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Therapeutic Plasma Exchange in Certain Immune-Mediated Neurological Disorders: Focus on a Novel Nanomembrane-Based Technology

Overview
Journal Biomedicines
Date 2023 Feb 25
PMID 36830870
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Abstract

Therapeutic plasma exchange (TPE) is an efficient extracorporeal blood purification technique to remove circulating autoantibodies and other pathogenic substances. Its mechanism of action in immune-mediated neurological disorders includes immediate intravascular reduction of autoantibody concentration, pulsed induction of antibody redistribution, and subsequent immunomodulatory changes. Conventional TPE with 1 to 1.5 total plasma volume (TPV) exchange is a well-established treatment in Guillain-Barre Syndrome, Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Neuromyelitis Optica Spectrum Disorder, Myasthenia Gravis and Multiple Sclerosis. There is insufficient evidence for the efficacy of so-called low volume plasma exchange (LVPE) (<1 TPV exchange) implemented either by the conventional or by a novel nanomembrane-based TPE in these neurological conditions, including their impact on conductivity and neuroregenerative recovery. In this narrative review, we focus on the role of nanomembrane-based technology as an alternative LVPE treatment option in these neurological conditions. Nanomembrane-based technology is a promising type of TPE, which seems to share the basic advantages of the conventional one, but probably with fewer adverse effects. It could play a valuable role in patient management by ameliorating neurological symptoms, improving disability, and reducing oxidative stress in a cost-effective way. Further research is needed to identify which patients benefit most from this novel TPE technology.

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References
1.
Maheshwari A, Sharma R, Prinja S, Hans R, Modi M, Sharma N . Cost-minimization analysis in the Indian subcontinent for treating Guillain Barre Syndrome patients with therapeutic plasma exchange as compared to intravenous immunoglobulin. J Clin Apher. 2018; 33(6):631-637. DOI: 10.1002/jca.21646. View

2.
Cortese I, Chaudhry V, So Y, Cantor F, Cornblath D, Rae-Grant A . Evidence-based guideline update: Plasmapheresis in neurologic disorders: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 2011; 76(3):294-300. PMC: 3034395. DOI: 10.1212/WNL.0b013e318207b1f6. View

3.
Kolev O, Kenarov P . Vestibular and ocular motor function prior to and after therapeutic apheresis with small plasmafilter in multiple sclerosis. J Clin Apher. 2015; 31(5):470-2. DOI: 10.1002/jca.21418. View

4.
van der Goes A, Brouwer J, Hoekstra K, Roos D, van den Berg T, Dijkstra C . Reactive oxygen species are required for the phagocytosis of myelin by macrophages. J Neuroimmunol. 1999; 92(1-2):67-75. DOI: 10.1016/s0165-5728(98)00175-1. View

5.
Lehmann H, Burke D, Kuwabara S . Chronic inflammatory demyelinating polyneuropathy: update on diagnosis, immunopathogenesis and treatment. J Neurol Neurosurg Psychiatry. 2019; 90(9):981-987. DOI: 10.1136/jnnp-2019-320314. View