Leach A, Drakeley C J, D'Alessandro U, Fegan G W, Bennett S, Ballou W R, Targett G A, Greenwood B M
MRC Laboratories, Fajara, Banjul, The Gambia.
Parasite Immunol. 1995 Aug;17(8):441-4. doi: 10.1111/j.1365-3024.1995.tb00912.x.
A pilot safety and immunogenicity trial of the malaria vaccine SPf66 has been undertaken in 150 Gambian infants. No significant systemic side effects were recorded but modest local reactions were seen after the administration of a third 1.0 mg dose. SPf66 produced in Colombia was more immunogenic than SPf66 produced in the USA and a 1.0 mg dose of each vaccine gave higher antibody levels than a 0.5 mg dose. However, antibody levels fell rapidly after administration of the third dose of vaccine and showed little change over the following malaria transmission season. The incidence of clinical malaria was higher among children who received SPf66 than among children who received inactivated polio vaccine, the effect being most marked among children who received 1.0 mg Colombian SPf66. As the trial was not designed to measure the effect of SPf66 on morbidity from malaria, the significance of this finding is uncertain.
已在150名冈比亚婴儿中开展了疟疾疫苗SPf66的安全性和免疫原性初步试验。未记录到明显的全身性副作用,但在接种第三剂1.0毫克剂量后出现了轻微的局部反应。在哥伦比亚生产的SPf66比在美国生产的SPf66免疫原性更强,每种疫苗1.0毫克剂量产生的抗体水平高于0.5毫克剂量。然而,在接种第三剂疫苗后抗体水平迅速下降,并且在随后的疟疾传播季节几乎没有变化。接种SPf66的儿童中临床疟疾的发病率高于接种灭活脊髓灰质炎疫苗的儿童,这一效应在接种1.0毫克哥伦比亚SPf66的儿童中最为明显。由于该试验并非旨在测量SPf66对疟疾发病率的影响,这一发现的意义尚不确定。