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Zipplies, J.K.* ; Kirschfink, M.* ; Amann, B.* ; Hauck, S.M. ; Stangassinger, M.* ; Deeg, C.A.*

Complement factor B expression profile in a spontaneous uveitis model.

Immunobiology 215, 949-955 (2010)
DOI PMC
Open Access Gold as soon as Publ. Version/Full Text is submitted to ZB.
Equine recurrent uveitis serves as a spontaneous model for human autoimmune uveitis. Unpredictable relapses and ongoing inflammation in the eyes of diseased horses as well as in humans lead to destruction of the retina and finally result in blindness. However, the molecular mechanisms leading to inflammation and retinal degeneration are not well understood. An initial screening for differentially regulated proteins in sera of uveitic cases compared to healthy controls revealed an increase of the alternative pathway complement component factor B in ERU cases. To determine the activation status of the complement system, sera were subsequently examined for complement split products. We could demonstrate a significant higher concentration of the activation products B/Ba, B/Bb, Bb neoantigen, iC3b and C3d in uveitic condition compared to healthy controls, whereas for C5b-9 no differences were detected. Additionally, we investigated complement activation directly in the retina by immunohistochemistry, since it is the main target organ of this autoimmune disease. Interestingly, infiltrating cells co-expressed activated factor Bb neoantigen, complement split product C3d as well as CD68, a macrophage marker. In this study, we could demonstrate activation of the complement system both systemically as well as in the eye, the target organ of spontaneous recurrent uveitis. Based on these novel findings, we postulate a novel role for macrophages in connection with complement synthesis at the site of inflammation.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Autoimmune; Complement system; Serum; Uveitis; Vitreous
Language english
Publication Year 2010
HGF-reported in Year 2010
ISSN (print) / ISBN 0171-2985
e-ISSN 1878-3279
Quellenangaben Volume: 215, Issue: 12, Pages: 949-955 Article Number: , Supplement: ,
Publisher Urban & Fischer
Reviewing status Peer reviewed
POF-Topic(s) 30203 - Molecular Targets and Therapies
Research field(s) Enabling and Novel Technologies
PSP Element(s) G-505700-001
PubMed ID 20334949
Scopus ID 78049238579
Erfassungsdatum 2010-12-01