Orthopaedic implant failure: aseptic implant loosening - the contribution and future challenges of mouse models in translational research

被引:50
作者
Cordova, Luis Alberto [1 ,2 ,3 ]
Stresing, Verena [1 ,2 ]
Gobin, Berengere [1 ,2 ]
Rosset, Philippe [1 ,2 ,4 ]
Passuti, Norbert [1 ,2 ,5 ]
Gouin, Francois [1 ,2 ,5 ]
Trichept, Valerie [1 ,2 ]
Layrolle, Pierre [1 ,2 ]
Feymann, Dominique [1 ,2 ,5 ]
机构
[1] INSERM, Fac Med, UMR 957, 1 Rue Gaston Veil, F-44035 Nantes 1, France
[2] Univ Nantes, Nantes Atlantique Univ, Lab Pathophysiol Bone Resorpt & Therapy Primary, F-44035 Nantes 1, France
[3] Univ Chile CONICYT, Fac Dent, Dept Oral & Maxillofacial Surg, Santiago, Chile
[4] Univ Tours, Tours Univ Hosp, F-37020 Tours, France
[5] Nantes Univ Hosp, Nantes 1, France
关键词
mouse model; orthopaedic implant; particle; periprosthetic osteolysis; polyethylene; wear debris; TOTAL HIP-ARTHROPLASTY; PARTICLE-INDUCED OSTEOLYSIS; INDUCED INFLAMMATORY OSTEOLYSIS; POLYETHYLENE WEAR PARTICLES; CROSS-LINKED POLYETHYLENE; INNATE IMMUNE-RESPONSE; VIL-10; GENE-TRANSFER; TOLL-LIKE RECEPTORS; MURINE MODEL; IN-VIVO;
D O I
10.1042/CS20130338
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aseptic loosening as a result of wear debris is considered to be the main cause of long-term implant failure in orthopaedic surgery and improved biomaterials for bearing surfaces decreases significantly the release of micrometric wear particles. Increasingly, in-depth knowledge of osteoimmunology highlights the role of nanoparticles and ions released from some of these new bearing couples, opening up a new era in the comprehension of aseptic loosening. Mouse models have been essential in the progress made in the early comprehension of pathophysiology and in testing new therapeutic agents for particle-induced osteolysis. However, despite this encouraging progress, there is still no valid clinical alternative to revision surgery. The present review provides an update of the most commonly used bearing couples, the current concepts regarding particle cell interactions and the approaches used to study the biology of periprosthetic osteolysis. It also discusses the contribution and future challenges of mouse models for successful translation of the preclinical progress into clinical applications.
引用
收藏
页码:277 / 293
页数:17
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