Lawrence G, Cheng Q Q, Reed C, Taylor D, Stowers A, Cloonan N, Rzepczyk C, Smillie A, Anderson K, Pombo D, Allworth A, Eisen D, Anders R, Saul A
CRC for Vaccine Technology and Australian Centre for International and Tropical Health and Nutrition, The Queensland Institute of Medical Research and The University of Queensland, Post Office, Royal Brisbane Hospital, Brisbane, Australia.
Vaccine. 2000 Mar 17;18(18):1925-31. doi: 10.1016/s0264-410x(99)00444-2.
A placebo controlled, randomised, double blind trial was conducted in human volunteers to test a mixture of three recombinant Plasmodium falciparum blood stage antigens for its ability to reduce the initial growth rates of parasites. The vaccine contained recombinant MSP2 (3D7 allele), a portion of MSP1 (190LCS.T3) and part of the RESA antigen (C terminal 771 amino acids) in the Montanide ISA 720 adjuvant (SEPPIC). Twelve volunteers received two doses of the vaccine, 6 weeks apart. The five participants in the placebo group received an equivalent volume of the adjuvant emulsion using the same schedule. Antibody responses were low, as has been reported in earlier studies with this combination, while T cell responses were stronger. All the volunteers were challenged with approximately 140 ring infected red cells of the 3D7 cloned line, 4 weeks after the second dose. Parasitaemia was determined once daily from day 4 using a sensitive and quantitative PCR assay. All the volunteers were infected and were treated on day 8, before any developed symptoms. There was no significant difference in initial parasite growth rates between the verum and placebo groups, nor was there any significant correlation between parasite growth rates and any of the measured immunological responses. These results suggest that the formulation tested in this trial did not generate immune responses that were strong enough to reduce parasite growth in naive volunteers.
在人类志愿者中进行了一项安慰剂对照、随机、双盲试验,以测试三种重组恶性疟原虫血液期抗原的混合物降低寄生虫初始生长速率的能力。该疫苗含有重组MSP2(3D7等位基因)、一部分MSP1(190LCS.T3)和部分RESA抗原(C末端771个氨基酸),佐剂为Montanide ISA 720(赛比克公司)。12名志愿者接受了两剂疫苗,间隔6周。安慰剂组的5名参与者按照相同的时间表接受了等量的佐剂乳剂。正如早期关于该组合的研究所报道的那样,抗体反应较低,而T细胞反应较强。在第二剂疫苗接种4周后,所有志愿者均受到约140个3D7克隆系的环状感染红细胞的攻击。从第4天起,每天使用灵敏的定量PCR测定法测定疟原虫血症。所有志愿者均被感染,并在第8天出现任何症状之前接受治疗。实验组和安慰剂组之间的初始寄生虫生长速率没有显著差异,寄生虫生长速率与任何测量的免疫反应之间也没有显著相关性。这些结果表明,在该试验中测试的制剂没有产生足够强的免疫反应来降低未感染志愿者体内的寄生虫生长。