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伊朗东北部马什哈德地区采用巢式 PCR 法对免疫印迹不确定样本进行 HTLV-II 感染检测的结果

No Evidence of HTLV-II Infection Among Immonoblot Indeterminate Samples Using Nested PCR in Mashhad, Northeast of Iran.

机构信息

Research Centre for HIV/AIDS, HTLV and Viral Hepatitis, Iranian Academic Centre for Education, Culture & Research (ACECR), Mashhad Branch, Mashhad, Iran ; Inflammation and Inflammatory Diseases Research Centre, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.

Research Centre for HIV/AIDS, HTLV and Viral Hepatitis, Iranian Academic Centre for Education, Culture & Research (ACECR), Mashhad Branch, Mashhad, Iran.

出版信息

Iran J Basic Med Sci. 2013 Mar;16(3):229-34.

PMID:24470868
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3881255/
Abstract

OBJECTIVE(S): Although HTLV-I infection is endemic in different geographical parts of the world including Northeast of Iran, there have been no documents of HTLV-II infection in this region. It is reported that one possible reason for seroindeterminate state in HTLV western blot is HTLV-II virus. This study aimed to investigate the presence of HTLV-II among blood donors with seroindeterminate western blot results.

MATERIALS AND METHODS

Three ml whole blood obtained from 50 blood donors referring to Mashhad Blood Transfusion Organization who had reactive Elisa for HTLV-I and seroindeterminate HTLV western blot state. A conventional PCR was applied to detect HTLV-I provirus using specific primers while a nested PCR was designed with specific external and internal primers for the detection of HTLV-II.

RESULTS

The average age of participants, 39 males and 11 females, was 37.12± 14.36 years. The average OD of the Elisa assay was 1.767± 1.195. The most common indeterminate patterns were Rgp46-II alone (n=12, 27.3%), Rgp46-I alone (n=7, 15.9%), and Rgp46-I with GD21 (n=7, 15.9%).After introducing the DNA to the PCR tests, results revealed 10 (20%) HTLV-I PCR positive samples while no HTLV-II positive sample was detected by nested PCR. There were no significant age, blood group, Optical Density of the Elisa assay, and western blot indeterminate pattern differences between HTLV-I PCR positive and negative samples. Conclusion : No HTLV-II positive sample was detected in this study which confirms the absence of HTLV-II infection in this region. However, high frequency of HTLV-I PCR positive samples among the seroindeterminate cases implies on the important role of molecular techniques for further confirmation of the infection.

摘要

目的

尽管 HTLV-I 感染在包括伊朗东北部在内的世界不同地理区域流行,但该地区尚未有 HTLV-II 感染的记录。据报道,HTLV 免疫印迹出现血清不确定状态的一个可能原因是 HTLV-II 病毒。本研究旨在调查血清学不确定的 HTLV 免疫印迹结果的献血者中是否存在 HTLV-II。

材料和方法

从马什哈德血液中心的 50 名 HTLV-I 酶联免疫吸附试验(ELISA)阳性且 HTLV 免疫印迹血清不确定的献血者中采集 3ml 全血。使用特异性引物的常规聚合酶链反应(PCR)用于检测 HTLV-I 前病毒,而设计了巢式 PCR 以使用特异性外部和内部引物检测 HTLV-II。

结果

39 名男性和 11 名女性参与者的平均年龄为 37.12±14.36 岁。ELISA 检测的平均 OD 值为 1.767±1.195。最常见的不确定模式是单独的 Rgp46-II(n=12,27.3%)、单独的 Rgp46-I(n=7,15.9%)和 Rgp46-I 与 GD21(n=7,15.9%)。将 DNA 引入 PCR 检测后,结果显示 10(20%)例 HTLV-I PCR 阳性样本,而巢式 PCR 未检测到 HTLV-II 阳性样本。HTLV-I PCR 阳性和阴性样本之间在年龄、血型、ELISA 检测的光密度和免疫印迹不确定模式方面无显著差异。结论:本研究未检测到 HTLV-II 阳性样本,证实该地区不存在 HTLV-II 感染。然而,血清学不确定病例中 HTLV-I PCR 阳性样本的高频率表明分子技术对于进一步确认感染具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1838/3881255/f8a23ffc208e/ijbms-16-229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1838/3881255/f8a23ffc208e/ijbms-16-229-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1838/3881255/f8a23ffc208e/ijbms-16-229-g001.jpg

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