Department of Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Department of Basic Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.
J Neuroimmunol. 2020 Oct 15;347:577353. doi: 10.1016/j.jneuroim.2020.577353. Epub 2020 Jul 30.
This study aims to compare NK cells obtained from multiple sclerosis (MS) patients receiving interferon-β1 and fingolimod therapies. Fingolimod reduced the CD56 NK cell subset. The remaining CD56 NK cells displayed NKG2D, NKp46, CD107a, and IFN-γ levels similar to those from the patients under interferon-β1 therapy. Alternatively, comparative transcriptomics and pathway analyses revealed significant distinctions between two therapy modalities. Molecular signature of the CD56 NK cells from fingolimod-treated MS patients was closely associated to those from healthy subjects. The basic assets of NK cells were modestly influenced by interferon-β1 and fingolimod, however transcriptomics showed profound alterations in NK responses.
本研究旨在比较接受干扰素-β1 和芬戈莫德治疗的多发性硬化症 (MS) 患者的 NK 细胞。芬戈莫德减少了 CD56 NK 细胞亚群。剩余的 CD56 NK 细胞显示出与接受干扰素-β1 治疗的患者相似的 NKG2D、NKp46、CD107a 和 IFN-γ 水平。或者,比较转录组学和通路分析揭示了两种治疗方式之间的显著差异。来自接受芬戈莫德治疗的 MS 患者的 CD56 NK 细胞的分子特征与健康受试者的分子特征密切相关。NK 细胞的基本特征受到干扰素-β1 和芬戈莫德的轻微影响,但是转录组学显示 NK 反应发生了深刻的改变。