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免疫与转录组学方法研究干扰素-β1 和芬戈莫德治疗多发性硬化症患者时对自然杀伤细胞的差异化调节作用。

An immunological and transcriptomics approach on differential modulation of NK cells in multiple sclerosis patients under interferon-β1 and fingolimod therapy.

机构信息

Department of Neurology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.

Department of Basic Oncology, Hacettepe University Cancer Institute, Ankara, Turkey.

出版信息

J Neuroimmunol. 2020 Oct 15;347:577353. doi: 10.1016/j.jneuroim.2020.577353. Epub 2020 Jul 30.

Abstract

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.

摘要

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。

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