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      First-in-human trial of blood–brain barrier opening in amyotrophic lateral sclerosis using MR-guided focused ultrasound

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          Abstract

          MR-guided focused ultrasound (MRgFUS) is an emerging technology that can accurately and transiently permeabilize the blood-brain barrier (BBB) for targeted drug delivery to the central nervous system. We conducted a single-arm, first-in-human trial to investigate the safety and feasibility of MRgFUS-induced BBB opening in eloquent primary motor cortex in four volunteers with amyotrophic lateral sclerosis (ALS). Here, we show successful BBB opening using MRgFUS as demonstrated by gadolinium leakage at the target site immediately after sonication in all subjects, which normalized 24 hours later. The procedure was well-tolerated with no serious clinical, radiologic or electroencephalographic adverse events. This study demonstrates that non-invasive BBB permeabilization over the motor cortex using MRgFUS is safe, feasible, and reversible in ALS subjects. In future, MRgFUS can be coupled with promising therapeutics providing a targeted delivery platform in ALS.

          Abstract

          MR-focused ultrasound can be used to transiently open the blood-brain barrier (BBB). Here, the authors report the results of a first-in-human trial on four patients with amyotrophic lateral sclerosis (ALS), showing that the procedure reversibly permeabilised the BBB in the motor cortex without complications, and suggest that the procedure could in the future be used to increase drug delivery in ALS patients.

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          Most cited references34

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          Clinical trial of blood-brain barrier disruption by pulsed ultrasound.

          The blood-brain barrier (BBB) limits the delivery of systemically administered drugs to the brain. Methods to circumvent the BBB have been developed, but none are used in standard clinical practice. The lack of adoption of existing methods is due to procedural invasiveness, serious adverse effects, and the complications associated with performing such techniques coincident with repeated drug administration, which is customary in chemotherapeutic protocols. Pulsed ultrasound, a method for disrupting the BBB, was shown to effectively increase drug concentrations and to slow tumor growth in preclinical studies. We now report the interim results of an ultrasound dose-escalating phase 1/2a clinical trial using an implantable ultrasound device system, SonoCloud, before treatment with carboplatin in patients with recurrent glioblastoma (GBM). The BBB of each patient was disrupted monthly using pulsed ultrasound in combination with systemically injected microbubbles. Contrast-enhanced magnetic resonance imaging (MRI) indicated that the BBB was disrupted at acoustic pressure levels up to 1.1 megapascals without detectable adverse effects on radiologic (MRI) or clinical examination. Our preliminary findings indicate that repeated opening of the BBB using our pulsed ultrasound system, in combination with systemic microbubble injection, is safe and well tolerated in patients with recurrent GBM and has the potential to optimize chemotherapy delivery in the brain.
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            The "dying-back" phenomenon of motor neurons in ALS.

            Amyotrophic lateral sclerosis (ALS) is a lethal disease, characterized by progressive death of motor neurons with unknown etiology. Evidence from animal models indicates that neuronal dysfunction precedes the clinical phase of the disease. However, in parallel extensive nerve sprouting and synaptic remodeling as part of a compensatory reinnervation processes and possibly also of motor neurons pathology was demonstrated. Therefore, the weakness in muscle groups will not be clinically apparent until a large proportion of motor units are lost. This motor unit loss and associated muscle function which precedes the death of motor neurons may resemble the "die-back" phenomena. Studies indicated that in the early stages the nerve terminals and motor neuron junctions are partially degraded while the cell bodies in the spinal cord are mostly intact. Treatments to rescue motor neurons according to "dying-forward" model of motor neuron pathology in ALS have shown only limited success in SOD1(G93A) transgenic mice as well as in humans. If cell body degeneration is late compared with axonal degeneration, early intervention could potentially prevent loss of motor neurons. Therefore, it should be considered, according to the dying back hypothesis, to focus on motor neurons terminals in order to delay or prevent the progressive degradation.
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              Targeted Delivery of Neural Stem Cells to the Brain Using MRI-Guided Focused Ultrasound to Disrupt the Blood-Brain Barrier

              Stem cell therapy is a promising strategy to treat neurodegenerative diseases, traumatic brain injury, and stroke. For stem cells to progress towards clinical use, the risks associated with invasive intracranial surgery used to deliver the cells to the brain, needs to be reduced. Here, we show that MRI-guided focused ultrasound (MRIgFUS) is a novel method for non-invasive delivery of stem cells from the blood to the brain by opening the blood brain barrier (BBB) in specific brain regions. We used MRI guidance to target the ultrasound beam thereby delivering the iron-labeled, green fluorescent protein (GFP)-expressing neural stem cells specifically to the striatum and the hippocampus of the rat brain. Detection of cellular iron using MRI established that the cells crossed the BBB to enter the brain. After sacrifice, 24 hours later, immunohistochemical analysis confirmed the presence of GFP-positive cells in the targeted brain regions. We determined that the neural stem cells expressed common stem cell markers (nestin and polysialic acid) suggesting they survived after transplantation with MRIgFUS. Furthermore, delivered stem cells expressed doublecortin in vivo indicating the stem cells were capable of differentiating into neurons. Together, we demonstrate that transient opening of the BBB with MRIgFUS is sufficient for transplantation of stem cells from the blood to targeted brain structures. These results suggest that MRIgFUS may be an effective alternative to invasive intracranial surgery for stem cell transplantation.
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                Author and article information

                Contributors
                agessandro.abrahao@sunnybrook.ca
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                26 September 2019
                26 September 2019
                2019
                : 10
                : 4373
                Affiliations
                [1 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Division of Neurology, Department of Medicine, Sunnybrook Health Sciences Centre, , University of Toronto, ; Toronto, ON M4N 3M5 Canada
                [2 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Hurvitz Brain Sciences Research Program, Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, , University of Toronto, ; Toronto, ON M4N 3M5 Canada
                [3 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Harquail Centre for Neuromodulation, , Sunnybrook Research Institute, ; Toronto, ON M4N 3M5 Canada
                [4 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Division of Neurosurgery, Sunnybrook Health Sciences Centre, , University of Toronto, ; Toronto, ON M4N 3M5 Canada
                [5 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, , University of Toronto, ; Toronto, ON M4N 3M5 Canada
                [6 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Department of Laboratory Medicine and Pathobiology, , University of Toronto, ; Toronto, ON M5S 3H7 Canada
                [7 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Department of Medical Imaging, Sunnybrook Health Sciences Centre, , University of Toronto, ; Toronto, ON M4N 3M5 Canada
                [8 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Odette Cancer Research, Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, , University of Toronto, ; Toronto, ON M4N 3M5 Canada
                [9 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Institute of Biomaterials and Biomedical Engineering, , University of Toronto, ; Toronto, ON M5S 3H7 Canada
                [10 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, Department of Medical Biophysics, , University of Toronto, ; Toronto, ON M5S 3H7 Canada
                Author information
                http://orcid.org/0000-0003-1142-2842
                http://orcid.org/0000-0001-5163-9961
                http://orcid.org/0000-0001-7093-8289
                Article
                12426
                10.1038/s41467-019-12426-9
                6763482
                31558719
                da75eef4-b429-4f7a-9f90-ad10142bbe8c
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 8 February 2019
                : 6 September 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/100009017, ALS Society of Canada (ALS Canada);
                Categories
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                Custom metadata
                © The Author(s) 2019

                Uncategorized
                blood-brain barrier,brain,amyotrophic lateral sclerosis
                Uncategorized
                blood-brain barrier, brain, amyotrophic lateral sclerosis

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