Department of Neurology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Neurology, the Affiliated Brain Hospital of Guangzhou Medical University, Guangzhou, China.
Front Immunol. 2019 Feb 6;10:103. doi: 10.3389/fimmu.2019.00103. eCollection 2019.
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is an autoimmune inflammatory brain disease that can develop a variety of neuropsychiatric presentations. However, the underlying nature of its inflammatory neuronal injury remains unclear. Mitochondrial DNA (mtDNA) is recently regarded as a damage-associated molecular pattern molecule (DAMP) that can initiate an inflammatory response. In the presenting study, we aimed to evaluate the levels of cell-free mtDNA in cerebrospinal fluid (CSF) of patients with anti-NMDAR encephalitis and to determine a potential role of cell-free mtDNA in the prognosis of anti-NMDAR encephalitis. A total of 33 patients with NMDAR encephalitis and 17 patients with other non-inflammatory disorders as controls were included in this study. The CSF levels of cell-free mtDNA were measured by quantitative polymerase chain reaction (qPCR). Cytokines including interleukin (IL)-6, IL-10, and tumor necrosis factor alpha (TNF-α) were measured by ELISA. The modified Rankin scale (mRS) score was evaluated for neurologic disabilities. Our data showed that the CSF levels of cell-free mtDNA and inflammation-associated cytokines were significantly higher in the patients with anti-NMDAR encephalitis compared with those in controls. Positive correlations were detected between the CSF levels of cell-free mtDNA and mRS scores of patients with anti-NMDAR encephalitis at both their admission and 6-month follow up. These findings suggest that the CSF level of cell-free mtDNA reflects the underlying neuroinflammatory process in patients with anti-NMDAR encephalitis and correlates with their clinical mRS scores. Therefore, cell-free mtDNA may be a potential prognostic biomarker for anti-NMDAR encephalitis.
抗 N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种自身免疫性炎症性脑病,可引起多种神经精神表现。然而,其炎症性神经元损伤的潜在性质尚不清楚。线粒体 DNA(mtDNA)最近被认为是一种损伤相关分子模式分子(DAMP),可引发炎症反应。在本研究中,我们旨在评估抗 NMDAR 脑炎患者脑脊液(CSF)中细胞游离 mtDNA 的水平,并确定细胞游离 mtDNA 在抗 NMDAR 脑炎预后中的潜在作用。本研究共纳入 33 例 NMDAR 脑炎患者和 17 例非炎症性疾病患者作为对照。通过定量聚合酶链反应(qPCR)测量细胞游离 mtDNA 的 CSF 水平。通过 ELISA 测量细胞因子,包括白细胞介素(IL)-6、IL-10 和肿瘤坏死因子-α(TNF-α)。通过改良 Rankin 量表(mRS)评分评估神经功能障碍。我们的数据显示,与对照组相比,抗 NMDAR 脑炎患者的 CSF 中细胞游离 mtDNA 和炎症相关细胞因子水平明显升高。在抗 NMDAR 脑炎患者的入院和 6 个月随访时,CSF 中细胞游离 mtDNA 水平与 mRS 评分呈正相关。这些发现表明,CSF 中细胞游离 mtDNA 水平反映了抗 NMDAR 脑炎患者潜在的神经炎症过程,并与他们的临床 mRS 评分相关。因此,细胞游离 mtDNA 可能是抗 NMDAR 脑炎的潜在预后生物标志物。