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用于检测母血中胎儿红细胞的罕见事件分析方法。

Rare-event analysis methods for detection of fetal red blood cells in maternal blood.

作者信息

Cupp J E, Leary J F, Cernichiari E, Wood J C, Doherty R A

出版信息

Cytometry. 1984 Mar;5(2):138-44. doi: 10.1002/cyto.990050207.

Abstract

Methods for analyzing very small subpopulations of cells ("rare-event analysis methods") are of interest in many areas of biology. In this paper we demonstrate the ability to detect one Rh-positive erythrocyte per 100,000 Rh-negative erythrocytes. This is the level needed to detect human fetal red blood cells in the maternal circulation in the case of fetal-maternal Rh-incompatibility. Erythrocytes stained with fluorescent immunobeads are more than 100 times as bright as the same cells stained by indirect immunofluorescence (or almost 40 times as bright as cells stained by the biotin-avidin technique). More importantly there is greater than a sevenfold increase in signal-to-noise (S/N) ratio, which proves critical in detecting very low frequency ("rare event") cell subpopulations. Although equal mixtures of positive and negative cells can easily be detected, positives cannot be easily distinguished from negatives when they are present in relative frequencies of 1:1000 or less as measured by either indirect immunofluorescence or biotin-fluorescent avidin labeling of D antigens. However, use of fluorescent immunobeads and high-speed flow cytometry allows detection of subpopulations of the same cells at relative frequencies of less than 1:100,000. Based on calibrations using free-fluorescent immunobeads, the average Rh-positive cell (when present in a relative frequency of 1:100,000) labeled with 36 +/- 19 fluorescent immunobeads. Rh-positive cells of relative frequencies 1:10,000 and 1:100,000 can be detected above background (Rh-negative red blood cells treated with the same amount of fluorescent immunobeads). Using defined mixtures of Rh-positive and negative cells, the expected numbers of positive cells were observed over a range of 1:100 to 1:100,000 relative Rh-positive cell frequencies. These methods should prove of general use in applications where original frequency information about rare cell subpopulations is important and would be lost if enrichment procedures were to be used.

摘要

分析极少量细胞亚群的方法(“稀有事件分析方法”)在生物学的许多领域都备受关注。在本文中,我们展示了每100,000个Rh阴性红细胞中检测出一个Rh阳性红细胞的能力。这是在母婴Rh血型不相容情况下,检测母体循环中胎儿红细胞所需的水平。用荧光免疫微珠染色的红细胞比用间接免疫荧光染色的相同细胞亮100多倍(或比用生物素-抗生物素蛋白技术染色的细胞亮近40倍)。更重要的是,信噪比(S/N)提高了七倍多,这在检测极低频率(“稀有事件”)细胞亚群时至关重要。虽然阳性和阴性细胞的等量混合物很容易被检测到,但当通过间接免疫荧光或D抗原的生物素-荧光抗生物素蛋白标记测量时,阳性细胞以1:1000或更低的相对频率存在时,阳性细胞与阴性细胞很难区分。然而,使用荧光免疫微珠和高速流式细胞术可以检测相对频率低于1:100,000的相同细胞亚群。基于使用游离荧光免疫微珠的校准,平均每个Rh阳性细胞(当相对频率为1:100,000时)标记有36±19个荧光免疫微珠。相对频率为1:10,000和1:100,000的Rh阳性细胞可以在背景(用相同数量荧光免疫微珠处理的Rh阴性红细胞)之上被检测到。使用定义的Rh阳性和阴性细胞混合物,在1:100至1:100,000的相对Rh阳性细胞频率范围内观察到了预期数量的阳性细胞。这些方法在稀有细胞亚群的原始频率信息很重要且如果使用富集程序就会丢失的应用中应具有普遍用途。

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