The Role of Instrumentation in the Healing Process of Spinal Tuberculosis: An Experimental Study
DOI:
https://doi.org/10.3889/oamjms.2021.6065Keywords:
Transforming growth factor-beta, Spinal tuberculosis infection, Instrumentation, Cytokine expression, Healing processAbstract
Introduction: Tuberculosis is still commonly found in many developing countries. Spinal tuberculosis can cause vertebral deformity and neurological disorders. It was discovered thousands years ago and its management was aimed to eradicate infection and maintain the integrity of the vertebrae. Previously, the management of spinal TB was using drugs and external stabilization. Surgical techniques were developed afterwards to clean the infected vertebral segment. Because of the vertebral deformity remained inevitable and had impacts on neurological disorders, new paradigm had been developed by using instrumentation to stabilize the deformity of infected vertebral segment and to restore and maintain neurological function. TGF-β has a major role in angiogenesis in bone healing process. Spinal TB instrumentation uses metal devices composed of ions and particles that can interact each other so it could produce physical and chemical energy that is transmitted to the vertebrae. The energy is expected to enhance the biomolecular and biocellular activity of the body's immune cells so the healing process could be better.
Methods: An experimental study was carried out on New Zealand Rabbits which were given TB H37Rv strain infection in the vertebral body. Samples were divided into five groups namely control rabbits, infected rabbits without intervention, infected rabbits treated by instrumentation, infected rabbits given anti-tuberculosis drugs and infected rabbits treated by instrumentation and given drugs. Then the cytokine levels of TGF-β were evaluated and compared.
Results: The results showed a significant TGF- β level increase in infected rabbits given drugs alone and instrumentation alone compared to infected rabbits without intervention. There was a significant TGF- β increase in infected rabbits given drugs and treated by instrumentation compared to control rabbits and rabbits who received drugs only.
Conclusions: Instrumentation can improve the healing process in spinal tuberculosis by increasing the body's cytokine levels.
Downloads
Metrics
Plum Analytics Artifact Widget Block
References
Sharma D, Sarkar D. Pathophysiology of tuberculosis: An update review. PharmaTutor. 2018;6(2):15-21. DOI: https://doi.org/10.29161/PT.v6.i2.2018.15
World Health Organization. Global Tuberculosis Report; 2019. Available from: https://www.apps.who.int/iris/bitstream/handle/10665/329368/9789241565714-eng.pdf?ua=1. [Last accessed on 2020 Apr 10].
Rasouli MR, Mirkoohi M, Vaccaro AR, Yarandi KK, Rahimi-Movaghar V. Spinal tuberculosis: Diagnosis and management. Asian Spine J. 2012;6(4):294-308. https://doi.org/10.4184/asj.2012.6.4.294 PMid:23275816 DOI: https://doi.org/10.4184/asj.2012.6.4.294
Kaptigau WM, Koiri JB, Kevau IH, Rosenfeld JV. Surgical management of spinal tuberculosis in Papua new Guinea. P N G Med J. 2007;50(1-2):25-32.
Nataprawira HM, Ruslianti V, Solek P, Hawani D, Milanti M, Anggraeni R, et al. Outcome of tuberculous meningitis in children: The first comprehensive retrospective cohort study in Indonesia. Int J Tuberc Lung Dis. 2016;20(7):909-14. https://doi.org/10.5588/ijtld.15.0555 PMid:19354009 DOI: https://doi.org/10.5588/ijtld.15.0555
Agrawal V, Patgaonkar PR, Nagariya SP. Tuberculosis of spine. J Craniovertebr Junction Spine. 2010;1(2):74-85. https://doi.org/10.4103/0974-8237.77671 PMid:21572628 DOI: https://doi.org/10.4103/0974-8237.77671
Patil SS, Mohite S, Varma R, Bhojraj SY, Nene AM. Non-surgical management of cord compression in tuberculosis: A series of surprises. Asian Spine J. 2014;8(3):315-21. https://doi.org/10.4184/asj.2014.8.3.315 PMid:24967045 DOI: https://doi.org/10.4184/asj.2014.8.3.315
Jain AK, Jain S. Instrumented stabilization in spinal tuberculosis. Int Orthop J. 2012;36(2):285-92. https://doi.org/10.1007/s00264-011-1296-5 PMid:21720864 DOI: https://doi.org/10.1007/s00264-011-1296-5
Ghiasi MS, Chen J, Vaziri A, Rodriguez EK, Nazarian A. Bone fracture healing in mechanobiological modeling: A review of principles and methods. Bone Rep. 2017;6:87-100. https://doi.org/10.1016/j.bonr.2017.03.002 PMid:28377988 DOI: https://doi.org/10.1016/j.bonr.2017.03.002
Korbel DS, Schneider BE, Schaible UE. Innate immunity in tuberculosis: Myths and truth. Microbes Infect. 2008;10(9):995-1004. https://doi.org/10.1016/j.micinf.2008.07.039 PMid:18762264 DOI: https://doi.org/10.1016/j.micinf.2008.07.039
Oga M, Arizono T, Takasita M, Sugioka Y. Evaluation of the risk of instrumentation as a foreign body in spinal tuberculosis. Clinical and biologic study. Spine J. 1993;18(13):1890-4. https://doi.org/10.1097/00007632-199310000-00028 PMid:8235878 DOI: https://doi.org/10.1097/00007632-199310000-00028
Gordon S, Taylor PR. Monocyte and macrophage heterogeneity. Nat Rev Immunol. 2005;5(12):953-64. https://doi.org/10.1038/nri1733 PMid:16322748 DOI: https://doi.org/10.1038/nri1733
Brancato SK, Albina JE. Wound macrophages as key regulators of repair: Origin, phenotype, and function. Am J Pathol. 2011;178(1):19-25. PMid:21224038 DOI: https://doi.org/10.1016/j.ajpath.2010.08.003
Novak ML, Koh TJ. Macrophage phenotypes during tissue repair. J Leukoc Biol. 2013;93(6):875-81. https://doi.org/10.1189/jlb.1012512 PMid:23505314 DOI: https://doi.org/10.1189/jlb.1012512
Arranz A, Doxaki C, Vergadi E, de la Torre YM, Vaporidi K, Lagoudaki ED, et al. Akt1 and Akt2 protein kinases differentially contribute to macrophage polarization. Proc Natl Acad Sci U S A. 2012;109(24):9517-22. https://doi.org/10.1073/pnas.1119038109 PMid:22647600 DOI: https://doi.org/10.1073/pnas.1119038109
Gordon S, Martinez FO. Alternative activation of macrophages: Mechanism and functions. Immunity. 2010;32(5):593-604. https://doi.org/10.1016/j.immuni.2010.05.007 PMid:20510870 DOI: https://doi.org/10.1016/j.immuni.2010.05.007
Mavrogenis AF, Dimitriou R, Parvizi J, Babis GC. Biology of implant osseointegration. J Musculoskelet Neuronal Interact. 2009;9(2):61-71. PMid:19516081
Han G, Shen Z. Microscopic view of osseointegration and functional mechanisms of implant surfaces. Mater Sci Eng C Mater Biol Appl. 2015;56:380-5. https://doi.org/10.1016/j.msec.2015.06.053 PMid:26249604 DOI: https://doi.org/10.1016/j.msec.2015.06.053
Brunetti G, Mori G, D’Amelio P, Faccio R. The crosstalk between the bone and the immune system: Osteoimmunology. Clin Dev Immunol. 2013;2013:617319. DOI: https://doi.org/10.1155/2013/617319
Crotti TN, Dharmapatni AA, Alias E, Haynes DR. Osteoimmunology: Major and costimulatory pathway expression associated with chronic inflammatory induced bone loss. J Immunol Res. 2015;2015:281287. https://doi.org/10.1155/2015/281287 PMid:26064999 DOI: https://doi.org/10.1155/2015/281287
Masuki H, Okudera T, Watanebe T. Growth factor and pro-inflammatory cytokine contents in platelet-rich plasma (PRP), plasma rich in growth factors (PRGF), advanced platelet-rich fibrin (A-PRF), and concentrated growth factors (CGF). Int J Implant Dent. 2016;2(1):19. https://doi.org/10.1186/s40729-016-0052-4 PMid:27747711 DOI: https://doi.org/10.1186/s40729-016-0052-4
Rutkovskiy A, Stensløkken KO, Vaage IJ. Osteoblast differentiation at a glance. Med Sci Monit Basic Res. 2016;22:95-106. https://doi.org/10.12659/msmbr.901142 PMid:27667570 DOI: https://doi.org/10.12659/MSMBR.901142
Park BS, Heo SJ, Kim CS, Oh JE, Kim JM, Lee G, et al. Effects of adhesion molecules on the behaviour of osteoblast-like cells and normal human fibroblast on different titanium surfaces. J Biomed Mater Res Part A. 2005;74(4):640-51. https://doi.org/10.1002/jbm.a.30326 PMid:16015642 DOI: https://doi.org/10.1002/jbm.a.30326
Yang Y, Cavin R, Ong JI. Protein adsorption on titanium surfaces and their effect on osteoblast attachment. J Biomed Mater Res Part A. 2003;67(1):344-9. https://doi.org/10.1002/jbm.a.10578 PMid:14517894 DOI: https://doi.org/10.1002/jbm.a.10578
Lee MH, Oh N, Lee SW, Leesungbok R, Kim SE, Yun YP, et al. Factors influencing osteoblast maturation on microgrooved titanium substrata. Biomaterials. 2010;31(14):3804-15. https://doi.org/10.1016/j.biomaterials.2010.01.117 PMid:20153892 DOI: https://doi.org/10.1016/j.biomaterials.2010.01.117
MacDonald DE, Deo N, Markovic B, Stranick M Somasundaran P. Thermal and Chemical modification of titanium-aluminium-vanadium implant materials: Effects on surface properties, glycoprotein adsorption, and MG63 cell attachment. Biomaterials. 2004;25(16):3135-46. https://doi.org/10.1016/j.biomaterials.2003.10.029 PMid:14980408 DOI: https://doi.org/10.1016/j.biomaterials.2003.10.029
Ruoslahti E. Rgd and other recognition sequences for integrins. Ann Rev Cell Dev Biol. 1996;12:697-715. https://doi.org/10.1146/annurev.cellbio.12.1.697 PMid:8970741 DOI: https://doi.org/10.1146/annurev.cellbio.12.1.697
Hynes RO. Integrins: Bidirectional, allosteric signalling machines. Cell. 2002;110(6):673-87. PMid:12297042 DOI: https://doi.org/10.1016/S0092-8674(02)00971-6
Downloads
Published
How to Cite
Issue
Section
Categories
License
Copyright (c) 2020 Tjuk Risantoso, Mohammad Hidayat, Hidayat Suyuti, Aulani Niam (Author)

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
http://creativecommons.org/licenses/by-nc/4.0