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Immunogenicity, safety and lot consistency in adults of achromatographically purified Vero-cell rabies vaccine: a randomized,double-blind trial with human diploid cell rabies vaccine

机译:色谱纯化的Vero细胞狂犬病疫苗在成人中的免疫原性,安全性和批次一致性:人二倍体细胞狂犬病疫苗的随机双盲试验

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The immunogenicity and safety of a chromatographically purified rabies vaccine (CPRV) was evaluated using US veterinary medical students. In the first study, 242 healthy adults were enrolled in a randomized, modified double-blind, multicenter trial and received five doses of either CPRV or human diploid cell vaccine (HDCV) by intramuscular injection on days 0, 3, 7, 14, and 28 concurrently with human rabies immunoglobulin in a simulated post-exposure prophylaxis regimen. Post-immunization titers in the CPRV and HDCV groups reached 0.5 IU/ml (the WHO-recommended minimally acceptable titer) or greater in all subjects in both vaccine groups by day 14 and remained above that level through day 90. In the second study, 438 healthy adults were enrolled in a randomized, double-blind, multicenter trial and assigned to receive five doses from one of three lots of CPRV by intramuscular injection on days 0, 3, 7, 14, and 28 in a simulated post-exposure prophylaxis regimen to evaluate lot consistency. Post-immunization titers rapidly increased to over 0.5 IU/ml by day 14 for all subjects and remained above that level through day 42 when the study was terminated. The three lots were considered equivalent. The percentage of subjects with at least one local reaction during the five-dose regimen was slightly lower in the CPRV group than in the HDCV group (P = 0.06). The most frequently reported local reaction for all doses of vaccine was pain at the injection site. Headache, myalgia, and malaise were the most frequently reported systemic events. The percentage of subjects with at least one systemic event was significantly lower for CPRV (P = 0.0084). No vaccine-related serious adverse reaction was reported in these studies. The results of these studies indicate that CPRV administered intramuscularly to healthy adults is immunogenic and is associated with fewer local and systemic reactions than HDCV.
机译:色谱纯化的狂犬病疫苗(CPRV)的免疫原性和安全性是使用美国兽医学学生进行评估的。在第一个研究中,有242名健康成年人参加了一项随机,改良的双盲,多中心试验,并在第0、3、7、14和8天通过肌肉注射接受了五剂CPRV或人二倍体细胞疫苗(HDCV)。 28在模拟的暴露后预防方案中与人狂犬病免疫球蛋白同时进行。到第14天时,两个疫苗组中所有受试者的CPRV和HDCV组的免疫后滴度均达到0.5 IU / ml(WHO建议的最低可接受滴度)或更高,并在90天之前一直高于该水平。 438名健康成人参加了一项随机,双盲,多中心试验,并在模拟暴露后预防中,分别在第0、3、7、14和28天通过肌肉注射从三批CPRV中的一组中接受了五剂剂量评估批次一致性的方案。到第14天,所有受试者的免疫后效价迅速提高至超过0.5 IU / ml,并且在研究终止时的第42天一直保持在该水平以上。这三个批次被认为是等效的。在五剂方案中发生至少一种局部反应的受试者百分比在CPRV组中比在HDCV组中稍低(P = 0.06)。所有剂量疫苗中最常报告的局部反应是注射部位的疼痛。头痛,肌痛和不适是最常报告的全身事件。 CPRV至少发生一次全身性事件的受试者百分比显着降低(P = 0.0084)。这些研究中没有报道疫苗相关的严重不良反应。这些研究的结果表明,肌肉注射给予健康成年人的CPRV具有免疫原性,并且与HDCV相比,具有较少的局部和全身反应。

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