Traumatic Brain Injury
Conditions
Brief summary
Traumatic brain injuries (TBI) are one of the leading causes of death and disability worldwide. These patients are burdened by physical, cognitive, and psychosocial deficits, leading to an important economic impact for society. Treatments for TBI patients are limited and none has been shown to provide prolonged and long-term neuroprotective or neurorestorative effects. TBI related disability is linked to the severity of the initial injury but also to the following neuroinflammatory response which may persist long after the initial injury. Moreover, a growing body of evidence suggests a link between TBI-induced neuro-inflammation and neurodegenerative post traumatic disorders. Consequently, new therapies triggering immunomodulation and promoting neurological recovery are the subject of major research efforts. In this context, mesenchymal cell-based therapies are currently investigated to treat various neurological disorders due to their ability to modulate neuroinflammation and to promote simultaneous neurogenesis, angiogenesis, and neuroprotection. Clinical trials using intravenous MSC have been conducted for various pathologies, all these studies showing a good safety profile. The hypothesis of the study is that intravenous repeated treatment with MSC derived from Wharton's Jelly of the umbilical cord may be associated with a significant decrease of post-TBI neuroinflammation and improvement of neuroclinical status. The main objective of the study is to evaluate the effect of iterative IV injections of MSC on post-traumatic neuroinflammation measured in corpus callosum by PET-MRI at 6 months in severe brain injured patients unresponsive to simple verbal commands 5 days after sedation discontinuation.
Detailed description
Traumatic brain injuries (TBI) are one of the leading causes of death and disability worldwide. These patients are burdened by physical, cognitive, and psychosocial deficits, leading to an important economic impact for society. Treatments for TBI patients are limited and none has been shown to provide prolonged and long-term neuroprotective or neurorestorative effects. TBI related disability is linked to the severity of the initial injury but also to the following neuroinflammatory response which may persist long after the initial injury. Moreover, a growing body of evidence suggests a link between TBI-induced neuro-inflammation and neurodegenerative post traumatic disorders. Consequently, new therapies triggering immunomodulation and promoting neurological recovery are the subject of major research efforts. In this context, mesenchymal cell-based therapies are currently investigated to treat various neurological disorders due to their ability to modulate neuroinflammation and to promote simultaneous neurogenesis, angiogenesis, and neuroprotection. Indeed, several experimental studies have reported that human umbilical cord-derived mesenchymal stromal cells (MSC) have the ability to improve neurological outcomes and recovery in cerebral injury animal models, including TBI. Clinical trials using intravenous MSC have been conducted for various pathologies, all these studies showing a good safety profile. In TBI, small clinical trials using different modalities for administration of mesenchymal cells are available but none about MSC derived from Wharton's Jelly of the umbilical cord. The hypothesis of the study is that intravenous repeated treatment with MSC derived from Wharton's Jelly of the umbilical cord may be associated with a significant decrease of post-TBI neuroinflammation and improvement of neuroclinical status. The main objective of the study is to evaluate the effect of iterative IV injections of MSC on post-traumatic neuroinflammation measured in corpus callosum by PET-MRI at 6 months in severe brain injured patients unresponsive to simple verbal commands 5 days after sedation discontinuation.
Interventions
3 injections one week apart
3 injections one week apart
Sponsors
Study design
Masking description
use of placebo
Eligibility
Inclusion criteria
20 healthy volunteers will be included for MRI normalization Volunteer eligibility criteria Inclusion criteria : * Age 18-50 years * ASA 1 classification (healthy patient)
Exclusion criteria
: * Lack of written consent * Neurological history likely to alter the image (epilepsy, transient ischaemic attack, meningitis, head trauma) * Vulnerable person according to article L1121-6 of the CSP * Protected adult person * No affiliation to a social security regime * Pregnancy * Contraindication for MRI and PET-MRI * patients with Pacemaker and defibrillator * MR-incompatible prosthetic heart valve * Metallic intraocular, intra cerebral or intra medullary foreign bodies * Implantable neurostimulation systems * Cochlear implants/ear implant * Metallic fragments such as bullets, shotgun pellets, and metal shrapnel * Cerebral artery aneurysm clips * Ventriculo peritoneal shunt with metallic component generating significant artefacts on the MR sequence * Catheters with metallic components (Swan-Ganz catheter) * Patient unable to remain supine and motionless during the duration of the examination 68 severe TBI patients with the following inclusion and
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| effect of iterative IV injections of WJ-UC-MSC on post-traumatic neuroinflammation | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in corpus callosum (Region of Interest, ROI) measured by dynamic PET-MRI |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| long term Tolerance M12 | 6 months after the last injection | Common Terminology Criteria for Adverse Events |
| neuroinflammation of thalamus | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in thalamus, |
| neuroinflammation of mesencephalus | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in mesencephalus |
| neuroinflammation of cerebellum | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in cerebellum |
| Cytokine and chemokine levels in plasma | 6 months after the last injection | Luminex magnetic beads technology |
| PBMC profile | 6 months after the last injection | High-dimensional characterization of immune reprogramming during the treatment by single-cell RNA-sequencing of PBMC. |
| Transcriptomics and regulatory epigenomics of circulating monocytes and lymphocytes 1. | 6 months after the last injection | H3K27ac |
| Transcriptomics and regulatory epigenomics of circulating monocytes and lymphocytes 2. | 6 months after the last injection | H3K4me3 |
| Transcriptomics and regulatory epigenomics of circulating monocytes and lymphocytes 3. | 6 months after the last injection | ChIP-seq |
| Transcriptomics and regulatory epigenomics of circulating monocytes and lymphocytes 4. | 6 months after the last injection | ATAC-seq |
| Genome-wide single-nucleotide polymorphism (SNP) genotype. | After 1 injection | DNA sample |
| radiological markers from PET-MRI_1 | 6 months after the last injection | The regional fractional anisotropy (FA) from DTI acquisition of PET-MRI |
| radiological markers from PET-MRI_2 | 6 months after the last injection | The mean diffusibility (MD) from DTI acquisition of PET-MRI |
| Treatment feasibility | at the third injection | number of treatments administrated to the patient |
| Neurological clinical Score M6 | 6 months after the last injection | Glasgow Outcome Scale-Extended |
| Neurological clinical Score M12 | 12 months after the last injection | Glasgow Outcome Scale-Extended |
| cognitive assessment M6 | 6 months after the last injection | MOCA scale |
| cognitive assessment M12 | 12 months after the last injection | MOCA scale |
| short term Tolerance D10 | 10 days after the last injection | Common Terminology Criteria for Adverse Events |
| long term Tolerance M6 | 6 months after the last injection | Common Terminology Criteria for Adverse Events |
| neuroinflammation of pericontusional | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in pericontusional |
| neuroinflammation of grey matter | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in grey matter |
| neuroinflammation of white matter | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in white matter |
| neuroinflammation of frontal area | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in frontal area |
| neuroinflammation of parietal area | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in parietal area |
| neuroinflammation of occipital area | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in occipital area |
| neuroinflammation of hippocampus | 6 months after the last injection | \[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in hippocampus, |
Other
| Measure | Time frame | Description |
|---|---|---|
| Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration. 1 | After 3rd injection 48 hours later | populations of immune effector cells, such as Tregs, |
| Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration.2 | After 3rd injection 48 hours later | populations of immune effector cells, such as Teff, |
| Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration.3 | After 3rd injection 48 hours later | populations of immune effector cells, such as NK cells, |
| Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration. 4 | After 3rd injection 48 hours later | populations of immune effector cells, such as NKT, |
| Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration. 5 | After 3rd injection 48 hours later | populations of immune effector cells, such as MAIT, |
| Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration. 6 | After 3rd injection 48 hours later | populations of immune effector cells, such as DC |
| Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration. 7 | After 3rd injection 48 hours later | populations of immune effector cells, such as monocytes |
| Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration. 8 | After 3rd injection 48 hours later | populations of immune effector cells, such as B cells. |
| Analyze the pharmacokinetics and pharmacodynamics of CSM WJ-UC in humans 2 | After 3rd injection 48 hours later | digital droplet (dd)-PCR approach, |
| Analyze the pharmacokinetics and pharmacodynamics of CSM WJ-UC in humans 1 | After 3rd injection 48 hours later | NGS approach, |
Countries
France