BAFF is elevated in serum of patients with Wegener's granulomatosis

被引:115
作者
Krumbholz, M
Specks, U
Wick, M
Kalled, SL
Jenne, D
Meinl, E
机构
[1] Max Planck Inst Neurobiol, Dept Neuroimmunol, D-82152 Martinsried, Germany
[2] Univ Munich, Inst Clin Neuroimmunol, Munich, Germany
[3] Mayo Clin, Div Pulm & Crit Care Med, Rochester, MN USA
[4] Univ Munich, Inst Clin Chem, Munich, Germany
[5] Biogen Idec, Cambridge, MA USA
关键词
autoantibody; B-cell activating factor of TNF family (BAFF); human; serum; Wegener's granulomatosis;
D O I
10.1016/j.jaut.2005.08.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BAFF (B-cell activating factor of the TNF family) plays a crucial role in B-cell Survival. Elevated BAFF serum levels have been linked to several autoimmune diseases in humans, and therapies targeting BAFF were successful in animal models of rheumatoid arthritis and systemic lupus erythematosus. Wagener's granulomatosis (WG), a chronic systemic vasculitis, is characterized by circulating autoantibodies (cANCA) targeting neutrophils, which can produce BAFF To investigate whether BAFF is involved in WG pathology, BAFF serum levels were measured by ELISA in 46 WG patients and 62 healthy donors. We report the novel finding that in WG patients serum levels of BAFF were significantly increased (median 3.95 ng/ml, p = 0.009) compared to healthy controls (median 2.38 ng/ml). The difference was even more pronounced when comparing controls with untreated WG patients (median 4.61 ng/ml, p = 0.001). Treatment of WG patients with glucocorticoids was associated with lower BAFF levels. The serum BAFF level in treated WG patients was about the same as in the control group. We propose that BAFF might be a pathogenic factor in WG and that targeting BAFF may represent a new therapeutic strategy in a subset of chronically relapsing WG patients with elevated BAFF levels. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:298 / 302
页数:5
相关论文
共 21 条
[1]   BLyS - an essential survival factor for B cells: basic biology, links to pathology and therapeutic target [J].
Baker, KP .
AUTOIMMUNITY REVIEWS, 2004, 3 (05) :368-375
[2]  
Cheema GS, 2001, ARTHRITIS RHEUM-US, V44, P1313, DOI 10.1002/1529-0131(200106)44:6<1313::AID-ART223>3.0.CO
[3]  
2-S
[4]   Normal B cell homeostasis requires B cell activation factor production by radiation-resistant cells [J].
Gorelik, L ;
Gilbride, K ;
Dobles, M ;
Kalled, SL ;
Zandman, D ;
Scott, ML .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 198 (06) :937-945
[5]   Association of BAFF/BLyS overexpression and altered B cell differentiation with Sjogren's syndrome [J].
Groom, J ;
Kalled, SL ;
Cutler, AH ;
Olson, C ;
Woodcock, SA ;
Schneider, P ;
Tschopp, J ;
Cachero, TG ;
Batten, M ;
Wheway, J ;
Mauri, D ;
Cavill, D ;
Gordon, TP ;
Mackay, CR ;
Mackay, F .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (01) :59-68
[6]   Analysis on the association of human BLYS (BAFF TNFSF13B) polymorphisms with systemic lupus erythematosus and rheumatoid arthritis [J].
Kawasaki, A ;
Tsuchiya, N ;
Fukazawa, T ;
Hashimoto, H ;
Tokunaga, K .
GENES AND IMMUNITY, 2002, 3 (07) :424-429
[7]   Peripheral blood and granuloma CD4+CD28- T cells are a major source of interferon-γ and tumor necrosis factor-α in Wegener's granulomatosis [J].
Komocsi, A ;
Lamprecht, P ;
Csernok, E ;
Mueller, A ;
Holl-Ulrich, K ;
Seitzer, U ;
Moosig, F ;
Schnabel, A ;
Gross, WL .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (05) :1717-1724
[8]   BAFF is produced by astrocytes and up-regulated in multiple sclerosis lesions and primary central nervous system lymphoma [J].
Krumbholz, M ;
Theil, D ;
Derfuss, T ;
Rosenwald, A ;
Schrader, F ;
Monoranu, CM ;
Kalled, SL ;
Hess, DM ;
Serafini, B ;
Aloisi, F ;
Wekerle, H ;
Hohlfeld, R ;
Meinl, E .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (02) :195-200
[9]   BAFF and APRIL: A tutorial on B cell survival [J].
Mackay, F ;
Schneider, P ;
Rennert, P ;
Browning, J .
ANNUAL REVIEW OF IMMUNOLOGY, 2003, 21 :231-264
[10]   Levels of BAFF in serum in primary biliary cirrhosis and autoimmune diabetes [J].
Mackay, IR ;
Groom, J ;
Mackay, CR .
AUTOIMMUNITY, 2002, 35 (08) :551-553