Neier Steven C, Smith Stephen E P, Davis Tessa R, Gil Diana, Schrum Adam G
Department of Immunology, College of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
J Investig Dermatol Symp Proc. 2013 Dec;16(1):S31-3. doi: 10.1038/jidsymp.2013.9.
Development of better therapies for the T cell-mediated autoimmune disease alopecia areata (AA) could be expedited by an improved understanding of the immunologic signals underlying its pathogenesis. To approach this, our group is mounting a new technological and analytical platform, multiplex immunoprecipitation detected by flow cytometry (MIF). MIF is designed to allow analysis of collections of protein-protein interactions that participate in T cell signaling webs. Early experiments suggest that MIF can detect the increased protein-protein interaction network activity that occurs under conditions of T cell antigenic stimulation. Future experiments will focus on application of MIF to T cells isolated from AA or control patient samples, to identify critical T cell signaling complexes associated with the disorder.
通过更好地理解斑秃(AA)发病机制背后的免疫信号,可以加快针对T细胞介导的自身免疫性疾病斑秃的更好治疗方法的开发。为了实现这一点,我们的团队正在搭建一个新的技术和分析平台,即流式细胞术检测的多重免疫沉淀(MIF)。MIF旨在分析参与T细胞信号网络的蛋白质-蛋白质相互作用集合。早期实验表明,MIF可以检测在T细胞抗原刺激条件下发生的蛋白质-蛋白质相互作用网络活性增加。未来的实验将集中于将MIF应用于从AA患者或对照患者样本中分离出的T细胞,以识别与该疾病相关的关键T细胞信号复合物。