首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Discrimination of human T-lymphotropic virus type-I and type-II infections by synthetic peptides representing structural epitopes from the envelope glycoproteins.
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Discrimination of human T-lymphotropic virus type-I and type-II infections by synthetic peptides representing structural epitopes from the envelope glycoproteins.

机译:用代表来自包膜糖蛋白的结构表位的合成肽区分人T型淋巴病毒I型和II型感染。

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摘要

Synthetic peptides representing the immunodominant structural motifs of the envelope region of human T-lymphotropic virus types I (HTLV-I) (Env-1(191-214) and Env-5(242-257)) and II (HTLV-II) (Env-20(85-102 and Env-2(187-209)) were used to develop an enzyme immunoassay that could discriminate between HTLV-I and HTLV-II. Serum specimens from individuals whose infections were confirmed and typed by means of the polymerase chain reaction (PCR) were used to determine the sensitivity and specificity of the new assay. When 73 PCR-confirmed HTLV-I specimens were tested with the HTLV-I peptides, the absorbance values for 71 (97.3%) were at least two times higher than the values obtained with the HTLV-II peptides; these samples thus were classified as HTLV-I. Two specimens reacted with all the peptides and, therefore, could not be typed. Conversely, when 59 PCR-confirmed HTLV-II specimens were tested with the HTLV-II peptides, 55 (93%) produced high absorbance values and were typed as HTLV-II; 4 specimens could not be typed. None of the specimens was incorrectly typed; hence, the specificity of this assay was 100%. When this assay was compared with other HTLV immunoassays, the degrees of sensitivity and specificity were similar. The main advantage of this new assay is that synthetic peptides representing variant sequences can easily be added as new variant HTLV strains are identified.
机译:代表人T淋巴病毒I型(HTLV-1)(Env-1(191-214)和Env-5(242-257))和II(HTLV-II)包膜区域免疫优势结构基序的合成肽(Env-20(85-102和Env-2(187-209))用于开发可区分HTLV-I和HTLV-II的酶免疫分析方法。用聚合酶链反应(PCR)确定新方法的敏感性和特异性,当用HTLV-1肽对73份PCR确认的HTLV-1标本进行检测时,至少有71份(97.3%)的吸光度值反之,当59个经PCR确认的HTLV-II时,这些样品被归类为HTLV-I。两个样品与所有肽反应,因此无法分型。用HTLV-II肽测试了标本,有55个(93%)产生了高吸光度值,并被分类为HTLV-II。无法键入4个样本。没有一个标本输入错误;因此,该测定的特异性为100%。当将该测定法与其他HTLV免疫测定法进行比较时,敏感性和特异性程度相似。该新测定法的主要优点是,当鉴定出新的HTLV变异株时,可以轻松添加代表变异序列的合成肽。

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