Chiodi F, von Gegerfeldt A, Albert J, Fenyö E M, Gaines H, von Sydow M, Biberfeld G, Parks E, Norrby E
Department of Virology, Karolinska Institute School of Medicine, Stockholm, Sweden.
J Med Virol. 1987 Sep;23(1):1-9. doi: 10.1002/jmv.1890230102.
Two partially overlapping 19 and 22 amino acids long peptides representing a highly immunogenic site of the transmembranous glycoprotein (gp41) of human immunodeficiency virus (HIV) were used as antigen in ELISA tests. The results of antibody determination with this assay were compared with those of three or more conventional ELISAs and Western blot (WB) tests and radioimmunoprecipitation assay. Twenty-six sera from patients with AIDS or LAS and from asymptomatic carriers of HIV infection all showed a pronounced reaction in the peptide ELISA as well as positive results with other tests. In contrast, 27 sera from laboratory workers and blood donors were negative by all tests. A group of 39 blood donor sera, which had shown false positive or ambiguous results in the ELISAs and sometimes in WB tests employed for confirmation, also were negative in all cases with the peptide ELISA. Consecutive samples collected from individuals with primary HIV infection were also analyzed. In 6 out of 9 cases, the peptide ELISA revealed an antibody response within one month after onset of clinical symptoms and sensitivity for antibody detection equaled that of other ELISA tests. Eight sera from five West African persons infected with HIV-related viruses did not react in the peptide ELISA, reflecting differences in properties of the envelope components. The peptide ELISA used in this study appears to represent a simple technique employing chemically synthesized antigen for accurate and sensitive estimation of antibodies to the HIV group of nontransforming human retroviruses.
两条长度分别为19个和22个氨基酸的部分重叠肽段,代表人类免疫缺陷病毒(HIV)跨膜糖蛋白(gp41)的一个高免疫原性位点,被用作酶联免疫吸附测定(ELISA)试验的抗原。将该测定法的抗体检测结果与三种或更多种传统ELISA、蛋白质印迹(WB)试验及放射免疫沉淀测定法的结果进行比较。来自艾滋病患者、艾滋病相关综合征(LAS)患者以及HIV感染无症状携带者的26份血清在肽段ELISA中均显示出明显反应,且其他检测结果也呈阳性。相比之下,来自实验室工作人员和献血者的27份血清在所有检测中均为阴性。一组39份献血者血清,在用于确认的ELISA中有时在WB试验中显示出假阳性或不明确结果,但在肽段ELISA中所有病例均为阴性。对原发性HIV感染个体采集的连续样本也进行了分析。在9例中的6例中,肽段ELISA在临床症状出现后1个月内显示出抗体反应,其抗体检测灵敏度与其他ELISA试验相当。来自5名感染HIV相关病毒的西非人的8份血清在肽段ELISA中无反应,这反映了包膜成分特性的差异。本研究中使用的肽段ELISA似乎是一种采用化学合成抗原的简单技术,用于准确、灵敏地估计针对非转化型人类逆转录病毒HIV组的抗体。