BIOTECHNOLOGIES IN THE TREATMENT OF DEGENERATIVE DISC DISEASE OF THE CERVICAL SPINE

被引:1
作者
Ferdinandov, Dilyan [1 ]
Tsekov, Iliya [2 ]
Bussarsky, Ventzeslav [1 ]
Kalvatchev, Zlatko [3 ]
机构
[1] Med Univ Sofia, Dept Neurosurg, Sofia, Bulgaria
[2] Natl Ctr Infect & Parasit Dis, Dept Virol, Sofia, Bulgaria
[3] Mil Med Acad, Mol Virol Lab, Sofia, Bulgaria
关键词
degenerative disc disease; intervertebral disc; cervical spine; biotechnology; BONE MORPHOGENETIC PROTEIN-2; NUCLEUS PULPOSUS CELLS; INTERVERTEBRAL DISC; GENE-TRANSFER; IN-VIVO; PROTEOGLYCAN; FUSION; RABBIT; INHIBITION; DISKECTOMY;
D O I
10.5504/BBEQ.2011.0136
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Degenerative disc disease of the cervical spine is a common medical condition in the population with underlying aging, genetic, mechanical and environmental factors. It is characterized with structural collapse, osteophyte formation and loss of the loading function of the intervertebral disc. As a consequence a compression of neural structures is observed with axial neck pain, cervical radiculopathy and myelopathy. Currently, the cervical interbody fusion and artificial disc implantation are the available operative treatment options when medications and physiotherapy are ineffective. New strategies focusing on biologic modalities would be appealing. We review the advanced biotechnologies in the treatment of degenerative disc disease of the spine. Many studies are focused on therapeutic molecules capable to influence the biochemical and structural processes of intervertebral disc degeneration. These factors are categorized as anticatabolics, mitogens, chondrogenic morphogens and intracellular regulators. Another step that further opposes the simple injection of tissues with therapeutic molecules is gene therapy seeking to transfer genetic material into target cells, which in turn become in situ factories for the long-term production of desired proteins. The use of tissue-engineered intervertebral disc constructs may prove helpful when treating degenerative cervical disc disease. An in vitro technology designed to produce cartilage or bone with desired biomechanical properties to repair damaged tissues is available nowadays. In the near future the golden standard might be the replacement of the degenerated disc with biological rather than polymer or metal prostheses. However, the cost-effectiveness of the reviewed approaches has not been definitively established. Regardless of its efficacy, the safety and economic issues may ultimately determine whether these therapies are viewed as an acceptable alternative to the recent treatment options.
引用
收藏
页码:3132 / 3137
页数:6
相关论文
共 40 条
[1]  
AHN SH, 2003, SPINE J, V3, pS70
[2]   Percutaneous spinal fusion using bone morphogenetic protein-2 gene therapy [J].
Alden, TD ;
Pittman, DD ;
Beres, EJ ;
Hankins, GR ;
Kallmes, DF ;
Wisotsky, BM ;
Kerns, KM ;
Helm, GA .
JOURNAL OF NEUROSURGERY, 1999, 90 (01) :109-114
[3]   Intradiscal administration of osteogenic protein-1 increases intervertebral disc height and proteoglycan content in the nucleus pulposus in normal adolescent rabbits [J].
An, HS ;
Takegami, K ;
Kamada, H ;
Nguyen, CM ;
Thonar, EJMA ;
Singh, K ;
Andersson, GB ;
Masuda, K .
SPINE, 2005, 30 (01) :25-31
[4]   Anterior cervical discectomy and fusion involving a polyetheretherketone spacer and bone morphogenetic protein [J].
Boakye, M ;
Mummaneni, PV ;
Garrett, M ;
Rodts, G ;
Haid, R .
JOURNAL OF NEUROSURGERY-SPINE, 2005, 2 (05) :521-525
[5]   Transplantation of mesenchymal stem cells and nucleus pulposus cells in a degenerative disc model in rabbits: a comparison of 2 cell types as potential candidates for disc regeneration Laboratory investigation [J].
Feng, Ganjun ;
Zhao, Xianfeng ;
Liu, Hao ;
Zhang, Huina ;
Chen, Xiangjun ;
Shi, Rui ;
Liu, Xi ;
Zhao, Xiaodan ;
Zhang, Wenli ;
Wang, Beiyu .
JOURNAL OF NEUROSURGERY-SPINE, 2011, 14 (03) :322-329
[6]   Current understanding of cellular and molecular events in intervertebral disc degeneration: implications for therapy [J].
Freemont, AJ ;
Watkins, A ;
Le Maitre, C ;
Jeziorska, M ;
Hoyland, JA .
JOURNAL OF PATHOLOGY, 2002, 196 (04) :374-379
[7]   Cervical motion preservation using mesenchymal progenitor cells and pentosan polysulfate, a novel chondrogenic agent: preliminary study in an ovine model [J].
Goldschlager, Tony ;
Ghosh, Peter ;
Zannettino, Andrew ;
Gronthos, Stan ;
Rosenfeld, Jeffrey V. ;
Itescu, Silviu ;
Jenkin, Graham .
NEUROSURGICAL FOCUS, 2010, 28 (06) :1-8
[8]   Anti-apoptotic effects of IGF-1 and PDGF on human intervertebral disc cells in vitro [J].
Gruber, HE ;
Norton, HJ ;
Hanley, EN .
SPINE, 2000, 25 (17) :2153-2157
[9]   Smad signaling in mesenchymal and chondroprogenitor cells [J].
Hatakeyama, Y ;
Nguyen, J ;
Wang, XB ;
Nuckolls, GH ;
Shum, L .
JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 2003, 85A :13-18
[10]   Bone morphogenetic protein-2 facilitates expression of chondrogenic, not osteogenic, phenotype of human intervertebral disc cells [J].
Kim, DJ ;
Moon, SH ;
Kim, H ;
Kwon, UH ;
Park, MS ;
Han, KJ ;
Hahn, SB ;
Lee, HM .
SPINE, 2003, 28 (24) :2679-2684