Elevated levels of the soluble form of bone marrow stromal cell antigen 1 in the sera of patients with severe rheumatoid arthritis

被引:33
作者
Lee, BO
Ishihara, K
Denno, K
Kobune, Y
Itoh, M
Muraoka, O
Kaisho, T
Sasaki, T
Ochi, T
Hirano, T
机构
[1] OSAKA UNIV,SCH MED,BIOMED RES CTR,DIV MOLEC ONCOL,SUITA,OSAKA 565,JAPAN
[2] TOHOKU UNIV,SCH MED,SENDAI,MIYAGI 980,JAPAN
来源
ARTHRITIS AND RHEUMATISM | 1996年 / 39卷 / 04期
关键词
D O I
10.1002/art.1780390414
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Bone marrow stromal cell antigen 1 (BST-1) is a novel glycosyl phosphatidylinositol-anchored ectoenzyme, which is overexpressed on bone marrow stromal and synovial cell lines derived from patients with rheumatoid arthritis (RA). To investigate the pathophysiologic roles of BST-1 in RA, we established an enzyme-linked immunosorbent assay (ELISA) system to detect the soluble form of BST-1 (sBST-1) and examined levels of sBST-1 in the sera of RA patients. Methods. Concentrations of sBST-1 in sera from healthy donors and from patients with RA, osteoarthritis, Sjogren's syndrome, and systemic lupus erythematosus were measured with the ELISA. Results. In 7% of the RA patient samples (10 of 143), concentrations of serum sBST-1 were higher (similar to 30-50-fold) than in non-RA samples. Serum sBST-1 concentrations showed no correlation with age, C-reactive protein level, or rheumatoid factor level. All RA patients with high concentrations of serum sBST-1 had severe disease with involvement of several large joints. Conclusion. We believe the measurement of serum sBST-1 may have prognostic value, but further analysis is necessary to clarify the clinical significance of elevated sBST-1 in RA.
引用
收藏
页码:629 / 637
页数:9
相关论文
共 33 条
[21]  
Kincade P W, 1991, Semin Immunol, V3, P379
[22]   CYCLIC ADP-RIBOSE - METABOLISM AND CALCIUM MOBILIZING FUNCTION [J].
LEE, HC ;
GALIONE, A ;
WALSETH, TF .
VITAMINS AND HORMONES - ADVANCES IN RESEARCH AND APPLICATIONS, VOL 48, 1994, 48 :199-257
[23]  
LIPSKY PE, 1991, HARRISONS PRINCIPLES
[24]  
MARTIN S, 1995, J IMMUNOL, V154, P1951
[25]   INTERLEUKIN-6-INDUCED TYROSINE PHOSPHORYLATION OF MULTIPLE PROTEINS IN MURINE HEMATOPOIETIC LINEAGE CELLS [J].
MATSUDA, T ;
YAMANAKA, Y ;
HIRANO, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 200 (02) :821-828
[26]  
MCNIECE IK, 1991, J IMMUNOL, V146, P3785
[27]   RELEASE OF GPI-ANCHORED MEMBRANE-PROTEINS BY A CELL-ASSOCIATED GPI-SPECIFIC PHOSPHOLIPASE-D [J].
METZ, CN ;
BRUNNER, G ;
CHOIMUIRA, NH ;
NGUYEN, H ;
GABRILOVE, J ;
CARAS, IW ;
ALTSZULER, N ;
RIFKIN, DB ;
WILSON, EL ;
DAVITZ, MA .
EMBO JOURNAL, 1994, 13 (07) :1741-1751
[28]   STIMULATION OF B-CELL PROGENITORS BY CLONED MURINE INTERLEUKIN-7 [J].
NAMEN, AE ;
LUPTON, S ;
HJERRILD, K ;
WIGNALL, J ;
MOCHIZUKI, DY ;
SCHMIERER, A ;
MOSLEY, B ;
MARCH, CJ ;
URDAL, D ;
GILLIS, S ;
COSMAN, D ;
GOODWIN, RG .
NATURE, 1988, 333 (6173) :571-573
[29]   NATURAL COURSE OF JOINT DESTRUCTION AND FLUCTUATION OF SERUM C1Q LEVELS IN PATIENTS WITH RHEUMATOID-ARTHRITIS [J].
OCHI, T ;
IWASE, R ;
YONEMASU, K ;
MATSUKAWA, M ;
YONEDA, M ;
YUKIOKA, M ;
ONO, K .
ARTHRITIS AND RHEUMATISM, 1988, 31 (01) :37-43
[30]  
PINOOTIN MR, 1995, J IMMUNOL, V154, P3015