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Immunogenicity, safety and antibody persistence of a purified vero cell cultured rabies vaccine (Speeda) administered by the Zagreb regimen or Essen regimen in post-exposure subjects

机译:纯化的Vero细胞培养的狂犬病患者(Speya)在暴露后受试者中施用的纯化的Vero细胞培养的狂犬病疫苗(Speya)的免疫原性,安全性和抗体持续性

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摘要

Aim: To compare the safety, immunogenicity and long-term effect of a purified vero cell cultured rabies vaccine in post-exposure subjects following 2 intramuscular regimens, Zagreb or Essen regimen. Methods: Serum samples were collected before vaccination and on days 7, 14, 42, 180 and 365 post vaccination. Solicited adverse events were recorded for 7 d following each vaccine dose, and unsolicited adverse events throughout the entire study period. This study was registered with ClinicalTrials.gov (NCT01821911 and NCT01827917). Results: No serious adverse events were reported. Although Zagreb regimen had a higher incidence of adverse reactions than Essen regimen at the first and second injection, the incidence was similar at the third and fourth injection between these 2 groups as well. At day 42, 100% subjects developed adequate rabies virus neutralizing antibody concentrations ( 0.5IU/ml) for both regimens. At days 180 and 365, the antibody level decreased dramatically, however, the percentage of subjects with adequate antibody concentrations still remained high (above 75% and 50% respectively). None of confirmed rabies virus exposured subjects had rabies one year later, and percentage of subjects with adequate antibody concentrations reached 100% at days 14 and 42. Conclusions: Rabies post-exposure prophylaxis vaccination with PVRV following a Zagreb regimen had a similar safety, immunogenicity and long-term effect to the Essen regimen in China.
机译:目的:比较纯化的Vero细胞培养狂犬病疫苗在2颗肌内治疗中,Zagreb或Espen方案后纯化的Vero细胞培养狂犬病疫苗的安全性,免疫原性和长期效应。方法:在接种疫苗之前,在第7,14,42,180和365天疫苗接种前收集血清样品。在整个研究期间,在每种疫苗剂量和未经请求的不良事件之后记录征集的不良事件7 D.本研究在ClinicalTrials.gov(NCT01821911和NCT01827917)注册。结果:报告了没有严重的不良事件。尽管Zagreb方案在第一和第二次注射时比Essen方案具有更高的不良反应的发生率,但在这两个组之间的第三和第四次注射时,该发病率相似。在第42天,100%受试者开发了适用于两种方案的狂犬病病毒中和抗体浓度(0.5IU / mL)。在第180和365天,抗体水平显着降低,然而,具有足够抗体浓度的受试者的百分比仍然保持高(分别为75%和50%)。一年后没有证实的狂犬病病毒未经狂犬病,并且在14天和第42天具有足够抗体浓度的受试者的百分比达到100%。结论:狂犬病后暴露后暴露的预防疫苗接种Zagreb方案后的PVRV具有相似的安全性,免疫原性。对中国埃森方案的长期影响。

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  • 作者单位

    Chaoyang Dist Ctr Dis Control &

    Prevent 25 Huaweili Beijing 100021 Peoples R China;

    Liaoning Chengda Biol Ltd Share Ltd Shenyang Peoples R China;

    Guangdong Prov Ctr Dis Control &

    Prevent Guangzhou Guangdong Peoples R China;

    Wuhan City Ctr Dis Control &

    Prevent Wuhan Peoples R China;

    Guizhou Prov Ctr Dis Control &

    Prevent Guiyang Peoples R China;

    Hunan Prov Ctr Dis Control &

    Prevent Changsha Hunan Peoples R China;

    Natl Inst Food &

    Drug Control Beijing Peoples R China;

    Chaoyang Dist Ctr Dis Control &

    Prevent 25 Huaweili Beijing 100021 Peoples R China;

    Chaoyang Dist Ctr Dis Control &

    Prevent 25 Huaweili Beijing 100021 Peoples R China;

    Chaoyang Dist Ctr Dis Control &

    Prevent 25 Huaweili Beijing 100021 Peoples R China;

    Chaoyang Dist Ctr Dis Control &

    Prevent 25 Huaweili Beijing 100021 Peoples R China;

    Chaoyang Dist Ctr Dis Control &

    Prevent 25 Huaweili Beijing 100021 Peoples R China;

    Chaoyang Dist Ctr Dis Control &

    Prevent 25 Huaweili Beijing 100021 Peoples R China;

    Guizhou Prov Ctr Dis Control &

    Prevent Guiyang Peoples R China;

    Chaoyang Dist Ctr Dis Control &

    Prevent 25 Huaweili Beijing 100021 Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学免疫学;
  • 关键词

    Post-exposure; Protective effect; Rabies vaccine; Safety; Immunogenicity;

    机译:暴露后;保护作用;狂犬病疫苗;安全;免疫原性;

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