New perspectives in treatment of glomerulonephritis

被引:25
作者
Coppo, R
Amore, A
机构
[1] Osped Infantile Regina Margherita, Nephrol Dialysis & Transplantat Dept, I-10126 Turin, Italy
[2] Regina Margherita Childrens Univ Hosp, Nephrol Dialysis & Transplantat Dept, Turin, Italy
关键词
glomerulonephritis; treatment; antigen eradication; mycophenolate mofetil; rapamycin; anti-adhesion molecules; anti-co-stimulatory molecules; anti-inflammatory cytokines; anti-CD20; anti-COX2; thalidomide pirfenidone; PPAR;
D O I
10.1007/s00467-003-1357-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
In chronic glomerulonephritis (GN) the development of the tissue damage and progression to fibrosis is related to the individual immune response which brings about excessive inflammation, failure to activate regression and glomerular repair and excessive fibrogenic activity. Therefore, the present standard treatment of GN has two aims, to fight the acute inflammation and to inhibit the progressive renal fibrosis. New avenues in the anti-inflammatory and immunosuppressive treatment of the active phase of glomerular diseases include the use of drugs proven to be of value in organ transplantation (mycophenolate mofetil, rapamycin or anti-immune adhesion and anti-co-stimulatory molecules). Interest has recently focused on anti-inflammatory cytokines (monoclonal antibodies, peptidic antagonists or anti-sense oligonucleotides against TNF-alpha, anti-PDGF-beta, anti-TGF-beta and cytokine receptor antagonists) and anti-inflammatory natural cytokines (such as IL4, IL10, IL13 or low doses of TGFbeta). Other drugs may act by depleting B cells (such as anti-CD20 monoclonal antibody) or on several immune pathways, such as thalidomide or anti-cyclooxygenase 2. Several anti-sclerogenic drugs are already used for treatment of the chronic phase of glomerular diseases, such as antagonists of angiotensin II, statins and antioxidants. Other drugs are still experimental, including endothelin receptor antagonists and neutral endopeptidase or vasopeptidase inhibitors and other drugs operating on extracellular matrix accumulation/degradation mechanisms, e.g., pirfenidone. There are extremely interesting developments concerning activators of endogenous anti-inflammatory mechanisms, such as those regulated by peroxisome proliferator activated receptors. There is a need for successful treatment of chronic GN in childhood. This short review of the most promising new drugs shows there is reason to believe that the next decade will provide exciting new tools for the treatment of these diseases in children.
引用
收藏
页码:256 / 265
页数:10
相关论文
共 60 条
[1]  
Abbate M, 1998, J AM SOC NEPHROL, V9, P1213
[2]  
Aeberli D, 2002, SWISS MED WKLY, V132, P414
[3]  
Amore A, 2001, J AM SOC NEPHROL, V12, P1862, DOI 10.1681/ASN.V1291862
[4]   The relationship of FcγRIIIa genotype to degree of B cell depletion by rituximab in the treatment of systemic lupus erythematosus [J].
Anolik, JH ;
Campbell, D ;
Felgar, RE ;
Young, F ;
Sanz, I ;
Rosenblatt, J ;
Looney, RJ .
ARTHRITIS AND RHEUMATISM, 2003, 48 (02) :455-459
[5]  
ARDAILLOU R, 2000, KIDNEY, V1, P93
[6]   Treatment of refractory antibody mediated autoimmune disorders with an anti-CD20 monoclonal antibody (rituximab) [J].
Arzoo, K ;
Sadeghi, S ;
Liebman, HA .
ANNALS OF THE RHEUMATIC DISEASES, 2002, 61 (10) :922-924
[7]   Cytokines and hormones with anti inflammatory effects: new tools for therapeutic intervention [J].
Baud, L ;
Fouqueray, B ;
Bellocq, A .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2001, 10 (01) :49-54
[8]   Endothelin antagonists [J].
Benigni, A ;
Remuzzi, G .
LANCET, 1999, 353 (9147) :133-138
[9]   Anti-intercellular Adhesion molecule-1 (ICAM-1) antibody treatment prevents central and peripheral nervous system disease in autoimmune-prone mice [J].
Brey, RL ;
Amato, AA ;
KaganHallet, K ;
Rhine, CB ;
Stallworth, CL .
LUPUS, 1997, 6 (08) :645-651
[10]   Successful mycophenolate mofetil treatment of glomerular disease [J].
Briggs, WA ;
Choi, MJ ;
Scheel, PJ .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 31 (02) :213-217