Wang Yuge, Zhou Yifan, Sun Xiaobo, Lu Tingting, Wei Lei, Fang Ling, Chen Chen, Huang Qiao, Hu Xueqiang, Lu Zhengqi, Peng Lisheng, Qiu Wei
Department of Neurology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Neuroimmunomodulation. 2016;23(5-6):352-358. doi: 10.1159/000464135. Epub 2017 Apr 27.
To screen cytokines and chemokines and determine their dynamic changes in the serum and cerebrospinal fluid (CSF) of patients with neuromyelitis optica spectrum disorder (NMOSD).
Eight NMOSD with seropositive aquaporin-4 antibody (AQP4-IgG) were enrolled, as well as 8 matched patients with multiple sclerosis (MS) and 8 with noninflammatory neurological diseases, who were included as controls. In total, 102 cytokines and 34 chemokines were detected in the CSF and serum of NMOSD patients and controls.
CSF interleukin (IL)-17A levels were significantly higher in NMOSD patients in the relapsing phase (27.15 ± 11.33) than in those in the remitting phase (10.04 ± 3.11, p = 0.0017), and patients with MS (14.72 ± 3.20, p = 0.0283) and other controls (10.39 ± 11.38, p = 0.0021). CSF IL-6 levels were higher in the NMOSD patients in the relapsing phase (12.23 ± 3.47) than in those in the remitting phase (5.87 ± 2.78, p = 0.0001), and MS patients (7.38 ± 2.35, p = 0.0033) and other controls (7.50 ± 0.37, p = 0.0043). CSF CCL19 levels were also significantly higher in NMOSD patients in the relapsing phase (35.87 ± 27.07) than in those in the remitting phase (10.71 ± 3.62, p = 0.0215). Serum IL-19 levels were lower in NMOSD patients in the relapsing phase (6.23 ± 1.95) than in those in the remitting phase (10.72 ± 4.46, p = 0.0092). Further, there was a positive, significant correlation between serum IL-9 concentration and the Expanded Disability Status Scale score in the NMOSD patients in the relapsing phase (p = 0.04).
In addition to IL-6 and IL-17A, IL-16 and CCL19 act as proinflammatory cytokines/chemokines, while IL-19 plays a protective role in NMOSD pathogenesis.
筛选视神经脊髓炎谱系障碍(NMOSD)患者血清和脑脊液(CSF)中的细胞因子和趋化因子,并确定其动态变化。
纳入8例水通道蛋白4抗体(AQP4-IgG)血清阳性的NMOSD患者,以及8例匹配的多发性硬化(MS)患者和8例非炎性神经系统疾病患者作为对照。共检测了NMOSD患者和对照者脑脊液和血清中的102种细胞因子和34种趋化因子。
复发期NMOSD患者脑脊液白细胞介素(IL)-17A水平(27.15±11.33)显著高于缓解期患者(10.04±3.11,p = 0.0017),也高于MS患者(14.72±3.20,p = 0.0283)和其他对照者(10.39±11.38,p = 0.0021)。复发期NMOSD患者脑脊液IL-6水平(12.23±3.47)高于缓解期患者(5.87±2.78,p = 0.0001),也高于MS患者(7.38±2.35,p = 0.0033)和其他对照者(7.50±0.37,p = 0.0043)。复发期NMOSD患者脑脊液CCL-19水平(35.87±27.07)也显著高于缓解期患者(10.71±3.62,p = 0.0215)。复发期NMOSD患者血清IL-十九水平(6.23±1.95)低于缓解期患者(10.72±4.46,p = 0.0092)。此外,复发期NMOSD患者血清IL-9浓度与扩展残疾状态量表评分之间存在显著正相关(p = 0.04)。
除IL-6和IL-17A外,IL-16和CCL19作为促炎细胞因子/趋化因子发挥作用,而IL-19在NMOSD发病机制中起保护作用。