Rodriguez R, Moreno A, Guzman F, Calvo M, Patarroyo M E
Instituto de Inmunologia, Hospital San Juan de Dios, Universidad Nacional de Colombia, Bogotá.
Am J Trop Med Hyg. 1990 Oct;43(4):339-54. doi: 10.4269/ajtmh.1990.43.339.
During the development of a synthetic vaccine for human use against the asexual blood stages of Plasmodium falciparum, monkey trials were performed to assess safety, immunogenicity, and protectivity. We determined the minimal infective dose of the P. falciparum FVO strain, the kinetics of the immune response induced by vaccination with the synthetic peptide mixture (S7 + S12 + S17) or the synthetic hybrid polymeric protein SPf66, and the induction of protective immunity against the experimental challenge with 2 P. falciparum strains. A clear boosting effect was observed, determined by the increased antibody titers against synthetic peptides S7, S12, S17, and SPf66, and by improvement in the protective immune response against the challenge. These studies suggest that either the peptide mixture or the synthetic hybrid polymeric protein are excellent choices for the development of a vaccine against P. falciparum.
在研发用于人类的抗恶性疟原虫无性血液期的合成疫苗过程中,进行了猴子试验以评估安全性、免疫原性和保护性。我们确定了恶性疟原虫FVO株的最小感染剂量、用合成肽混合物(S7 + S12 + S17)或合成杂合聚合蛋白SPf66接种诱导的免疫反应动力学,以及针对两种恶性疟原虫株实验性攻击的保护性免疫诱导情况。通过针对合成肽S7、S12、S17和SPf66的抗体滴度增加以及针对攻击的保护性免疫反应改善,观察到了明显的增强效应。这些研究表明,肽混合物或合成杂合聚合蛋白都是开发抗恶性疟原虫疫苗的极佳选择。