首页> 美国卫生研究院文献>Clinical and Diagnostic Laboratory Immunology >Persistence of Rabies Antibody 5 Years after Postexposure Prophylaxis with Vero Cell Antirabies Vaccine and Antibody Response to a Single Booster Dose
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Persistence of Rabies Antibody 5 Years after Postexposure Prophylaxis with Vero Cell Antirabies Vaccine and Antibody Response to a Single Booster Dose

机译:Vero细胞抗狂犬病疫苗暴露后预防后五年对狂犬病抗体的持久性和对单一加强剂量的抗体反应

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摘要

This study was done to investigate the antibody response to a Vero cell antirabies vaccine, the persistence of antibody for 5 years, and the effect of a booster dose after this interval. From August 2005 to February 2011, a total of 195 patients were enrolled into our study due to an animal bite. The Essen intramuscular (i.m.) regimen, which is recommended by the WHO for modern vaccines used in postexposure treatment, was adopted in this study. Blood samples were obtained on day 0, day 7, day 14, day 45, year 1, year 2, year 3, year 4, year 5, and year 5 plus 14 days. Immunogenicity was evaluated by the titration of neutralizing antibodies with a rapid fluorescent focus inhibition test (RFFIT). Seroconversion was expressed as the seroconversion rate (SCR). A secondary quantitative evaluation criterion, other than the seroconversion level, was the geometric mean titer (GMT). Of the 195 enrolled patients, 168 (86.4%) of them completed the whole study. No serious adverse reactions to the vaccine were reported during vaccination, the 5-year follow-up period, or revaccination. On day 14, the rabies antibody GMT value was 8.87 IU/ml in the vaccinees. During the next 5 years, the SCR in the ChengDa vaccine group gradually decreased to 34.0% at year 5, down from 90.5% at year 1. There was a significant booster effect: the GMT was 15.22 IU/ml on year 5 plus 14 days. Our findings demonstrate that the ChengDa rabies vaccine offers an alternative with a high degree of efficacy and yet limited side effects and ensures that the exposed patient will be on the safe side of the risk of rabies by the 14th day. Moreover, when followed by a booster dose 5 years later, it could boost the immunity. A further booster is effective in inducing a good neutralizing antibody response even after an interval of 5 years.
机译:进行这项研究是为了研究对Vero细胞抗狂犬病疫苗的抗体反应,抗体的持续5年以及在此间隔后加强剂量的影响。从2005年8月到2011年2月,由于动物咬伤,共有195名患者被纳入我们的研究。这项研究采用了WHO推荐的Essen肌内(i.m.)方案,用于暴露后治疗中使用的现代疫苗。在第0天,第7天,第14天,第45天,第1年,第2年,第3年,第4年,第5年和第5年加上14天获得血液样本。通过快速荧光聚焦抑制试验(RFFIT)滴定中和抗体来评估免疫原性。血清转化率表示为血清转化率(SCR)。除血清转化水平外,第二定量评估标准是几何平均滴度(GMT)。在195名登记患者中,其中168名(86.4%)完成了整个研究。在疫苗接种,5年随访期或再接种期间,未报告有严重的疫苗不良反应。在第14天,疫苗中狂犬病抗体的GMT值为8.87 IU / ml。在接下来的5年中,成大疫苗组的SCR从第1年的90.5%逐渐降低到第5年的34.0%。产生了显着的增强作用:第5年+ 14天的GMT为15.22 IU / ml。 。我们的发现表明,成达狂犬病疫苗提供了一种替代方案,具有高度的疗效,但副作用有限,并确保暴露的患者在第14天处于狂犬病风险的安全方面。此外,如果在5年后加强剂量,则可以增强免疫力。甚至在间隔5年后,进一步的加强剂仍可有效诱导良好的中和抗体反应。

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