Elevated serum levels of soluble membrane cofactor protein (CD46, MCP) in patients with systemic lupus erythematosus (SLE)

被引:0
作者
Kawano, M
Seya, T
Koni, I
Mabuchi, H
机构
[1] Kanazawa Univ, Sch Med, Dept Internal Med 2, Kanazawa, Ishikawa 9208641, Japan
[2] Osaka Med Ctr Canc & Cardiovasc Dis, Dept Immunol, Osaka, Japan
关键词
membrane cofactor protein (CD46); soluble CD46; systemic lupus erythematosus;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Membrane cofactor protein (MCP, CD46) is a cell surface complement regulatory protein which acts as a cofactor for the factor I-mediated cleavage of the activated complement components C3b/C4b. To evaluate the clinical usefulness of serum soluble CD46 as a marker of disease activity in patients with SLE, serum levels of sCD46 were measured by ELISA, using two MoAbs (M160 and M177), each of which recognized two different epitopes on CD46 molecule in SLE, other autoimmune diseases and healthy controls. Serum sCD46 levels in active SLE patients (30.5 +/- 14.1 ng/ml) were significantly higher than those of inactive SLE (5.8 +/- 7.1 ng/ml; P = 0.0003), rheumatoid arthritis (14.9 +/- 11.6 ng/ ml; P = 0.0218), primary Sjogren's syndrome (12.3 +/- 11.6 ng/ml; P = 0.0039) and normal controls (7.3 +/- 3.6 ng/ml; P = 0.0005). The elevated serum sCD46 levels in active SLE patients significantly decreased from 30.5 +/- 14.1 ng/ml to 8.0 +/- 6.3 ng/ml after effective corticosteroid and immunosuppressant therapy (P = 0.018). Additionally, we found a significant negative association between increasing concentration of sCD46 and decreasing levels of CH50 in SLE (r = 0.598, P = 0.0009). These results suggest that sCD46 reflects in vivo activation of complement system and provides an additional useful serum parameter of active SLE.
引用
收藏
页码:542 / 546
页数:5
相关论文
共 24 条
  • [1] ARNETT FC, 1987, ARTHRITIS RHEUM, V31, P315
  • [2] DERIVATION OF THE SLEDAI - A DISEASE-ACTIVITY INDEX FOR LUPUS PATIENTS
    BOMBARDIER, C
    GLADMAN, DD
    UROWITZ, MB
    CARON, D
    CHANG, CH
    [J]. ARTHRITIS AND RHEUMATISM, 1992, 35 (06): : 630 - 640
  • [3] A functional analysis of recombinant soluble CD46 in vivo and a comparison with recombinant soluble forms of CD55 and CD35 in vitro
    Christiansen, D
    Milland, J
    Thorley, BR
    McKenzie, IFC
    Loveland, BE
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (03) : 578 - 585
  • [4] IDENTIFICATION OF AN ADDITIONAL CLASS OF C3-BINDING MEMBRANE-PROTEINS OF HUMAN PERIPHERAL-BLOOD LEUKOCYTES AND CELL-LINES
    COLE, JL
    HOUSLEY, GA
    DYKMAN, TR
    MACDERMOTT, RP
    ATKINSON, JP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (03) : 859 - 863
  • [5] CD59, AN LY-6-LIKE PROTEIN EXPRESSED IN HUMAN LYMPHOID-CELLS, REGULATES THE ACTION OF THE COMPLEMENT MEMBRANE ATTACK COMPLEX ON HOMOLOGOUS CELLS
    DAVIES, A
    SIMMONS, DL
    HALE, G
    HARRISON, RA
    TIGHE, H
    LACHMANN, PJ
    WALDMANN, H
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (03) : 637 - 654
  • [6] ENDOH M, 1993, CLIN EXP IMMUNOL, V94, P182
  • [7] FALK RJ, 1985, NEW ENGL J MED, V315, P1584
  • [8] GARWRYL MA, 1988, ARTHRITIS RHEUM, V31, P188
  • [9] GAUTHIER VJ, 1997, DUBOIS LUPUS ERYTHEM, P207
  • [10] HARA T, 1992, CLIN EXP IMMUNOL, V89, P490