Why the study?
There are no reported cases of patients with spinal muscular atrophy and severe hematological abnormalities who received onasemnogene abeparvovec gene therapy.
Is onasemnogene abeparvovec safe and effective in an infant with SMA type 1 and severe neutropenia?
Is onasemnogene abeparvovec safe and effective in an infant with SMA type 1 and severe neutropenia?
Onasemnogene abeparvovec was safely administered to an infant with SMA type 1 and severe neutropenia, resulting in neurological improvement and resolution of neutropenia.
Spinal muscular atrophy (SMA) is an autosomal recessive, neurodegenerative disorder resulting in severe, progressive hypotonia and muscular weakness. Spinal muscular atrophy is a multisystem disease, however limited information is available regarding its effect on the immune system, bone marrow and the myeloid cell development and function. Currently, three disease-modifying treatments that increase survival motor neuron (SMN) protein expression are available. Among them onasemnogene abeparvovec, an adeno-associated virus-based gene replacement therapy, delivers functional human SMN by a single-dose intravenous infusion and transient transaminasemia is the most significant adverse event. There are no reported cases of patients with SMA and severe hematological abnormalities who received the specific gene therapy. We describe a 10-month-old boy with SMA type 1 and severe neutropenia who was successfully administered onasemnogene abeparvovec, focusing on the investigational and post-treatment challenges as well as his outcome. The treatment was tolerated well, the patient showed neurological improvement and neutropenia resolved confirming the diagnosis of chronic benign neutropenia.
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Moutafi et al. (2025) studied this question.
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