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

被引:91
作者
Saul, A
Lawrence, G
Allworth, A
Elliott, S
Anderson, K
Rzepczyk, C
Martin, LB
Taylor, D
Eisen, DP
Irving, DO
Pye, D
Crewther, PE
Hodder, AN
Murphy, VJ
Anders, RF
机构
[1] Cooperat Res Ctr Vaccine Technol, Brisbane, Qld, Australia
[2] Queensland Inst Med Res, Brisbane, Qld 4006, Australia
[3] Royal Brisbane Hosp, Brisbane, Qld 4029, Australia
[4] Vaccine Solut Pty Ltd, Brisbane, Qld 4029, Australia
[5] Biotech Australia Pty Ltd, Sydney, NSW, Australia
[6] CSL Ltd, Melbourne, Vic, Australia
[7] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3050, Australia
[8] La Trobe Univ, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
AMA1; P; falciparum; phase 1 vaccine trial;
D O I
10.1016/j.vaccine.2004.09.040
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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 mu g, 20 mu g or 80 mu g 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. (c) 2005 Published by Elsevier Ltd.
引用
收藏
页码:3076 / 3083
页数:8
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