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Neuroinflammation in the peripheral nerve: cause, modulator, or bystander in peripheral neuropathies?

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-189696
  • The role of innate and adaptive inflammation as a primary driver or modifier of neuropathy in premorbidly normal nerves, and as a critical player in amplifying neuropathies of other known causes (e.g., genetic, metabolic) is incompletely understood and under-researched, despite unmet clinical need. Also, cellular and humoral components of the adaptive and innate immune system are substantial disease modifying agents in the context of neuropathies and, at least in some neuropathies, there is an identified tight interrelationship between bothThe role of innate and adaptive inflammation as a primary driver or modifier of neuropathy in premorbidly normal nerves, and as a critical player in amplifying neuropathies of other known causes (e.g., genetic, metabolic) is incompletely understood and under-researched, despite unmet clinical need. Also, cellular and humoral components of the adaptive and innate immune system are substantial disease modifying agents in the context of neuropathies and, at least in some neuropathies, there is an identified tight interrelationship between both compartments of the immune system. Additionally, the quadruple relationship between Schwann cell, axon, macrophage, and endoneurial fibroblast, with their diverse membrane bound and soluble signalling systems, forms a distinct focus for investigation in nerve diseases with inflammation secondary to Schwann cell mutations and possibly others. Identification of key immunological effector pathways that amplify neuropathic features and associated clinical symptomatology including pain should lead to realistic and timely possibilities for translatable therapeutic interventions using existing immunomodulators, alongside the development of novel therapeutic targets.zeige mehrzeige weniger

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Autor(en): Rudolf Martini, Hugh Willison
URN:urn:nbn:de:bvb:20-opus-189696
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Neurologische Klinik und Poliklinik
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):GLIA
Erscheinungsjahr:2016
Band / Jahrgang:64
Heft / Ausgabe:4
Seitenangabe:475-486
Originalveröffentlichung / Quelle:GLIA (2016) 64:4, S. 475-486. https://doi.org/10.1002/glia.22899
DOI:https://doi.org/10.1002/glia.22899
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):Charcot-Marie-Tooth; Guillain-Barré-Syndrom; Schwann cell dedifferentiation; adaptive immune system; familial amyloidotic polyneuropathy; fibroblast; glycation end products; innate immune system; lymphocytes; macrophage; motor axonal neuropathy; nodes of Ranvier
Datum der Freischaltung:14.01.2021
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International