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A human phase 1 vaccine clinical trial of the Plasmodium falciparum malaria vaccine candidate apical membrane antigen 1 in Montanide ISA720 adjuvant

机译:Montanide ISA720佐剂中恶性疟原虫疟疾疫苗候选顶膜抗原1的人类1期疫苗临床试验

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摘要

A dose escalating, placebo-controlled phase 1 trial was conducted to test the safety and immunogenicity of a vaccine containing recombinant Plasmodium falciparum apical membrane antigen 1 (AMA1) formulated in Montanide ISA720. Three groups of volunteers were vaccinated intramuscularly with 5 microg, 20 microg or 80 microg of AMA1, respectively, in 0.5 mL of formulation at 0, 3 and 6 months. Anti-AMA1 antibody levels and T cell stimulation indices were measured before and after each vaccination. No vaccine-related serious adverse events were recorded. Most subjects generated a mild to moderate, transient local reaction after the first vaccination. Three subjects developed a local reaction approximately 10 days following vaccination. Six of the 29 subjects seroconverted. Only one of these developed a high antibody titre. However, the interpretation of this trial was compromised by a loss of potency of the formulated vaccine during the course of the study.
机译:进行了剂量递增,安慰剂对照的1期试验,以测试包含在Montanide ISA720中配制的重组恶性疟原虫顶端膜抗原1(AMA1)的疫苗的安全性和免疫原性。在0、3和6个月时,分别在0.5 mL制剂中分别对3组志愿者进行肌肉内接种5微克,20微克或80微克的AMA1。在每次接种之前和之后测量抗AMA1抗体水平和T细胞刺激指数。没有记录到疫苗相关的严重不良事件。大多数受试者在初次接种疫苗后产生轻度至中度的暂时性局部反应。疫苗接种后约10天,三名受试者出现局部反应。 29名受试者中有6名血清转化。这些中只有一个产生高抗体滴度。但是,由于在研究过程中配制疫苗的效力丧失,因此对该试验的解释受到了损害。

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