary injection groups; the geometric mean antibody titer was 1:40 in the primary injection group and 1:29 in the revaccination group (P = 0.24). Although the difference of attained geometric mean titers in follow-up sera was not significantly different in these 2 groups, the fold-rise of these titers from baseline was significantly higher in the primary injection group than in the revaccination group (7.7 versus 3.1, P < 0.001). CONCLUSION: We found that revaccination using the locally produced Vi polysaccharide vaccine among Chinese school-aged children was safe and increased antibody titers. Revaccination can be used to extend the duration of protection provided by Vi polysaccharide vaccine.
机译:目的:评估9至14岁中国儿童首次接种后3年用当地生产的Vi多糖疫苗进行再接种的安全性和免疫原性。方法:在中国江苏省苏州市进行的一项随机,安慰剂对照试验。先前曾接受第一剂Vi疫苗的667名合格儿童被随机分配接受1剂30杯Vi疫苗或安慰剂。此外,有331名合格儿童接受了1剂Vi多糖疫苗的初次接种。接种疫苗后28天进行不良事件追踪。在第0天和第28天从参与者的亚组收集血清样品,并使用被动血凝法分析Vi抗体。结果:重新接种被认为是安全的和免疫原性的。没有观察到严重的不良事件。在以前接种过和未接种过疫苗的儿童中,接种疫苗后的抗体滴度显着增加。注射后28天,再次注射组和初次注射组的血清阳性率均为79%。在初次注射组中,抗体的几何平均滴度为1:40,在再接种组中为1:29(P = 0.24)。尽管两组的随访血清中几何平均滴度的差异无显着差异,但初次注射组的这些滴度相对于基线的倍数升高明显高于再接种组(7.7 vs 3.1,P <0.001)。结论:我们发现,在中国学龄儿童中使用本地生产的Vi多糖疫苗进行再接种是安全的,并且抗体效价更高。再接种可用于延长Vi多糖疫苗提供的保护时间。

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