Istanbul University, Aziz Sancar Institute of Experimental Medicine, Department of Immunology, Istanbul, Turkey.
Koc University, Faculty of Medicine, Department of Neurology, Istanbul, Turkey; Istanbul University Cerrahpasa, Cerrahpasa Faculty of Medicine, Department of Neurology, Istanbul, Turkey.
Immunol Lett. 2019 Dec;216:63-69. doi: 10.1016/j.imlet.2019.10.006. Epub 2019 Oct 4.
Multiple Sclerosis (MS) is an immune-mediated and neurodegenerative disease of central nervous system. Relapsing-remitting (RR)-MS occurring with acute attacks and remissions, is the most common clinical type of MS. There are different strategies applied in first-line treatment of RR-MS patients such as interferon-beta (IFN-β) and glatiramer acetate. In this study, activating and inhibitory receptor expressions and interleukin (IL)-22 levels of NK cells were investigated in RR-MS patients with or without IFN-β therapy. Activating receptor expression and IL-22 levels of NK cells were increased in RR-MS patients under IFN-β therapy. Elevated NK cells with activating profile and increased IL-22 under IFN-β therapy suggest that IFN-β treatment might direct NK cells toward a pro-inflammatory status.
多发性硬化症(MS)是一种免疫介导和神经退行性疾病的中枢神经系统。复发缓解型(RR)MS 伴有急性发作和缓解,是 MS 最常见的临床类型。RR-MS 患者的一线治疗有不同的策略,如干扰素-β(IFN-β)和那他珠单抗。在这项研究中,研究了 RR-MS 患者是否接受 IFN-β 治疗,NK 细胞的激活和抑制受体表达以及白细胞介素(IL)-22 水平。RR-MS 患者在 IFN-β 治疗下,NK 细胞的激活受体表达和 IL-22 水平增加。IFN-β 治疗下 NK 细胞的表型激活和 IL-22 增加提示 IFN-β 治疗可能使 NK 细胞向促炎状态发展。