Cheung A, Leban J, Shaw A R, Merkli B, Stocker J, Chizzolini C, Sander C, Perrin L H
Proc Natl Acad Sci U S A. 1986 Nov;83(21):8328-32. doi: 10.1073/pnas.83.21.8328.
Polypeptides expressed on the surface of merozoites, the invasive stage of the asexual blood cycle, are good candidates for the development of malaria vaccines. Five synthetic peptides with predetermined specificity deduced from a genomic DNA clone coding for the NH2-terminal portion of the main merozoite surface polypeptide of Plasmodium falciparum were evaluated for their capability to raise antibodies that react with the P. falciparum merozoites. Antibodies induced by two of the peptides (3 and 5) reacted with the membrane surfaces of seven of seven isolates of P. falciparum from different geographic areas. Antibodies against peptide 4, which contains a repeated amino acid sequence (Gly-Gly-Ser and Val-Ala-Ser), reacted with six of seven isolates. Structural analysis of the deduced polypeptides suggests that peptide 3 is exposed at the surface of merozoites. When it was used to immunize monkeys, three of the four animals were partially protected from a challenge infection that induced a fulminant infection in control animals.
疟原虫无性血液周期中的侵入阶段即裂殖子表面表达的多肽,是开发疟疾疫苗的良好候选物。从编码恶性疟原虫主要裂殖子表面多肽NH2末端部分的基因组DNA克隆推导出来的具有预定特异性的五种合成肽,被评估了其产生与恶性疟原虫裂殖子发生反应的抗体的能力。由其中两种肽(3号和5号)诱导产生的抗体与来自不同地理区域的七株恶性疟原虫分离株中的七株的膜表面发生了反应。针对含有重复氨基酸序列(甘氨酸-甘氨酸-丝氨酸和缬氨酸-丙氨酸-丝氨酸)的4号肽的抗体与七株分离株中的六株发生了反应。对推导多肽的结构分析表明,3号肽暴露于裂殖子表面。当用其免疫猴子时,四只动物中有三只受到了部分保护,免受了在对照动物中引发暴发性感染的攻击感染。