椎间盘退变生物治疗进展(英文)

第一作者:石志远 

2012-05-18 点击量:967   我要说

石志远 张超 阮狄克

 With the continuous exploration of basic research for the pathogeny of intervertebral disc degenerative disease, the causes of intervertebral disc degeneration (the anabolic imbalance initiated by cells, extracellular matrix, growth factors and inflammatory factors) have gradually become explicit. Combining with the ceaseless extending of tissue engineering in the field of orthopedics, more and more clinical and basic researchers attempt to treat the discogenic disease through the exogenous interference in the process of intervertebral disc degeneration, including molecular therapy, cell therapy and gene therapy. In molecular therapy, stimulating endogenous cell activity and delaying the process of intervertebral disc degeneration, researchers attempt to increase the anabolic growth factors through reducing the inflammatory factors such as TNF-a, IL-8 and so on. Exogenous growth factors BMP7, BMP2 and BM14 (GDF5) have also been proved to have the effects of restraining intervertebral disc degeneration. In cell therapy, the researches are mainly on the introduction of exogenous cells and the expansion and replantation of autologous nucleus pulposus cells in vitro. A randomized controlled trial in clinic preliminarily confirms that the transplantation of autologous nucleus pulposus cells plays a role in maintaining the water content in the discs and the matrix content of nucleus pulposus. Gene therapy overcomes the side effects of the exogenous application of the growth factors and inhibition of inflammatory factors, but it has such defects as short-term effects, instability and so on. It gradually becomes the hot point, to which the researchers pay close attention. However, gene therapy should be performed under strict safety guarantee. The successful construction of a novel regulatory system structured by adenos viruses provides a powerful guarantee for the safety of gene therapy. As the carriers of cells, factors and genes, scaffold materials are indispensable in biological therapy. However, the pathogenic mechanism of the intervertebral disc degeneration has not been completely clear, which makes the biological therapy lack of a definite object. Then how to break through the bottlenecks of the biological therapy depends on the further confirmation of the mechanism of the intervertebral disc degeneration. It is also the field that should be focused on and explored by researchers.
 

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