Poznansky M C, Walker B, Haseltine W A, Sodroski J, Langhoff E
Dana Farber Cancer Institute, Department of Pathology, Harvard Medical School, Boston, MA 02115.
J Acquir Immune Defic Syndr (1988). 1991;4(4):368-73.
This article describes a novel approach to quantitative polymerase chain reactions (PCR). The technique is simple to execute, can be performed in a single tube, and is suitable for automation. In addition, the counting and lysis of low numbers of cells (1-100) can be confirmed by phase contrast microscopy. In this study, the technique was used to determine the frequency of occurrence of DNA from the human immunodeficiency virus (type 1) in leukocyte subsets of peripheral blood mononuclear cells (PBMC) from sero-positive individuals. It was confirmed that the frequency of infected CD4+ T cells varied from 0.01 to 0.0001. In addition, HIV-1 DNA was detected in the B cell/dendritic cell-enriched subpopulation in four of nine HIV-1-positive individuals in the study.
本文介绍了一种定量聚合酶链反应(PCR)的新方法。该技术操作简单,可在单个试管中进行,且适合自动化操作。此外,通过相差显微镜可以确认少量细胞(1 - 100个)的计数和裂解情况。在本研究中,该技术用于测定血清阳性个体外周血单个核细胞(PBMC)白细胞亚群中人类免疫缺陷病毒(1型)DNA的出现频率。已证实受感染的CD4 + T细胞频率在0.01至0.0001之间变化。此外,在该研究的9名HIV - 1阳性个体中的4名个体的富含B细胞/树突状细胞的亚群中检测到了HIV - 1 DNA。