Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, United States.
Department of Medical Microbiology and Immunology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, United States.
Front Immunol. 2019 Jul 24;10:1553. doi: 10.3389/fimmu.2019.01553. eCollection 2019.
The presence of autoantibodies against 14-3-3ζ in human autoimmune diseases indicates its antigenic function. However, neither the cause nor the consequence of this newly-identified antigenic function of 14-3-3ζ protein is known. To address this, we investigated the immunological functions of 14-3-3ζ by studying effects on human peripheral blood mononuclear cells (PBMC) proliferation, polarization, and cytokine production. Exogenous 14-3-3ζ promoted PBMC proliferation and T cell polarization toward Th1 and Th17 populations. Significant increases in IFN-γ and IL-17 levels were observed in the presence of 14-3-3ζ. A specific increase in Th1 cells and IFN-γ production provided strong evidence for MHC class II presentation of 14-3-3ζ antigen. Particularly HLA-DRB10401 allele strongly promoted 14-3-3ζ-induced IFN-γ producing cells. In contrast, prednisolone treatment suppressed both 14-3-3ζ-induced T cell polarization and cytokine production. Overall, we show that MHC presentation and the adaptor functions of 14-3-3ζ participate in promoting IFN-γ and IL-17 production, two of the cytokines commonly associated with autoimmune diseases. To the best of our knowledge, this is the first report describing the antigenic function of 14-3-3ζ with human PBMC, thereby providing the basis of its immunological role in human diseases.
自身抗体针对人类自身免疫性疾病中的 14-3-3ζ 的存在表明了其抗原功能。然而,这种新确定的 14-3-3ζ 蛋白的抗原功能的原因和后果都尚不清楚。为了解决这个问题,我们通过研究对人外周血单核细胞(PBMC)增殖、极化和细胞因子产生的影响来研究 14-3-3ζ 的免疫功能。外源性 14-3-3ζ 促进 PBMC 增殖和 T 细胞向 Th1 和 Th17 群体的极化。在存在 14-3-3ζ 的情况下,观察到 IFN-γ 和 IL-17 水平的显著增加。Th1 细胞和 IFN-γ 产生的特异性增加为 14-3-3ζ 抗原的 MHC Ⅱ类呈递提供了有力证据。特别是 HLA-DRB10401 等位基因强烈促进 14-3-3ζ 诱导的 IFN-γ 产生细胞。相比之下,泼尼松龙治疗抑制了 14-3-3ζ 诱导的 T 细胞极化和细胞因子产生。总的来说,我们表明 MHC 呈递和 14-3-3ζ 的衔接功能参与促进 IFN-γ 和 IL-17 的产生,这两种细胞因子通常与自身免疫性疾病有关。据我们所知,这是首次描述 14-3-3ζ 与人类 PBMC 的抗原功能的报告,从而为其在人类疾病中的免疫作用提供了基础。