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Intranasal Human-Recombinant Nerve Growth Factor Enhances Motor and Cognitive Function Recovery in a Child with
Lorenzo Di Sarno1, Lavinia Capossela1, Serena Ferretti1
1Institute of Pediatrics, Fondazione Policlinico A. Gemelli IRCCS, 00168 Rome, Italy.
Insights
Intranasal nerve growth factor (NGF) shows promise for pediatric traumatic brain injury (TBI) recovery. A young boy with severe TBI experienced significant motor and cognitive improvements after receiving human-recombinant NGF (hr-NGF) intranasally.
Area of Science:
- Neuroscience
- Pediatric Neurology
- Regenerative Medicine
Background:
- Pediatric traumatic brain injury (TBI) causes significant mortality and morbidity, with limited regenerative therapies.
- The developing brain is vulnerable, potentially leading to long-term deficits.
- Nerve growth factor (NGF) shows potential for neuroprotection and recovery, with intranasal administration offering a non-invasive route.
Abstract:
Introduction: Traumatic brain injury (TBI) in pediatric population is responsible for significant mortality and morbidity, particularly among children aged 0-4 and young adults aged 15-24. The developing brain's unique characteristics may increase vulnerability to injuries, potentially leading to long-term cognitive and motor deficits. Current therapeutic options for neuronal regeneration post-TBI are limited, although neurotrophins, especially nerve growth factor (NGF), show promise in enhancing recovery. NGF can mitigate excitotoxicity and promote neuroprotection, particularly by intranasal administration, which is attractive because of its non-invasive nature. Case Presentation: A three-year-old boy suffered from severe TBI due to a car accident, leading to multiple complications, including a basilar skull fracture and cerebral venous sinus thrombosis. Initial assessments revealed significant neurological impairments. After intensive care and rehabilitation, the child exhibited gradual improvements in consciousness and motor functions but continued to face challenges, particularly with left-sided hemiparesis. Nine months post-injury, he began intranasal administration of human-recombinant NGF (hr-NGF) as part of a clinical trial. Discussion: Following hr-NGF treatment, the child demonstrated notable advancements in motor function, achieving independent standing and walking. Cognitive assessments indicated improvements in various domains, including verbal comprehension and executive functioning. EEG results showed reduced epileptiform activity. These findings suggest that hr-NGF may facilitate recovery in pediatric TBI cases by enhancing both motor and cognitive outcomes. Conclusions: This case highlights the potential role of intranasal hr-NGF administration as a therapeutic strategy for improving neurological recovery in children with severe TBI. The positive clinical outcomes support further exploration of NGF as a viable treatment option to mitigate long-term sequelae associated with pediatric brain injuries.
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