Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
Institute for Multiple Sclerosis Research and Neuroimmunology, University Medical Centre Göttingen, Göttingen, Germany.
Front Immunol. 2018 May 16;9:1060. doi: 10.3389/fimmu.2018.01060. eCollection 2018.
Compared to naive T cells, differentiated T cells are thought to be less dependent on CD28 costimulation for full activation. To revisit the role of CD28 costimulation in mouse T cell recall responses, we adoptively transferred generated OT-II T helper (Th) 1 cells into C57BL/6 mice (Thy1.2) and then either blocked CD28-ligand interactions with Fab fragments of the anti-CD28 monoclonal antibody (mAb) E18 or deleted CD28 expression using inducible CD28 knock-out OT-II mice as T cell donors. After injection of ovalbumin protein in adjuvant into the recipient mice we observed that systemic interferon (IFN)γ release strongly depended on CD28 costimulation of the Th1 cells, while secondary clonal expansion was not reduced in the absence of CD28 costimulation. For human memory CD4 T cell responses we also noted that cytokine release was reduced upon inhibition of CD28 costimulation. Together, our data highlight the so far underestimated role of CD28 costimulation for the reactivation of fully differentiated CD4 T cells.
与幼稚 T 细胞相比,分化的 T 细胞被认为对 CD28 共刺激的依赖性较低,以实现完全激活。为了重新审视 CD28 共刺激在小鼠 T 细胞回忆反应中的作用,我们将生成的 OT-II T 辅助(Th)1 细胞过继转移到 C57BL/6 小鼠(Thy1.2)中,然后用抗 CD28 单克隆抗体(mAb)E18 的 Fab 片段阻断 CD28-配体相互作用,或使用诱导型 CD28 敲除 OT-II 小鼠作为 T 细胞供体来删除 CD28 表达。在给受体小鼠注射佐剂中的卵清蛋白蛋白后,我们观察到系统干扰素(IFN)γ释放强烈依赖于 Th1 细胞的 CD28 共刺激,而在缺乏 CD28 共刺激的情况下,二次克隆扩增并未减少。对于人类记忆 CD4 T 细胞反应,我们还注意到,抑制 CD28 共刺激会减少细胞因子的释放。总之,我们的数据强调了 CD28 共刺激在完全分化的 CD4 T 细胞再激活中的作用,这一作用迄今为止被低估了。