Shankar G, Cohen D A
Department of Microbiology and Immunology, University of Kentucky Chandler Medical Center, Lexington 40536-0084, USA.
J Immunoassay. 1997 Nov;18(4):371-88. doi: 10.1080/01971529708005828.
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.
一些细胞因子,如白细胞介素-4(IL-4)和白细胞介素-10(IL-10),其产生水平通常较低,采用标准酶联免疫吸附测定(ELISA)技术难以检测。在许多情况下,由于合成极少和/或细胞因子消耗,检测水平达到或接近该检测方法的灵敏度极限。为了提高对低水平检测到的细胞因子的定量,我们开发了一种独特的细胞培养捕获ELISA法。在24小时的体外激活期的最后6小时,将淋巴细胞在包被有抗细胞因子抗体的ELISA板中孵育。与传统ELISA技术相比,使用这种细胞培养捕获方法能持续提高几种T细胞细胞因子的检测水平。此外,发现该技术在不改变细胞培养捕获期之前细胞因子分泌速率的情况下提高了检测水平。因此,细胞培养捕获ELISA法可能有助于检测多种产生水平较低且传统上难以定量的细胞因子。