首页> 美国卫生研究院文献>Current Therapeutic Research Clinical and Experimental >A comparison of the tolerability of two dilution volumes (0.5 mL and 1.0 mL) of a purified chick embryo cell rabies vaccine administered intramuscularly to healthy adult volunteers: A randomized intraindividual assessor-blind study
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A comparison of the tolerability of two dilution volumes (0.5 mL and 1.0 mL) of a purified chick embryo cell rabies vaccine administered intramuscularly to healthy adult volunteers: A randomized intraindividual assessor-blind study

机译:对健康成人志愿者肌肉内注射纯化的鸡胚细胞狂犬病疫苗的两种稀释量(0.5 mL和1.0 mL)的耐受性比较:一项随机非个体评估者盲研究

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>Background: The current recommendation of the manufacturer for administering purified chick embryo cell rabies vaccine (PCECV) is to reconstitute the contents with 1.0 mL of water for injection (WFI). However, it has been debated whether a lower volume of WFI (0.5 mL) is likely to cause less pain.>Objectives: The aims of this study were to compare the tolerability of PCECV administered IM at a volume of 0.5 mL versus 1.0 mL of diluent and to determine the immunogenicity of the vaccine when administered according to the World Health Organization-recommended preexposure prophylaxis regimen for rabies immunization.>Methods: This comparative, intraindividual, assessor-blind study was conducted at the Department of Clinical Pharmacology, Topiwala National Medical College and Bai Yamunabai Laxman Nair Charitable Hospital Mumbai, India). Healthy volunteers aged 18 to 50 years received, by randomized sequence, 3 IM injections of PCECV, diluted in 0.5 mL or 1.0 mL of WFI, on study days 0, 7, and 28. Tolerability was assessed at 30 minutes and 24 hours after injection and included assessments for local and systemic reactions. For immunogenicity assessment, rabies virus-neutralizing antibody 0RVNA) titers were assayed at baseline and on day 49 (ie, 3 weeks after the third injection).>Results: Twenty-six subjects (24 men, 2 women; mean [SD] age, 22.4 [2.4] years; mean [SD] body weight, 59.0 [11.3] kg) entered the study. Twenty-five subjects were included in the tolerability assessment; 24 in the immunogenicity assessment. No statistically significant differences were found between dilutions in the frequency of local and systemic reactions. Most reactions were mild. All subjects developed RVNA titers >0.5 IU/mL (indicative of protection) by day 49.>Conclusions: In this population of healthy volunteers, a full antigenic dose of PCECV in a dilution of 0.5 mL WFI is as well tolerated locally and systemically as in a dilution of 1.0 mL. All subjects developed levels of RVNA far exceeding 0.5 IU/mL, which is indicative of protection against rabies.
机译:>背景:制造商目前对纯化的鸡胚细胞狂犬病疫苗(PCECV)的管理建议是用1.0 mL注射用水(WFI)稀释内含物。然而,一直存在争议的是,较低量的WFI(0.5 mL)是否可能减轻疼痛。>目的:本研究的目的是比较PCECV给予IM的耐受性。分别使用0.5 mL和1.0 mL稀释剂,并根据世界卫生组织推荐的用于狂犬病免疫的暴露前预防方案来确定疫苗的免疫原性。>方法:由印度托皮瓦拉国立医学院临床药理学系和印度孟买Bai Yamunabai Laxman Nair慈善医院进行。在研究的第0、7和28天,随机抽取年龄在18至50岁的健康志愿者接受3次IM注射的PCECV注射,分别稀释在0.5 mL或1.0 mL WFI中。在注射后30分钟和24小时评估耐受性并包括对局部和全身反应的评估。为了进行免疫原性评估,在基线和第49天(即第三次注射后3周)测定了狂犬病毒中和抗体0RVNA的效价。>结果: 26名受试者(24名男性,2名女性) ;平均[SD]年龄22.4 [2.4]岁;平均[SD]体重59.0 [11.3] kg)进入研究。 25名受试者被纳入耐受性评估; 24在免疫原性评估中。在局部和全身反应的频率之间稀释之间没有发现统计学上的显着差异。大多数反应是轻微的。到第49天,所有受试者的RVNA滴度均> 0.5 IU / mL(表明有保护作用)。>结论:在这批健康志愿者中,0.5mL WFI稀释液中的全抗原剂量PCECV为在1.0 mL稀释液中,局部和全身耐受性良好。所有受试者的RVNA水平均远超过0.5 IU / mL,这表明可以预防狂犬病。

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