Department of Microbiology, Faculty of Medicine, Kindai University, Osakasayama City 589-8511, Osaka, Japan.
Department of Internal Medicine, Japan Self Defense Forces Hanshin Hospital, Kawanishi City 666-0024, Hyogo, Japan.
Int J Mol Sci. 2023 Aug 18;24(16):12937. doi: 10.3390/ijms241612937.
Anti-glycolipid antibodies have been reported to play pathogenic roles in peripheral inflammatory neuropathies, such as Guillain-Barré syndrome. On the other hand, the role in multiple sclerosis (MS), inflammatory demyelinating disease in the central nervous system (CNS), is largely unknown, although the presence of anti-glycolipid antibodies was reported to differ among MS patients with relapsing-remitting (RR), primary progressive (PP), and secondary progressive (SP) disease courses. We investigated whether the induction of anti-glycolipid antibodies could differ among experimental MS models with distinct clinical courses, depending on induction methods. Using three mouse strains, SJL/J, C57BL/6, and A.SW mice, we induced five distinct experimental autoimmune encephalomyelitis (EAE) models with myelin oligodendrocyte glycoprotein (MOG), MOG, or myelin proteolipid protein (PLP), with or without an additional adjuvant curdlan injection. We also induced a viral model of MS, using Theiler's murine encephalomyelitis virus (TMEV). Each MS model had an RR, SP, PP, hyperacute, or chronic clinical course. Using the sera from the MS models, we quantified antibodies against 11 glycolipids: GM1, GM2, GM3, GM4, GD3, galactocerebroside, GD1a, GD1b, GT1b, GQ1b, and sulfatide. Among the MS models, we detected significant increases in four anti-glycolipid antibodies, GM1, GM3, GM4, and sulfatide, in PLP-induced EAE with an RR disease course. We also tested cellular immune responses to the glycolipids and found CD1d-independent lymphoproliferative responses only to sulfatide with decreased interleukin (IL)-10 production. Although these results implied that anti-glycolipid antibodies might play a role in remissions or relapses in RR-EAE, their functional roles need to be determined by mechanistic experiments, such as injections of monoclonal anti-glycolipid antibodies.
抗神经节苷脂抗体已被报道在周围炎性神经病中发挥致病作用,例如格林-巴利综合征。另一方面,在多发性硬化症(MS)中,中枢神经系统(CNS)的炎症性脱髓鞘疾病中的作用在很大程度上尚不清楚,尽管有报道称 MS 患者的复发缓解型(RR)、原发性进展型(PP)和继发性进展型(SP)疾病过程中存在抗神经节苷脂抗体的差异。我们研究了在具有不同临床病程的不同实验性 MS 模型中,根据诱导方法的不同,抗神经节苷脂抗体的诱导是否会有所不同。我们使用 SJL/J、C57BL/6 和 A.SW 三种小鼠品系,用髓鞘少突胶质细胞糖蛋白(MOG)、MOG 或髓鞘蛋白脂蛋白(PLP)诱导五种不同的实验性自身免疫性脑脊髓炎(EAE)模型,有或没有额外的佐剂凝乳酶注射。我们还使用 Theiler's 鼠脑脊髓炎病毒(TMEV)诱导了 MS 的病毒模型。每个 MS 模型都有 RR、SP、PP、超急性或慢性临床病程。使用 MS 模型的血清,我们定量了针对 11 种神经节苷脂的抗体:GM1、GM2、GM3、GM4、GD3、半乳糖脑苷脂、GD1a、GD1b、GT1b、GQ1b 和硫酸脑苷脂。在 MS 模型中,我们在 RR 疾病病程的 PLP 诱导的 EAE 中检测到四种抗神经节苷脂抗体 GM1、GM3、GM4 和硫酸脑苷脂的显著增加。我们还测试了对神经节苷脂的细胞免疫反应,发现仅对硫酸脑苷脂存在 CD1d 非依赖性淋巴增生反应,且白细胞介素(IL)-10 产生减少。尽管这些结果表明抗神经节苷脂抗体可能在 RR-EAE 的缓解或复发中发挥作用,但它们的功能作用需要通过机制实验来确定,例如注射单克隆抗神经节苷脂抗体。