Morse Brinkley A, Motovilov Katherine, Michael Brode W, Michael Tee Francis, Melamed Esther
Department of Neurology, Dell Medical School at the University of Texas, Austin, USA.
Department of Internal Medicine, Dell Medical School at the University of Texas, Austin, USA.
Brain Behav Immun. 2025 Jan;123:725-738. doi: 10.1016/j.bbi.2024.10.006. Epub 2024 Oct 9.
Intravenous immunoglobulin (IVIG) is an immunomodulatory therapy that has been studied in several neuroimmune conditions, such as Guillain-Barré Syndrome, chronic inflammatory demyelinating polyneuropathy, multifocal motor neuropathy, and multiple sclerosis. It has also been proposed as a potential treatment option for acute COVID-19 infection and post-acute sequelae of SARS-CoV-2 infection (PASC). IVIG is thought to function by providing the recipient with a pool of antibodies, which can, in turn, modulate immune responses through multiple mechanisms including neutralization of cytokines and autoantibodies, saturation of neonatal fragment crystallizable receptors, inhibition of complement activation, and regulation of T and B cell mediated inflammation. In acute COVID-19, studies have shown that early administration of IVIG and plasmapheresis in severe cases can reduce the need for mechanical ventilation, shorten ICU and hospital stays, and lower mortality. Similarly, in PASC, while research is still in early stages, IVIG has been shown to alleviate persistent symptoms in small patient cohorts. Furthermore, IVIG has shown benefits in another condition which has symptomatic overlap with PASC, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), though studies have yielded mixed results. It is important to note that IVIG can be associated with several potential adverse effects, such as anaphylaxis, headaches, thrombosis, liver enzyme elevations and renal complications. In addition, the high cost of IVIG can be a deterrent for payers and patients. This review provides a comprehensive update on the use of IVIG in multiple neuroimmune conditions, ME/CFS, acute COVID-19, and PASC, as well as covers its history, production, pricing, and mechanisms of action. We also identify key areas of future research, including the need to optimize the use of Ig product dosing, timing, and patient selection across conditions, particularly in the context of COVID-19 and PASC.
静脉注射免疫球蛋白(IVIG)是一种免疫调节疗法,已在多种神经免疫疾病中进行了研究,如格林-巴利综合征、慢性炎症性脱髓鞘性多发性神经病、多灶性运动神经病和多发性硬化症。它也被提议作为急性COVID-19感染和SARS-CoV-2感染后急性后遗症(PASC)的一种潜在治疗选择。IVIG被认为是通过为接受者提供一组抗体来发挥作用的,这些抗体进而可以通过多种机制调节免疫反应,包括中和细胞因子和自身抗体、饱和新生儿片段可结晶受体、抑制补体激活以及调节T和B细胞介导的炎症。在急性COVID-19中,研究表明,在重症病例中早期给予IVIG和血浆置换可以减少机械通气的需求,缩短重症监护病房(ICU)和住院时间,并降低死亡率。同样,在PASC中,虽然研究仍处于早期阶段,但已表明IVIG可减轻小患者队列中的持续症状。此外,IVIG在另一种与PASC有症状重叠的疾病——肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)中也显示出益处,不过研究结果不一。需要注意的是,IVIG可能与多种潜在不良反应相关,如过敏反应、头痛、血栓形成、肝酶升高和肾脏并发症。此外,IVIG的高成本可能会对支付方和患者起到阻碍作用。本综述全面更新了IVIG在多种神经免疫疾病、ME/CFS、急性COVID-19和PASC中的应用情况,还涵盖了其历史、生产、定价和作用机制。我们还确定了未来研究的关键领域,包括需要优化Ig产品剂量、给药时间和不同疾病的患者选择,特别是在COVID-19和PASC的背景下。