Mostaghimi Darius, Mehta Sameet, Yoon Jennifer, Kosana Priya, Marra Christina M, Corley Michael J, Farhadian Shelli F
Section of Infectious Diseases, Yale School of Medicine, New Haven, Connecticut.
Department of Genetics, Yale School of Medicine, New Haven, Connecticut.
J Infect Dis. 2025 Apr 15;231(4):883-893. doi: 10.1093/infdis/jiae476.
Epigenetic changes within immune cells may contribute to neuroinflammation during bacterial infection, but their role in neurosyphilis (NS) pathogenesis and response has not yet been established. We longitudinally analyzed DNA methylation and RNA expression in cerebrospinal fluid (CSF) cells and peripheral blood mononuclear cells (PBMCs) from 11 participants with laboratory-confirmed NS (CSF Venereal Disease Research Laboratory test positive) and 11 matched controls with syphilis without NS (non-NS). DNA methylation profiles from CSF and PBMCs of participants with NS significantly differed from those of participants with non-NS. Some genes associated with these differentially methylated sites had corresponding RNA expression changes in the CSF (111/1097 [10.1%]), and included genes involved in B cell activation and insulin-response pathways. Despite antibiotic treatment, approximately 80% of CSF methylation changes associated with NS persisted, suggesting that epigenetic scars accompanying NS may persistently affect immunity following infection. Future studies must examine whether these sequelae are clinically meaningful.
免疫细胞内的表观遗传变化可能在细菌感染期间导致神经炎症,但其在神经梅毒(NS)发病机制和反应中的作用尚未明确。我们纵向分析了11例实验室确诊为NS(脑脊液性病研究实验室试验呈阳性)的参与者以及11例匹配的无NS梅毒患者(非NS)的脑脊液(CSF)细胞和外周血单核细胞(PBMC)中的DNA甲基化和RNA表达情况。NS参与者的CSF和PBMC的DNA甲基化谱与非NS参与者的显著不同。与这些差异甲基化位点相关的一些基因在CSF中具有相应的RNA表达变化(111/1097 [10.1%]),包括参与B细胞活化和胰岛素反应途径的基因。尽管进行了抗生素治疗,但与NS相关的CSF甲基化变化中约80%仍然存在,这表明伴随NS的表观遗传疤痕可能在感染后持续影响免疫力。未来的研究必须检验这些后遗症是否具有临床意义。