کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2830704 1163750 2015 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Ficolins and the lectin pathway of complement in patients with systemic lupus erythematosus
ترجمه فارسی عنوان
فیکولین و مسیر لکتین مکمل در بیماران مبتلا به لوپوس اریتماتوز سیستمیک؟
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شناسی مولکولی
چکیده انگلیسی


• Ficolin1 plasma concentration is correlated wih disease activity in SLE patients.
• Ficolin-1 plasma concentration is correlated with damage score and arterial thrombosis.
• Function of the ficolin-3 pathway is associated with disease activity.
• The ficolins may be involved in the pathohysiology of SLE.

The complement system plays a pathophysiological role in systemic lupus erythematosus (SLE). This study aims to investigate whether an association exists between the ficolins that are part of the lectin complement pathway and SLE.EDTA plasma samples from 68 Danish SLE patients and 29 healthy donors were included in the study. Plasma concentrations of Ficolin-1, -2, and -3 were determined in specific sandwich ELISAs. Lectin pathway activity via Ficolin-3 was measured in ELISA on acetylated bovine serum albumin (acBSA) and measured as Ficolin-3 binding and deposition of C4, C3 and the terminal complement complex (TCC).SLE patients had increased levels of Ficolin-3, 21.6 μg/ml as compared to 17.0 μg/ml in healthy controls (P = 0.0098). The Ficolin-1 plasma concentration was negatively correlated with SLE Disease Activity Index (SLEDAI) (Rho = −0.29, P = 0.015) and positively correlated to the [Systemic Lupus International Collaborating Clinics (SLICC)/American College of Rheumatology (ACR) Damage Index] (SDI) (Rho = 0.27, P = 0.026). The Ficolin-1 concentration was also associated with the occurrence of arterial (P = 0.0053) but not venous thrombosis (P = 0.42). Finally, deposition of C4, C3 and TCC in the Ficolin-3 pathway were all correlated to SLEDAI, respectively (P < 0.0076).The Ficolin-1 association to SLEDAI and SDI as well as arterial thrombosis shown in this study suggests that Ficolin-1 may be a potential new biomarker for patients with SLE. Furthermore, Ficolin-3 mediated complement activation may be valuable in monitoring disease activity in SLE patients due to the high sensitivity for complement consumption in the assay independent of the Ficolin-3 concentration.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Molecular Immunology - Volume 63, Issue 2, February 2015, Pages 209–214
نویسندگان
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