多发性硬化
外周血单个核细胞
促炎细胞因子
生物标志物
免疫学
医学
内科学
半胱氨酸蛋白酶1
半胱氨酸蛋白酶3
细胞外
白细胞介素
细胞因子
细胞凋亡
炎症
生物
炎症体
程序性细胞死亡
细胞生物学
体外
生物化学
作者
Masoumeh Beheshti,Zahra Salehi,Roya Abolfazli,Hedayatolah Shirzad,Maryam Izad
标识
DOI:10.18502/ijaai.v19i5.4470
摘要
Multiple sclerosis (MS) is an inflammatory autoimmune disease of the central nervous system, in which proinflammatory cytokines play a critical role in the pathogenic formation of lesions. Caspase-1 is a cysteine protease that proteolytically cleaves precursors of interleukin (IL)-18 and IL-1β and turns them into their active forms. These inflammatory cytokines play an important role in the development of MS. The aim of the present study was the investigation of caspase-1 and its downstream products, IL-18 and IL-1β, in relapsing-remitting MS (RRMS) patients. In this study, we used an ELISA assay to measure serum and cellular caspase-1 and serum levels of IL-18 and IL-1β in RRMS patients in the relapse phase (n=23) and healthy age-and gender-matched controls (n=19). We observed that the caspase-1 level was significantly increased in the serum of MS patients compared to the healthy controls (p=0.03). Although caspase-1 concentration in the lysate of peripheral blood mononuclear cells (PBMCs) was higher than serum among patients and controls (p<0.001), no significant difference was found in cellular levels of caspase-1 between the two groups. There was no significant difference in serum levels of IL-18 and IL-1β between patients and controls. In this study, we found an elevation of extracellular caspase-1, as a reflection of its intracellular level, in the serum of RRMS patients during the relapse phase. Therefore, it suggests being a suitable peripheral biomarker of disease activity in multiple sclerosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI