Versteegen J M, Logtenberg T, Ballieux R E
Department of Clinical Immunology, University Hospital, Utrecht, The Netherlands.
J Immunol Methods. 1988 Jun 28;111(1):25-9. doi: 10.1016/0022-1759(88)90055-5.
We present a method to detect and enumerate individual interferon (IFN)-producing human lymphocytes. The assay is based on the ELISA-plaque assay developed by Sedgwick and Holt (J. Exp. Med. (1983) 157, 2178; J. Immunol. Methods (1986) 87, 37). Mitogen-stimulated T cells are seeded in anti-IFN-gamma-coated wells. After a 16 h incubation period, the cells are removed. Subsequently a rabbit anti-IFN-gamma-antiserum followed by goat anti-rabbit antiserum conjugated to alkaline phosphatase are used to detect the IFN-gamma spots. Application of the spot-ELISA in combination with the conventional ELISA reveals the amount of IFN-gamma produced per cell. The spot-ELISA is a highly sensitive, easy to perform and rapid assay. Provided specific antisera are available, this method is suitable to detect production of other lymphokines at the single-cell level. To our knowledge, this is the first report of a single, well-defined T cell product measurement by the spot-ELISA.
我们提出了一种检测和计数产生干扰素(IFN)的单个人类淋巴细胞的方法。该检测方法基于Sedgwick和Holt开发的ELISA蚀斑检测法(《实验医学杂志》(1983年)157卷,2178页;《免疫方法学杂志》(1986年)87卷,37页)。将丝裂原刺激的T细胞接种在包被有抗IFN-γ的孔中。孵育16小时后,去除细胞。随后,使用兔抗IFN-γ抗血清,接着是与碱性磷酸酶偶联的山羊抗兔抗血清来检测IFN-γ斑点。斑点ELISA与传统ELISA相结合可揭示每个细胞产生的IFN-γ量。斑点ELISA是一种高度灵敏、易于操作且快速的检测方法。如果有特异性抗血清,该方法适用于在单细胞水平检测其他淋巴因子的产生。据我们所知,这是首次通过斑点ELISA对单一、明确的T细胞产物进行测量的报告。