Pisa Marco, Croese Tommaso, Costa Gloria Dalla, Congiu Martina, Gelibter Stefano, Orrico Mario, Moiola Lucia, Comi Giancarlo, Furlan Roberto, Leocani Letizia
Vita-Salute San Raffaele University, Milan, Italy.
Experimental Neurophysiology Unit, Institute of Experimental Neurology (INSPE), IRCCS San Raffaele Scientific Institute, Milan, Italy.
Neurol Sci. 2025 May 21. doi: 10.1007/s10072-025-08198-4.
Natalizumab is a potent treatment for multiple sclerosis (MS). By inhibiting immune cell trafficking to the CNS it increases the risk of progressive multifocal leukoencephalopathy (PML). Extended interval dosing (EID) aims to mitigate PML risk by partly restoring immune surveillance. End-of-dose symptoms, frequently reported by people on EID, may reflect an increased inflammatory cell trafficking.
Twenty-five clinically and radiographically stable individuals on EID underwent neuropsychological (processing speed - PASAT and SDMT; self-reported fatigue - FSS), neurophysiological (SICI - Short Intracortical Inhibition, ICF- Intracortical facilitation, and CSP- cortical silent period), immunological assessments (circulating lymphocytes subpopulations and cytokines production), and plasma neurofilament quantification at the 2nd-4th and 6th-8th week after infusion.
24/25 participants subjectively reported increased fatigue at the end-of-dose; no change in processing speed or self-reported fatigue was detected. At the end-of-dose, a selective drop in IFN𝛾-producing lymphocytes (CD4+: -57.7%, p = 0.01; CD8+: -41.45%, p = 0.014; NK: -54.23%, p = 0.033) and other pro-inflammatory lymphocyte subsets was observed compared with the intermediate visit. Furthermore, we observed changes in GABAergic cortical excitability, with an increased GABA-A dependent inhibition of the primary motor cortex at the end-of-dose (SICI, + 46.9%, p = 0.026) and a similar trend for GABA-B depended inhibition (CSP). Plasma neurofilament fluctuations were below the study's detection power.
Pro-inflammatory lymphocytes escape peripheral circulation at the end-of-dose, in the absence of clinical or radiographic disease activity. The observed change in GABA-dependent cortical inhibition may reflect this increased CNS lymphocyte trafficking. No association with end-of-dose symptoms was found.
那他珠单抗是治疗多发性硬化症(MS)的有效药物。通过抑制免疫细胞向中枢神经系统的转运,它增加了进行性多灶性白质脑病(PML)的风险。延长给药间隔(EID)旨在通过部分恢复免疫监测来降低PML风险。EID患者经常报告的给药末期症状可能反映了炎症细胞转运增加。
25名临床和影像学稳定的EID患者在输注后第2 - 4周和第6 - 8周接受了神经心理学评估(处理速度 - PASAT和SDMT;自我报告的疲劳 - FSS)、神经生理学评估(短皮质内抑制 - SICI、皮质内易化 - ICF和皮质静息期 - CSP)、免疫学评估(循环淋巴细胞亚群和细胞因子产生)以及血浆神经丝定量。
24/25名参与者主观报告在给药末期疲劳增加;未检测到处理速度或自我报告的疲劳有变化。在给药末期,与中间访视相比,观察到产生干扰素γ的淋巴细胞(CD4 +:-57.7%,p = 0.01;CD8 +:-41.45%,p = 0.014;NK:-54.23%,p = 0.033)和其他促炎淋巴细胞亚群有选择性下降。此外,我们观察到GABA能皮质兴奋性的变化,在给药末期GABA - A依赖性对初级运动皮质的抑制增加(SICI,+46.9%,p = 0.026),GABA - B依赖性抑制(CSP)有类似趋势。血浆神经丝波动低于研究的检测能力。
在无临床或影像学疾病活动的情况下,促炎淋巴细胞在给药末期从外周循环中逸出。观察到的GABA依赖性皮质抑制变化可能反映了中枢神经系统淋巴细胞转运增加。未发现与给药末期症状有关联。