Rebhahn Jonathan A, Bishop Courtney, Divekar Anagha A, Jiminez-Garcia Katty, Kobie James J, Lee F Eun-Hyung, Maupin Genny M, Snyder-Cappione Jennifer E, Zaiss Dietmar M, Mosmann Tim R
David H. Smith Center for Vaccine Biology and Immunology, University of Rochester, Rochester, NY 14642, USA.
Comput Methods Programs Biomed. 2008 Oct;92(1):54-65. doi: 10.1016/j.cmpb.2008.06.002. Epub 2008 Jul 21.
The Elispot effectively measures the frequencies of cells secreting particular molecules, especially low-frequency cells such as antigen-specific T cells. The Fluorospot assay adapted this analysis to two products per cell, and this has now been extended to three-color measurement of both mouse and human cytokine-secreting cells. Due to the increased data complexity, and particularly the need to define single-, double- and triple-producing cells, it is critical to objectively quantify spot number, size, intensity, and coincidence with other spots. An automated counting program, Exploraspot, was therefore developed to detect and quantify Fluorospots in automated fluorescence microscope images. Morphological parameters, including size, intensity, location, circularity and others are calculated for each spot, exported in FCS format, and further analyzed by gating and graphical display in popular flow cytometry analysis programs. The utility of Exploraspot is demonstrated by identification of single-, double- and triple-secreting T cells; tolerance of variable background fluorescence; and estimation of the numbers of genuine versus random multiple events.
酶联免疫斑点技术(Elispot)能有效测量分泌特定分子的细胞频率,尤其是低频细胞,如抗原特异性T细胞。荧光免疫斑点分析(Fluorospot)将这种分析方法应用于每个细胞分泌两种产物的情况,现在已扩展到对小鼠和人类细胞因子分泌细胞进行三色测量。由于数据复杂性增加,特别是需要定义单分泌、双分泌和三分泌细胞,客观量化斑点数量、大小、强度以及与其他斑点的重合情况至关重要。因此,开发了一种自动计数程序Exploraspot,用于在自动荧光显微镜图像中检测和量化Fluorospot斑点。为每个斑点计算包括大小、强度、位置、圆形度等在内的形态学参数,以FCS格式导出,并在流行的流式细胞术分析程序中通过设门和图形显示进行进一步分析。通过识别单分泌、双分泌和三分泌T细胞、对可变背景荧光的耐受性以及对真实与随机多重事件数量的估计,证明了Exploraspot的实用性。