Literature DB >> 23791035

Polyclonal immunoglobulin G for autoimmune demyelinating nervous system disorders.

Mathias Buttmann1, Srini Kaveri, Hans-Peter Hartung.   

Abstract

Demyelinating diseases with presumed autoimmune pathogenesis are characterised by direct or indirect immune-mediated damage to myelin sheaths, which normally surround nerve fibres to ensure proper electrical nerve conduction. Parenteral administration of polyclonal IgG purified from multi-donor human plasma pools may beneficially modulate these misguided immune reactions via several mechanisms that are outlined in this review. Convincing therapeutic evidence from controlled trials now exists for certain disorders of the peripheral nervous system, including Guillain-Barré syndrome, chronic inflammatory demyelinating polyradiculoneuropathy, and multifocal motor neuropathy. In addition, there is evidence for potential therapeutic benefits of IgG in patients with chronic inflammatory demyelinating diseases of the central nervous system, including multiple sclerosis and neuromyelitis optica. This review introduces these disorders, briefly summarises the established treatment options, and discusses therapeutic evidence for the use of polyclonal immunoglobulins with a particular emphasis on recent clinical trials and meta-analyses.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Guillain–Barré syndrome; clinical trials; immunoglobulins; multiple sclerosis; neuromyelitis optica; polyradiculoneuropathy

Mesh:

Substances:

Year:  2013        PMID: 23791035     DOI: 10.1016/j.tips.2013.05.009

Source DB:  PubMed          Journal:  Trends Pharmacol Sci        ISSN: 0165-6147            Impact factor:   14.819


  7 in total

1.  Immunoglobulins stimulate cultured Schwann cell maturation and promote their potential to induce axonal outgrowth.

Authors:  Nevena Tzekova; André Heinen; Sebastian Bunk; Corinna Hermann; Hans-Peter Hartung; Birgit Reipert; Patrick Küry
Journal:  J Neuroinflammation       Date:  2015-05-29       Impact factor: 8.322

2.  Endogenous antibodies contribute to macrophage-mediated demyelination in a mouse model for CMT1B.

Authors:  Dennis Klein; Janos Groh; Andreas Weishaupt; Rudolf Martini
Journal:  J Neuroinflammation       Date:  2015-03-12       Impact factor: 8.322

3.  Dose-dependent inhibition of demyelination and microglia activation by IVIG.

Authors:  Meike Winter; Christine Baksmeier; Julia Steckel; Sumanta Barman; Manish Malviya; Melanie Harrer-Kuster; Hans-Peter Hartung; Norbert Goebels
Journal:  Ann Clin Transl Neurol       Date:  2016-09-23       Impact factor: 4.511

4.  Regulatory T cell frequency, but not plasma IL-33 levels, represents potential immunological biomarker to predict clinical response to intravenous immunoglobulin therapy.

Authors:  Mohan S Maddur; Emmanuel Stephen-Victor; Mrinmoy Das; Praveen Prakhar; Varun K Sharma; Vikas Singh; Magalie Rabin; Jamma Trinath; Kithiganahalli N Balaji; Francis Bolgert; Jean-Michel Vallat; Laurent Magy; Srini V Kaveri; Jagadeesh Bayry
Journal:  J Neuroinflammation       Date:  2017-03-20       Impact factor: 8.322

5.  Risk Factors of Neurological Complications in Severe Fever Patients with Thrombolytic Syndrome: A Single-Center Retrospective Study in China.

Authors:  Xiao Fei; Kai Fang; Xiuying Ni; Wan-Hua Ren
Journal:  Med Sci Monit       Date:  2021-11-08

6.  Chronic inflammatory demyelinating polyneuropathy (CIDP): change of serum IgG dimer levels during treatment with intravenous immunoglobulins.

Authors:  Christian Ritter; Ilja Bobylev; Helmar C Lehmann
Journal:  J Neuroinflammation       Date:  2015-08-14       Impact factor: 8.322

7.  Heme oxygenase-1 is dispensable for the anti-inflammatory activity of intravenous immunoglobulin.

Authors:  Caroline Galeotti; Pushpa Hegde; Mrinmoy Das; Emmanuel Stephen-Victor; Fernando Canale; Marcos Muñoz; Varun K Sharma; Jordan D Dimitrov; Srini V Kaveri; Jagadeesh Bayry
Journal:  Sci Rep       Date:  2016-01-22       Impact factor: 4.379

  7 in total

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