Millet P, Chizzolini C, Wirtz R A, Bathurst I, Broderson J R, Campbell G H, Collins W E
Division of Parasitic Diseases, Centers for Disease Control, Atlanta, GA 30333.
Eur J Immunol. 1992 Feb;22(2):519-24. doi: 10.1002/eji.1830220234.
In previous studies, Saimiri sciureus boliviensis monkeys have been immunized with four recombinant proteins reproducing part of the circumsporozoite (CS) protein of Plasmodium vivax sporozoites (NS1(81) V20, rPvCS-1, rPvCS-2, rPv-CS-3), or with irradiated sporozoites of P. vivax Salvador I strain. To analyze the antibody response elicited against epitopes located outside the immunodominant repeat region of the CS protein, serum samples from these animals were tested for their ability to inhibit the in vitro development of liver stages of P. vivax VK247 strain, characterized from the other strains only by a specific repeat region on the CS protein. Results indicated that there is at least one protective B-cell epitope outside the repeat region of the CS protein of P. vivax sporozoites, and that this epitope can be expressed by irradiated sporozoites, rPvCS-1 and -3, but not by rPvCS-1 or NS1(81)V20. Therefore, we designed peptides from the amino acid sequences present both in rPvCS-2 and -3, but not included in the recombinant proteins rPvCS-1 and NS1(81)V20. Anti-peptide antibodies had no activity on the development of sporozoites of P. vivax Salvador I strain, into schizonts in primary culture of Saimiri monkey hepatocytes. In addition, antisporozoite antibodies did not react with any of the peptides. These results suggest that the in vitro inhibition observed in this study could depend upon the conformation of the CS protein. This study also demonstrates that antibody response to unnatural linear epitopes can be induced by immunization with recombinant proteins.
在先前的研究中,已用四种重组蛋白(它们复制了间日疟原虫子孢子环子孢子蛋白(CS)的部分片段(NS1(81)V20、rPvCS - 1、rPvCS - 2、rPv - CS - 3))或间日疟原虫萨尔瓦多I株的辐照子孢子对松鼠猴进行免疫。为了分析针对CS蛋白免疫显性重复区域之外的表位引发的抗体反应,检测了这些动物的血清样本抑制间日疟原虫VK247株肝期体外发育的能力,该株与其他株的区别仅在于CS蛋白上的一个特定重复区域。结果表明,间日疟原虫子孢子CS蛋白的重复区域之外至少存在一个保护性B细胞表位,并且该表位可由辐照子孢子、rPvCS - 1和 - 3表达,但不能由rPvCS - 1或NS1(81)V20表达。因此,我们根据rPvCS - 2和 - 3中存在但重组蛋白rPvCS - 1和NS1(81)V20中未包含的氨基酸序列设计了肽段。抗肽抗体对间日疟原虫萨尔瓦多I株子孢子在松鼠猴肝细胞原代培养中发育为裂殖体没有活性。此外,抗子孢子抗体与任何一种肽段均无反应。这些结果表明,本研究中观察到的体外抑制可能取决于CS蛋白的构象。本研究还证明,用重组蛋白免疫可诱导对非天然线性表位的抗体反应。