Does endotoxin contribute to aseptic loosening of orthopedic implants?

被引:107
作者
Greenfield, EM
Bi, YM
Ragab, AA
Goldberg, VM
Nalepka, JL
Seabold, JM
机构
[1] Case Western Reserve Univ, Univ Hosp Cleveland, Dept Orthopaed, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Pathol, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Physiol & Biophys, Cleveland, OH 44106 USA
关键词
aseptic loosening; endotoxin; lipopolysaccharide; osteoclast; osteolysis;
D O I
10.1002/jbm.b.30150
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Aseptic loosening of orthopedic implants caused by wear particles is a major clinical problem. This review examines the hypothesis that bacterial endotoxin contributes to aseptic loosening. Clinical findings support this hypothesis: bacterial biofilms exist on many implants from patients with aseptic loosening and antibiotics in bone cement reduce the rate of aseptic loosening. Three approaches were used to demonstrate that adherent endotoxin increases bioactivity of titanium particles. These experiments measured cytokine production and osteoclast differentiation in vitro and murine calvarial osteollysis in vivo. First, removal of > 99.9 % of the adherent endotoxin from titanium particles significantly ablates their biological activity. Second, adding lipopolysaccharide back to these "endotoxin-free" particles restores their biological activity. Third, cells or mice that are genetically hyporesponsive to endotoxin are significantly less responsive to titanium particles than are wild-type controls. Other investigators have confirmed and extended these results to include virtually all orthopedically relevant types of particles, including authentic titanium alloy particles retrieved from patients with loosening. Our recent studies suggest that adherent endotoxin on orthopedic implants may also inhibit initial osseointegration of the implants. Taken together, these studies suggest that bacterial endotoxin may have a significant role in induction of aseptic loosening. (C) 2004 Wiley, Periodicals. Inc.
引用
收藏
页码:179 / 185
页数:7
相关论文
共 84 条
[1]
The effect of particle wear debris on NFκB activation and pro-inflammatory cytokine release in differentiated THP-1 cells [J].
Akisue, T ;
Bauer, TW ;
Farver, CF ;
Mochida, Y .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 59 (03) :507-515
[2]
The effects of particulate cobalt, chromium and cobalt-chromium alloy on human osteoblast-like cells in vitro [J].
Allen, MJ ;
Myer, BJ ;
Millett, PJ ;
Rushton, N .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1997, 79B (03) :475-482
[3]
The prevention of prosthetic infection using a cross-linked albumin coating in a rabbit model [J].
An, YH ;
Bradley, J ;
Powers, DL ;
Friedman, RJ .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1997, 79B (05) :816-819
[4]
Periprosthetic bone resorption - Particles versus movement [J].
Aspenberg, P ;
Herbertsson, P .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1996, 78B (04) :641-646
[5]
The effects of degree of crosslinking on the fatigue crack initiation and propagation resistance of orthopedic-grade polyethylene [J].
Baker, DA ;
Bellare, A ;
Pruitt, L .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2003, 66A (01) :146-154
[6]
Bone ingrowth in the presence of particulate polyethylene - Synergy between interface motion and particulate polyethylene in periprosthetic tissue response [J].
Bechtold, JE ;
Kubic, V ;
Soballe, K .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2002, 84B (06) :915-919
[7]
Adherent endotoxin on orthopedic wear particles stimulates cytokine production and osteoclast differentiation [J].
Bi, YM ;
Seabold, JM ;
Kaar, SG ;
Ragab, AA ;
Goldberg, VM ;
Anderson, JM ;
Greenfield, EM .
JOURNAL OF BONE AND MINERAL RESEARCH, 2001, 16 (11) :2082-2091
[8]
Adherent endotoxin mediates biological responses of titanium particles without stimulating their phagocytosis [J].
Bi, YM ;
Collier, TO ;
Goldberg, VM ;
Anderson, JM ;
Greenfield, EM .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2002, 20 (04) :696-703
[9]
Titanium particles stimulate bone resorption by inducing differentiation of murine osteoclasts [J].
Bi, YM ;
Van de Motter, RR ;
Ragab, AA ;
Goldberg, VM ;
Anderson, JM ;
Greenfield, EM .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2001, 83A (04) :501-508
[10]
BLOEBAUM RD, 2003, T ORTHOP RES SOC, V28, P1345