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Effects of Intravascular Administration of Mesenchymal Stromal Cells Derived from Wharton's Jelly of the Umbilical Cord on Systemic Immunomodulation and Neuroinflammation After Traumatic Brain Injury.

Effects of Intravascular Administration of Mesenchymal Stromal Cells Derived from Wharton's Jelly of the Umbilical Cord on Systemic Immunomodulation and Neuroinflammation After Traumatic Brain Injury.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06146062
Acronym
TRAUMACELL
Enrollment
68
Registered
2023-11-24
Start date
2024-06-25
Completion date
2028-03-31
Last updated
2024-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Traumatic Brain Injury

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

DRUGMesenchymal Stromal Cells (MSC)

3 injections one week apart

DRUGplacebo

3 injections one week apart

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

use of placebo

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

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

MeasureTime frameDescription
effect of iterative IV injections of WJ-UC-MSC on post-traumatic neuroinflammation6 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

MeasureTime frameDescription
long term Tolerance M126 months after the last injectionCommon Terminology Criteria for Adverse Events
neuroinflammation of thalamus6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in thalamus,
neuroinflammation of mesencephalus6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in mesencephalus
neuroinflammation of cerebellum6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in cerebellum
Cytokine and chemokine levels in plasma6 months after the last injectionLuminex magnetic beads technology
PBMC profile6 months after the last injectionHigh-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 injectionH3K27ac
Transcriptomics and regulatory epigenomics of circulating monocytes and lymphocytes 2.6 months after the last injectionH3K4me3
Transcriptomics and regulatory epigenomics of circulating monocytes and lymphocytes 3.6 months after the last injectionChIP-seq
Transcriptomics and regulatory epigenomics of circulating monocytes and lymphocytes 4.6 months after the last injectionATAC-seq
Genome-wide single-nucleotide polymorphism (SNP) genotype.After 1 injectionDNA sample
radiological markers from PET-MRI_16 months after the last injectionThe regional fractional anisotropy (FA) from DTI acquisition of PET-MRI
radiological markers from PET-MRI_26 months after the last injectionThe mean diffusibility (MD) from DTI acquisition of PET-MRI
Treatment feasibilityat the third injectionnumber of treatments administrated to the patient
Neurological clinical Score M66 months after the last injectionGlasgow Outcome Scale-Extended
Neurological clinical Score M1212 months after the last injectionGlasgow Outcome Scale-Extended
cognitive assessment M66 months after the last injectionMOCA scale
cognitive assessment M1212 months after the last injectionMOCA scale
short term Tolerance D1010 days after the last injectionCommon Terminology Criteria for Adverse Events
long term Tolerance M66 months after the last injectionCommon Terminology Criteria for Adverse Events
neuroinflammation of pericontusional6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in pericontusional
neuroinflammation of grey matter6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in grey matter
neuroinflammation of white matter6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in white matter
neuroinflammation of frontal area6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in frontal area
neuroinflammation of parietal area6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in parietal area
neuroinflammation of occipital area6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in occipital area
neuroinflammation of hippocampus6 months after the last injection\[18F\]-DPA-714 Standard Uptake Value ratio (SUVr) in hippocampus,

Other

MeasureTime frameDescription
Deep phenotyping of the main immune effector cell populations humans, to identify the phenotypes involved in immunomodulation and alloimmunization induced by MSC administration. 1After 3rd injection 48 hours laterpopulations 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.2After 3rd injection 48 hours laterpopulations 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.3After 3rd injection 48 hours laterpopulations 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. 4After 3rd injection 48 hours laterpopulations 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. 5After 3rd injection 48 hours laterpopulations 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. 6After 3rd injection 48 hours laterpopulations 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. 7After 3rd injection 48 hours laterpopulations 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. 8After 3rd injection 48 hours laterpopulations of immune effector cells, such as B cells.
Analyze the pharmacokinetics and pharmacodynamics of CSM WJ-UC in humans 2After 3rd injection 48 hours laterdigital droplet (dd)-PCR approach,
Analyze the pharmacokinetics and pharmacodynamics of CSM WJ-UC in humans 1After 3rd injection 48 hours laterNGS approach,

Countries

France

Contacts

Primary ContactVincent Degos
vincent.degos@aphp.fr142163761
Backup ContactStéphanie Sigaut
stephanie.sigaut@aphp.fr140875009

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026