Pessi A, Michel M, Bianchi E, Mendis A, Tougne C, Verdini A S, Lambert P H, Carter R, Mendis K, Del Giudice G
WHO-Immunology Research and Training Center, University of Geneva, Switzerland.
Am J Trop Med Hyg. 1990 Jan;42(1):17-23. doi: 10.4269/ajtmh.1990.42.17.
Synthetic peptides reproducing 4 DRADGQPAG (D4) and a sequential array of DRADGQPAG and DRAAGQPAG repeats (DDAAD) of the Plasmodium vivax circumsporozoite (CS) protein were investigated for their potential use in the detection of P. vivax sporozoite antibodies in human sera. These peptides specifically inhibited the binding of monoclonal antibodies to the P. vivax CS protein in Western blots. However, when D4 and DDAAD peptides were used in an enzyme-linked immunosorbent assay (ELISA) for the detection of human antibodies, more sera bound to the DDAAD (61%) than to the D4 peptide (22%). This binding was specific, and suggested that the DDAAD peptide contained epitopes constituted by the sequential array of DRADGQPAG and DRAAGQPAG repeat variants and absent in the D4 peptide. The ELISA using the DDAAD peptide was applied to the detection of P. vivax CS protein antibodies in a large number of sera from Kataragama, an endemic area in Sri Lanka. The prevalence of these antibodies increased with age, reaching 40% in adults greater than 50 years old. The ELISA employing the DDAAD peptide represents a simple and useful tool for the analysis of the antibody response to P. vivax sporozoites in naturally exposed individuals.
研究了疟原虫环子孢子(CS)蛋白中能复制4个DRADGQPAG(D4)以及DRADGQPAG和DRAAGQPAG重复序列的连续阵列(DDAAD)的合成肽在检测人血清中间日疟原虫子孢子抗体方面的潜在用途。在蛋白质印迹法中,这些肽特异性抑制单克隆抗体与间日疟原虫CS蛋白的结合。然而,当在酶联免疫吸附测定(ELISA)中使用D4和DDAAD肽来检测人抗体时,与DDAAD肽结合的血清(61%)比与D4肽结合的血清(22%)更多。这种结合具有特异性,表明DDAAD肽包含由DRADGQPAG和DRAAGQPAG重复变体的连续阵列构成的表位,而D4肽中不存在这些表位。使用DDAAD肽的ELISA法用于检测来自斯里兰卡流行地区卡塔拉加马的大量血清中的间日疟原虫CS蛋白抗体。这些抗体的流行率随年龄增加,在50岁以上的成年人中达到40%。采用DDAAD肽的ELISA法是分析自然暴露个体对间日疟原虫子孢子抗体反应的一种简单而有用的工具。