基于细胞培养的新型ELISA增强细胞因子检测。

G Shankar, D A Cohen
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引用次数: 11

摘要

一些细胞因子的产生,如IL-4和IL-10,通常发生在低水平,很难用标准的ELISA技术检测。在许多情况下,由于合成和/或细胞因子消耗最小,检测水平达到或接近测定的灵敏度极限。为了提高弱检测细胞因子的定量,我们开发了一种独特的细胞培养捕获ELISA。淋巴细胞在抗细胞因子抗体包被的ELISA板中孵育24小时体外活化期的最后6小时。与传统的ELISA技术相比,使用这种细胞培养捕获方法一致地增强了几种T细胞因子的检测。此外,该技术被发现在不改变细胞培养捕获期之前发生的细胞因子分泌率的情况下增强了检测。因此,细胞培养捕获ELISA可用于检测各种低水平产生的细胞因子,并且传统上难以量化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced cytokine detection by a novel cell culture-based ELISA.

Production of some cytokines, such as IL-4 and IL-10, often occurs at low levels and is difficult to detect by standard ELISA techniques. In many cases the level of detection is at or near to the limits of sensitivity of the assay due either to minimal synthesis and/or cytokine consumption. In an effort to enhance the quantitation of weakly detected cytokines we have developed a unique cell culture-capture ELISA. Lymphocytes are incubated in an anti-cytokine antibody coated ELISA plate for the last 6 hours of a 24 hour in vitro activation period. Use of this cell culture capture method consistently enhanced detection of several T cell cytokines compared to conventional ELISA techniques. Moreover, this technique was found to enhance detection without altering the rate of cytokine secretion which occurred prior to the cell culture capture period. Thus, the cell culture capture ELISA may be useful for detection of a variety of cytokines which are produced at low levels and have traditionally been difficult to quantify.

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