Department of Epileptology, Krankenhaus Mara, Bethel Epilepsy Center, Medical School OWL, Bielefeld University, Maraweg 21, 33617, Bielefeld, Germany.
Laboratory Krone, Bad Salzuflen, Germany.
J Neurol. 2024 Sep;271(9):6325-6335. doi: 10.1007/s00415-024-12594-9. Epub 2024 Aug 6.
Two-thirds of published patients with anti-leucine rich, glioma inactivated 1 (LGI1) encephalitis develop hippocampal sclerosis (HS). It is likely that this contributes to residual cognitive long-term deficits and the risk of epilepsy. Almost all patients harbor anti-LGI1-immunoglobulin G-(IgG-) subclass 4, which is considered a "benign", non-destructive subclass. In contrast, neuropathological case studies have suggested that the classical complement cascade may contribute to mediotemporal cell death in patients with LGI1 antibodies. IgG subclasses 1, 2, or 3 are required to initiate this cascade. We hypothesized that patients with these anti-LGI1-IgG1/2/3 in addition to IgG4 have a higher risk of developing HS than patients with anti-LGI1-IgG4 alone. We retrospectively assessed all anti-LGI1 encephalitis patients from this center with anti-LGI1-IgG-subclass information and follow-up MRI available. Nine out of 20 patients had developed HS (45%). Volumetric FreeSurfer analysis confirmed the visual HS diagnoses. HS and a lower hippocampal volume were associated with anti-LGI1-IgG1/2/3. All six patients with this IgG subclass status developed HS. There was no association with older or younger age at onset, female sex, longer latency from disease onset to start of immunotherapy, less intense immunotherapy, higher serum titers of LGI1 antibodies, LGI1 antibodies in CSF or higher LGI1-specific antibody indices. There was no association between anti-LGI1-IgG1/2/3 status and neuropsychological performance, epilepsy, or general neurological performance. This confirms our hypothesis that anti-LGI1-IgG1/2/3 in serum puts patients at risk of developing HS. If these findings can be confirmed and clinically corroborated, patients with anti-LGI1-IgG1/2/3 might become candidates for anti-complement-directed immunological treatments.
三分之二的抗亮氨酸丰富的神经胶质瘤失活 1 型(LGI1)脑炎患者出现海马硬化(HS)。这可能导致认知长期缺陷和癫痫风险增加。几乎所有患者都存在抗 LGI1-免疫球蛋白 G(IgG)-亚类 4,被认为是“良性”、非破坏性的亚类。相比之下,神经病理学病例研究表明,经典补体级联反应可能导致 LGI1 抗体患者的中颞细胞死亡。IgG 亚类 1、2 或 3 是启动此级联反应所必需的。我们假设,除了 IgG4 之外,具有这些抗 LGI1-IgG1/2/3 的患者比仅具有抗 LGI1-IgG4 的患者发生 HS 的风险更高。我们回顾性评估了该中心所有具有抗 LGI1-IgG 亚类信息和随访 MRI 可用的抗 LGI1 脑炎患者。20 名患者中有 9 名(45%)发展为 HS。FreeSurfer 体积分析证实了视觉 HS 诊断。HS 和海马体积减小与抗 LGI1-IgG1/2/3 相关。具有该 IgG 亚类状态的所有 6 名患者均发展为 HS。发病年龄、女性、从疾病发病到开始免疫治疗的潜伏期、免疫治疗强度、LGI1 抗体血清滴度、CSF 中的 LGI1 抗体或更高的 LGI1 特异性抗体指数与 HS 均无相关性。抗 LGI1-IgG1/2/3 状态与神经心理学表现、癫痫或一般神经表现之间无相关性。这证实了我们的假设,即血清中的抗 LGI1-IgG1/2/3 使患者有发展为 HS 的风险。如果这些发现可以得到证实并在临床上得到证实,那么具有抗 LGI1-IgG1/2/3 的患者可能成为抗补体导向免疫治疗的候选者。