The role of complement in biomaterial-induced inflammation

被引:302
作者
Nilsson, Bo
Ekdahl, Kristina Nilsson [1 ]
Mollnes, Tom Eirik
Lambris, John D.
机构
[1] Univ Uppsala Hosp, Dept Radiol Oncol & Clin Immunol, Div Clin Immunol, Rudbeck Lab, Uppsala, Sweden
[2] Univ Kalmar, Dept Chem & Biomed Sci, Kalmar, Sweden
[3] Rikshosp Univ Hosp, Inst Immunol, Oslo, Norway
[4] Univ Oslo, N-0316 Oslo, Norway
[5] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词
complement; biomaterial; coagulation; inflammation; cross-talk;
D O I
10.1016/j.molimm.2006.06.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Biomaterials are regularly used in various types of artificial tissues and organs, such as oxygenators, plasmapheresis equipment, hemodialysers, catheters, prostheses, stents, vascular grafts, miniature pumps, sensors and heart aids. Although progress has been made regarding bioincompatibility, many materials and procedures are associated with side effects, in particular bioincompatibility-induced inflammation, infections and subsequent loss of function. After cardiopulmonary bypass, coagulopathies can occur and lead to cognitive disturbances, stroke and extended hospitalization. Hemodialysis is associated with anaphylatoid reactions that cause whole-body inflammation and may contribute to accelerated arteriosclerosis. Stents cause restenosis and, in severe cases, thrombotic reactions. This situation indicates that there is still a need to try to understand the mechanisms involved in these incompatibility reactions in order to be able to improve the biomaterials and to develop treatments that attenuate the reactions and thereby reduce patients' discomfort, treatment time and cost. This overview deals with the role of complement in the incompatibility reactions that occur when biomaterials come in contact with blood and other body fluids. (C) 2006 Published by Elsevier Ltd.
引用
收藏
页码:82 / 94
页数:13
相关论文
共 109 条
[31]   Biomaterial-associated thrombosis: roles of coagulation factors, complement, platelets and leukocytes [J].
Gorbet, MB ;
Sefton, MV .
BIOMATERIALS, 2004, 25 (26) :5681-5703
[32]   Whole blood coagulation on protein adsorption-resistant PEG and peptide functionalised PEG-coated titanium surfaces [J].
Hansson, KM ;
Tosatti, S ;
Isaksson, J ;
Wetterö, J ;
Textor, M ;
Lindahl, TL ;
Tengvall, P .
BIOMATERIALS, 2005, 26 (08) :861-872
[33]   The quantitative role of alternative pathway amplification in classical pathway induced terminal complement activation [J].
Harboe, M ;
Ulvund, G ;
Vien, L ;
Fung, M ;
Mollnes, TE .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2004, 138 (03) :439-446
[34]   Inhibition of C5a-induced neutrophil chemotaxis and macrophage cytokine production in vitro by a new C5a receptor antagonist [J].
Haynes, DR ;
Harkin, DG ;
Bignold, LP ;
Hutchens, MJ ;
Taylor, SM ;
Fairlie, DP .
BIOCHEMICAL PHARMACOLOGY, 2000, 60 (05) :729-733
[35]   COMPLEMENT ACTIVATION ACCORDING TO THE ALTERNATE PATHWAY BY GLASS AND PLASTIC SURFACES AND ITS ROLE IN NEUTROPHIL ADHESION [J].
HED, J ;
JOHANSSON, M ;
LINDROTH, M .
IMMUNOLOGY LETTERS, 1984, 8 (06) :295-299
[36]   CRIg: A macrophage complement receptor required for phagocytosis of circulating pathogens [J].
Helmy, KY ;
Katschke, KJ ;
Gorgani, NN ;
Elliott, JM ;
Diehl, L ;
Scales, SJ ;
Ghilardi, N ;
Campagne, MV .
CELL, 2006, 124 (05) :915-927
[37]  
Higgins PJ, 1997, J IMMUNOL, V158, P2872
[38]   Protection of erythrocytes from human complement-mediated lysis by membrane-targeted recombinant soluble CD59: a new approach to PNH therapy [J].
Hill, A ;
Ridley, SH ;
Esser, D ;
Oldroyd, RG ;
Cullen, MJ ;
Kareclas, P ;
Gallagher, S ;
Smith, GP ;
Richards, SJ ;
White, J ;
Smith, RAG ;
Hillmen, P .
BLOOD, 2006, 107 (05) :2131-2137
[39]   The influence of cardiopulmonary bypass on cytokines and cell-cell communication [J].
Hill, GE ;
Whitten, CW ;
Landers, DF .
JOURNAL OF CARDIOTHORACIC AND VASCULAR ANESTHESIA, 1997, 11 (03) :367-375
[40]   A new in vitro model to study interaction between whole blood and biomaterials. Studies of platelet and coagulation activation acid the effect of aspirin [J].
Hong, J ;
Ekdahl, KN ;
Reynolds, H ;
Larsson, R ;
Nilsson, B .
BIOMATERIALS, 1999, 20 (07) :603-611