Amplification of Complete HIV-1 Envelope Genes from Purified CD4+ T Cell Populations

Y. Jiao, Juan Li, Wei Hua, Yanqing Gao, Tong Zhang, Hao Wu
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Abstract

Polymerase chain reaction (PCR) amplification of full-length HIV-1 envelope genes directly from uncultured clinical samples or from plasma of HIV patients using RT-PCR or from peripheral blood mononuclear cells (PBMC) DNA extracts of HIV patients is difficult. As HIV mainly infected CD4 positive cells, this paper first describes a sensitive method for the amplification of full-length HIV-1 envelope genes from purified CD4+ cells, and compares this method with other, less effective, procedures. This method were suitable for amplification of HIV-1 envelope genes directly from clinical samples especially from those of low viral load.
纯化CD4+ T细胞群中HIV-1包膜基因的扩增
用RT-PCR直接从未培养的临床样本或HIV患者血浆或HIV患者外周血单个核细胞(PBMC) DNA提取物中扩增全长HIV-1包膜基因是困难的。由于HIV主要感染CD4阳性细胞,本文首先描述了一种从纯化的CD4+细胞中扩增全长HIV-1包膜基因的灵敏方法,并与其他效率较低的方法进行了比较。该方法适用于直接从临床样品中扩增HIV-1包膜基因,特别是从低病毒载量的样品中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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