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전신성홍반성낭창 환자에서 혈청내 sFas 및 sFas ligand 측정

Other Titles
 Determinations of Soluble Fas and Soluble Fas Ligand in Patients with Systemic Lupus Erythematosus 
Authors
 신정원  ;  김현숙  ;  송정식  ;  이수곤 
Citation
 Korean Journal of Clinical Pathology (대한임상병리학회지), Vol.19(2) : 234-238, 1999 
Journal Title
 Korean Journal of Clinical Pathology (대한임상병리학회지) 
ISSN
 1015-6445 
Issue Date
1999
Keywords
Apoptosis ; sFas ; sFas ligand ; Systemic lupus erythematosus (SLE)
Abstract
Background :The Fas/Fas ligand (FasL) system plays an important role in apoptosis by involvement in various immunologic functions, especially the removal of autoreactive and activated T-cells. sFas is a variant of the Fas receptor molecule, which lacks the transmembrane domain by alternative splicing of Fas mRNA and has an inhibitory effect in apoptosis by inhibition of the Fas/FasL pathway. sFasL is a coverted form of FasL by metalloproteinase and is increased in various malignant and autoimmune diseases. In this study, we investigated the expression of sFas and sFasL in systemic lupus erythematosus (SLE) and evaluated their usefulness as markers of disease activity. Method :The concentration of sFas and sFasL in sera from 43 patients with SLE, 17 with rheumatoid arthritis (RA) and 15 normal healthy persons were measured using sFas (S) ELISA Kit and sFas Ligand ELISA Kit (MBL Co., LTD., Nagoya, Japan), respectively. Twenty of 43 SLE sera were paired samples of 10 patients obtained on admission and discharge. Result :The concentration of sFas in SLE (3.12±2.28 ng/mL) was significantly higher than in RA (2.23±0.37 ng/mL) and in the normal control (2.12±0.33 ng/mL). In particular, the concentration of sFas in sera on admission (4.35±3.68 ng/mL) was significantly higher than in the sera on discharge (2.89±0.66 ng/mL), but, the concentration of sFasL among the 3 groups was not statistically different. Conclusion :These results suggest that apoptosis is involved in the pathogenesis of SLE and sFas might be a useful marker as a predictor of disease activity. Further study on the correlation between sFas and other disease activity markers, such as CRP, CH50, CD4 cell count and autoantibody titer is needed. Also, the evalution of sFas as a predictor of disease progression on follow-up studies of these patients is needed.
Files in This Item:
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Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
Yonsei Authors
Kim, Hyon Suk(김현숙) ORCID logo https://orcid.org/0000-0001-5662-7740
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/174171
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