Autologous bone marrow mononuclear cells to treat severe traumatic brain injury in children.
Charles S CoxDavid M NotricaJenifer JuranekJeffrey H MillerFabio TrioloSteven KosmachSean I SavitzP David AdelsonClaudia PedrozaScott D OlsonM Collins ScottAkshita KumarBenjamin M AertkerHenry W CaplanMargaret L JacksonBrijesh S GillRobert A HetzMichael S LavoieLinda Ewing-CobbsPublished in: Brain : a journal of neurology (2024)
Autologous bone marrow mononuclear cells (BMMNCs) infused after severe traumatic brain injury have shown promise for treating the injury. We evaluated their impact in children, particularly their hypothesized ability to preserve the blood-brain barrier and diminish neuroinflammation, leading to structural CNS preservation with improved outcomes. We performed a randomized, double-blind, placebo-sham-controlled Bayesian dose-escalation clinical trial at two children's hospitals in Houston, TX and Phoenix, AZ, USA (NCT01851083). Patients 5-17 years of age with severe traumatic brain injury (Glasgow Coma Scale score ≤ 8) were randomized to BMMNC or placebo (3:2). Bone marrow harvest, cell isolation and infusion were completed by 48 h post-injury. A Bayesian continuous reassessment method was used with cohorts of size 3 in the BMMNC group to choose the safest between two doses. Primary end points were quantitative brain volumes using MRI and microstructural integrity of the corpus callosum (diffusivity and oedema measurements) at 6 months and 12 months. Long-term functional outcomes and ventilator days, intracranial pressure monitoring days, intensive care unit days and therapeutic intensity measures were compared between groups. Forty-seven patients were randomized, with 37 completing 1-year follow-up (23 BMMNC, 14 placebo). BMMNC treatment was associated with an almost 3-day (23%) reduction in ventilator days, 1-day (16%) reduction in intracranial pressure monitoring days and 3-day (14%) reduction in intensive care unit (ICU) days. White matter volume at 1 year in the BMMNC group was significantly preserved compared to placebo [decrease of 19 891 versus 40 491, respectively; mean difference of -20 600, 95% confidence interval (CI): -35 868 to -5332; P = 0.01], and the number of corpus callosum streamlines was reduced more in placebo than BMMNC, supporting evidence of preserved corpus callosum connectivity in the treated groups (-431 streamlines placebo versus -37 streamlines BMMNC; mean difference of -394, 95% CI: -803 to 15; P = 0.055), but this did not reach statistical significance due to high variability. We conclude that autologous BMMNC infusion in children within 48 h after severe traumatic brain injury is safe and feasible. Our data show that BMMNC infusion led to: (i) shorter intensive care duration and decreased ICU intensity; (ii) white matter structural preservation; and (iii) enhanced corpus callosum connectivity and improved microstructural metrics.
Keyphrases
- double blind
- severe traumatic brain injury
- white matter
- bone marrow
- placebo controlled
- intensive care unit
- clinical trial
- phase iii
- traumatic brain injury
- mechanical ventilation
- young adults
- open label
- multiple sclerosis
- phase ii
- mesenchymal stem cells
- newly diagnosed
- induced apoptosis
- cell therapy
- study protocol
- ejection fraction
- healthcare
- magnetic resonance imaging
- acute respiratory distress syndrome
- type diabetes
- computed tomography
- magnetic resonance
- high intensity
- metabolic syndrome
- lipopolysaccharide induced
- stem cells
- electronic health record
- cell cycle arrest
- blood brain barrier
- machine learning
- randomized controlled trial
- inflammatory response
- oxidative stress
- weight loss
- cognitive impairment
- skeletal muscle
- cell proliferation