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使用高输入量聚合酶链反应检测高危血清阴性个体中HIV-1 DNA的缺失情况

Absence of HIV-1 DNA in high-risk seronegative individuals using high-input polymerase chain reaction.

作者信息

Lee T H, el-Amad Z, Reis M, Adams M, Donegan E A, O'Brien T R, Moss A R, Busch M P

机构信息

Irwin Memorial Blood Centers, San Francisco, California 94118.

出版信息

AIDS. 1991 Oct;5(10):1201-7. doi: 10.1097/00002030-199110000-00008.

Abstract

Evidence of frequent HIV-1 infections in antibody-negative, high-risk individuals (so-called 'silent' infections) remains controversial. To evaluate whether these discrepant results may be the consequence of intermittent detection of rare infected cells (low viral load) preceding seroconversion, we developed a modification of the polymerase chain reaction (PCR) technique which enabled analysis of 10-fold greater amounts of cellular DNA per reaction than standard PCR (2 x 10(6) rather than 0.2 x 10(6) input cells). This technique allowed consistent detection of HIV-1 provirus in two seropositive individuals who had repeatedly tested negative by standard-input PCR. However, results were negative when high-input PCR was applied to 51 specimens from 39 selected high-risk seronegative individuals. These results suggest that variations in viral load preceding or in the absence of seroconversion probably do not explain discrepant evidence regarding silent HIV-1 infection.

摘要

在抗体阴性的高危个体中频繁出现HIV-1感染(即所谓的“隐匿性”感染)的证据仍存在争议。为了评估这些不一致的结果是否可能是血清转化前罕见感染细胞(低病毒载量)间歇性检测的结果,我们对聚合酶链反应(PCR)技术进行了改进,使得每个反应能够分析的细胞DNA量比标准PCR多10倍(输入细胞为2×10⁶个而非0.2×10⁶个)。该技术能够在两名经标准输入PCR反复检测呈阴性的血清阳性个体中持续检测到HIV-1前病毒。然而,当将高输入PCR应用于从39名选定的高危血清阴性个体中获取的51份样本时,结果均为阴性。这些结果表明,血清转化前或无血清转化时病毒载量的变化可能无法解释关于隐匿性HIV-1感染的不一致证据。

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