The researchers have already received further funding and are planning to develop an implantable device for use in humans with traumatic spinal cord injury.
Surgery after spinal cord injury is common. The concept could offer surgeons the opportunity during the same operation to implant a device which could help protect and repair the spinal cord itself.
Patients with spinal cord injury (SCI) could benefit from a future treatment to repair nerve connections using red and near-infrared light.
The method, invented by scientists at the University of Birmingham and patented by University of Birmingham Enterprise, involves delivering light directly to the site of the injury.
Their latest research, published today in the journal Bioengineering and Translational Medicine has determined an optimal ‘dose’ for this novel therapeutic approach, and shown that it can deliver significant therapeutic improvements including significant restoration of sensation and movement, and regeneration of damaged nerve cells.
Excitingly, this aspect of the study showed the effect of 660nm light was both neuroprotective, meaning it improved survival of nerve cells, and neuroregenerative, meaning it stimulated nerve cell growth.
Researchers led by Professor Zubair Ahmed used cell models of SCI to determine the frequency and duration of light required to achieve maximum restoration of function and stimulate nerve cell regrowth.
They found that delivery of red light at a wavelength of 660nm for one minute a day increased cell viability (a measurement of the number of live cells) by 45% over five days of treatment.
Professor Ahmed said: “Excitingly, this aspect of the study showed the effect of 660nm light was both neuroprotective, meaning it improved survival of nerve cells, and neuroregenerative, meaning it stimulated nerve cell growth.”
The researchers also investigated the effect of light therapy in preclinical models of SCI. Here they used two different methods, an implantable device and transcutaneous delivery, where the light source is placed against the skin. Their study showed comparable results for both delivery methods, with a one-minute dose of 660nm light, delivered daily for seven days, resulting in reduced tissue scarring at the site of injury, and significant functional recovery.
The researchers also found significant reductions in both cavities and scarring as well as increases in the levels of proteins associated with nerve cell regeneration and improvements in the connections between cells in the injured area of the spine.
This is the first time transcutaneous and direct delivery of light have been compared in SCI, and the results are a milestone for the researchers, who have already received further funding and are planning to develop an implantable device for use in humans with traumatic SCI, where there are currently no approaches that preserve cells or improve neurological function.
Surgery after spinal cord injury is common, but currently these operations are only aimed at stabilising injuries to the bones of the spine that have been damaged by the trauma. This concept is incredibly exciting as it could offer surgeons the opportunity during the same operation to implant a device which could help protect and repair the spinal cord itself.
Professor Ahmed continued: “To make light therapy viable for treating SCI in humans an implantable device will be required, to provide line of sight to damaged tissue and the opportunity for greater accuracy and standardise dosing without impedance due to the thickness of skin and other tissues surrounding the spinal cord.
Photobiomodulation (PBM) may provide a viable therapeutic approach using red or near-infrared light to promote recovery after SCI by mitigating neuroinflammation and preventing neuronal apoptosis. Our current study aimed to optimize PBM dose regimens and develop and validate the efficacy of an invasive PBM delivery paradigm for SCI.”
The research team is now seeking commercial partners or investors to take the next steps towards developing a prototype device that can be taken into first-in-man clinical trials.
In the study, the researchers are using a form of light therapy called photobiomodulation (PBM), which aims to improve healing and reduce inflammation. There is established evidence for its effectiveness in a wide variety of dermatological and oral applications, where metered light dosing can be achieved with precision in direct-to-tissue delivery. For example, PBM is already NICE-approved for oral mucositis, where it has been shown to reduce the debilitating ulcers and painful inflammation in the mouth caused by cancer treatments.
In the central nervous system, PBM has been widely studied in preclinical models of Parkinson’s disease, where it has been shown to be safe and effective. In SCI, PBM delivers its therapeutic benefit by mitigating the inflammation that follows injury, in nerve cells, macrophages (immune cells) and astrocytes.
PBM achieves these effects by working principally on mitochondria, which are photoactive and present in every cell in the body where they generate adenosine triphosphate (ATP) which is used within cells as a source of chemical energy. PBM increases the availability of ATP, and this triggers multiple pathways that mitigate apoptosis (cell death), neuronal damage and neuroinflammation and promote neuronal regeneration.
The implantable device was originally envisaged by neurosurgeon Mr David Davies, who works in the field of traumatic brain injury in the NIHR Surgical Reconstruction and Microbiology Research Centre, and photobiomodulation expert Professor Will Palin from Birmingham’s School of Dentistry. University of Birmingham Enterprise has patented the apparatus and methods for treating traumatic brain injury and traumatic spinal injury, and the research team involved with its development now includes Professor of Neuroscience, Zubair Ahmed and Clinical Research Fellow and Neurosurgery Registrar, Mr Andrew Stevens from Birmingham’s Institute of Inflammation and Ageing.
Photobiomodulation (PBM) may provide a viable therapeutic approach using red or near-infrared light to promote recovery after SCI by mitigating neuroinflammation and preventing neuronal apoptosis. Our current study aimed to optimize PBM dose regimens and develop and validate the efficacy of an invasive PBM delivery paradigm for use in human SCI.
Implantable and transcutaneous photobiomodulation promote neuroregeneration and recovery of lost function after spinal cord injury is published in Bioengineering & Translational Medicine, and available at https://doi.org/10.1002/btm2.10674
For media enquiries contact Ruth Ashton.
For commercial enquiries contact Dr Veemal Bhowruth.
Professor of Neuroscience
Staff profile for Professor Zubair Ahmed, Professor of Neuroscience, Department of Inflammation and Ageing, College of Medicine and Health.
Clinical Research Fellow
Staff profile for Mr Andrew Stevens, Clinical Research Fellow based in the Institute of Inflammation and Ageing, University of Birmingham.
Professor in Biomedical Materials Science
Will Palin staff profile
Professor of Trauma Neurosurgery
Staff profile for Professor Tony Belli, Professor of Trauma Neurosurgery, Institute of Inflammation and Ageing, College of Medical and Dental Sciences, the Unviersity of Birmingham
