Anti-inflammatory actions of intravenous immunoglobulin

被引:418
作者
Nimmerjahn, Falk [1 ]
Ravetch, Jeffrey V. [2 ]
机构
[1] Univ Erlangen Nurnberg, Nikolaus Fiebiger Ctr Mol Med, Lab Expt Immunol & Immunotherapy, D-91054 Erlangen, Germany
[2] Rockefeller Univ, Lab Mol Genet & Immunol, New York, NY 10021 USA
关键词
Fc receptor; inflammation; glycosylation; autoimmunity; autoantibody; sialic acid; IVIG;
D O I
10.1146/annurev.immunol.26.021607.090232
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The remarkable success story of the therapeutic application of pooled immunoglobulin G (IgG) preparations from thousands of donors, the so-called intravenous IgG (IVIG) therapy, to patients with a variety of hematological and immunological disorders began more than half a century ago. Since then, the use of this primary blood product has increased constantly, resulting in the serious danger of shortages in supply. Despite its widespread use and therapeutic success, the mechanisms of action, especially of the anti-inflammatory activity, are only beginning to be understood. In this review, we summarize the clinical use of IVIG for different diseases and discuss recent data on the molecular mechanisms that might explain how this potent drug mediates its activity in vivo.
引用
收藏
页码:513 / 533
页数:21
相关论文
共 107 条
[51]   Fates of human B-cell precursors [J].
LeBien, TW .
BLOOD, 2000, 96 (01) :9-23
[52]   Complete FcRn dependence for intravenous Ig therapy in autoimmune skin blistering diseases [J].
Li, N ;
Zhao, ML ;
Hilario-Vargas, J ;
Prisayanh, P ;
Warren, S ;
Diaz, LA ;
Roopenian, DC ;
Liu, Z .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (12) :3440-3450
[53]   Amelioration of experimental autoimmune myasthenia gravis in rats by neonatal FcR blockade [J].
Liu, Liming ;
Garcia, Ana Maria ;
Santoro, Helen ;
Zhang, Yixia ;
McDonnell, Kevin ;
Dumont, Jennifer ;
Bitonti, Alan .
JOURNAL OF IMMUNOLOGY, 2007, 178 (08) :5390-5398
[54]   GLYCOSYLATION CHANGES OF IGG ASSOCIATED WITH RHEUMATOID-ARTHRITIS CAN ACTIVATE COMPLEMENT VIA THE MANNOSE-BINDING PROTEIN [J].
MALHOTRA, R ;
WORMALD, MR ;
RUDD, PM ;
FISCHER, PB ;
DWEK, RA ;
SIM, RB .
NATURE MEDICINE, 1995, 1 (03) :237-243
[55]   HUMAN AUTOANTIBODIES REACTIVE WITH SYNTHETIC AUTOANTIGENS FROM T-CELL RECEPTOR BETA-CHAIN [J].
MARCHALONIS, JJ ;
KAYMAZ, H ;
DEDEOGLU, F ;
SCHLUTER, SF ;
YOCUM, DE ;
EDMUNDSON, AB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (08) :3325-3329
[56]   ELIMINATION OF INFECTIOUS ANTIGENS AND INCREASE OF IGG CATABOLISM AS POSSIBLE MODES OF ACTION OF IVIG [J].
MASSON, PL .
JOURNAL OF AUTOIMMUNITY, 1993, 6 (06) :683-689
[57]   Autoantibody activity of IgG rheumatoid factor increases with decreasing levels of galactosylation and sialylation [J].
Matsumoto, A ;
Shikata, K ;
Takeuchi, F ;
Kojima, N ;
Mizuochi, T .
JOURNAL OF BIOCHEMISTRY, 2000, 128 (04) :621-628
[58]  
Mimura Y, 2001, ADV EXP MED BIOL, V495, P49
[59]  
MIZUOCHI T, 1990, J IMMUNOL, V145, P1794
[60]  
Molica S, 1996, HAEMATOLOGICA, V81, P121