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Verfasst von:Schlößer, Lukas [VerfasserIn]   i
 Klose, Sara M. [VerfasserIn]   i
 Mauschitz, Matthias [VerfasserIn]   i
 Abdullah, Zeinab [VerfasserIn]   i
 Finger, Robert P. [VerfasserIn]   i
Titel:The role of immune modulators in age-related macular degeneration
Verf.angabe:Lukas Schloesser, Sara M. Klose, Matthias M. Mauschitz, Zeinab Abdullah, Robert P. Finger
E-Jahr:2024
Jahr:November-December 2024
Umfang:19 S.
Illustrationen:Illustrationen
Fussnoten:Online verfügbar: 6. August 2024, Artikelversion: 10 September 2024 ; Gesehen am 25.11.2025
Titel Quelle:Enthalten in: Survey of ophthalmology
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1975
Jahr Quelle:2024
Band/Heft Quelle:69(2024), 6, Seite 851-869
ISSN Quelle:1879-3304
Abstract:We provide an overview of the expanding literature on the role of cytokines and immune mediators in pathophysiology of age-related macular degeneration (AMD). Although many immunological mediators have been linked to AMD pathophysiology, the broader mechanistic picture remains unclear with substantial variations in the levels of evidence supporting these mediators. Therefore, we reviewed the literature considering the varying levels of supporting evidence. A Medical Subject Headings (MeSH) term-based literature research was conducted in September, 2023, consisting of the MeSH terms “cytokine” and “Age-related macular degeneration” connected by the operator “AND”. After screening the publications by title, abstract, and full text, a total of 146 publications were included. The proinflammatory cytokines IL-1β (especially in basic research studies), IL-6, IL-8, IL-18, TNF-α, and MCP-1 are the most extensively characterised cytokines/chemokines, highlighting the role of local inflammasome activation and altered macrophage function in the AMD pathophysiology. Among the antiinflammatory mediators IL-4, IL-10, and TGF-β were found to be the most extensively characterised, with IL-4 driving and IL-10 and TGF-β suppressing disease progression. Despite the extensive literature on this topic, a profound understanding of AMD pathophysiology has not yet been achieved. Therefore, further studies are needed to identify potential therapeutic targets, followed by clinical studies
DOI:doi:10.1016/j.survophthal.2024.07.009
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.survophthal.2024.07.009
 Volltext: https://www.sciencedirect.com/science/article/pii/S0039625724000845
 DOI: https://doi.org/10.1016/j.survophthal.2024.07.009
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Age related macular degeneration
 AMD
 Complement
 Cytokines
 Inflammasome
 Innate immunity
 Macrophages
K10plus-PPN:1909438499
Verknüpfungen:→ Zeitschrift

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