Biological challenges for regeneration of the degenerated disc using cellular therapies

被引:19
作者
Bendtsen, Michael [1 ]
Bunger, Cody [1 ]
Colombier, Pauline [2 ,7 ]
Le Visage, Catherine [2 ]
Roberts, Sally [3 ,4 ]
Sakai, Daisuke [5 ]
Urban, Jill P. G. [6 ]
机构
[1] Aarhus Univ Hosp, Dept Orthopaed, Aarhus, Denmark
[2] Univ Nantes, INSERM UMR 1229, Regenerat Med & Skeleton, F-44035 Nantes, France
[3] Keele Univ, Robert Jones & Agnes Hunt Orthopaed Hosp, Spinal Studies, Oswestry, Shrops, England
[4] Keele Univ, Robert Jones & Agnes Hunt Orthopaed Hosp, ISTM, Oswestry, Shrops, England
[5] Tokai Univ Hosp, Dept Orthopaed, Tokyo, Japan
[6] Univ Oxford, Dept Physiol Anat & Genet, Oxford, England
[7] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
关键词
HUMAN INTERVERTEBRAL DISC; LOW-BACK-PAIN; TRANSFORAMINAL EPIDURAL ETANERCEPT; MESENCHYMAL STROMAL CELLS; ISSLS PRIZE WINNER; NUCLEUS PULPOSUS; PROGENITOR CELLS; DOUBLE-BLIND; LUMBAR DISC; TISSUE;
D O I
10.1080/17453674.2017.1297916
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Interest in the biology of the intervertebral disc has grown significantly over the past 2 decades, driven mainly by studies aimed at developing biological therapies for repairing degenerate discs (Alini et al. 2002, Sakai and Grad 2015). Most interest has focused on cellular therapies, where cells, capable of synthesizing appropriate disc tissue, are implanted into the damaged tissue to replace resident cells that have died or have acquired a degenerative phenotype. This appears to be an attractive strategy, and has led to a significant increase in information about disc cellular biology. It follows the approach used clinically for repairing damaged cartilage (Hunziker et al. 2015); however, cell therapy for the disc faces more obstacles than that for cartilage repair and has not yet entered routine clinical practice. In this review, we discuss some of the challenges in successful cellular repair of the disc. We first review the function, organization, and composition of a normal disc, outline the changes that occur in degeneration, and consider how these might influence function. We then summarize cell therapy approaches to repairing the disc in relation to the choice of cells and cell support. We outline the challenges facing the implanted cells in the degenerate disc, and ask whether these therapies can be evaluated in animal models. Finally, we outline the important, but often neglected, problem of patient selection.
引用
收藏
页码:39 / 46
页数:8
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