Focal lesions following intracerebral gene therapy for mucopolysaccharidosis IIIA

Abstract

Objective Mucopolysaccharidosis type IIIA (MPSIIIA) caused by recessive SGSH variants results in sulfamidase deficiency, leading to neurocognitive decline and death. No disease‐modifying therapy is available. The AAVance gene therapy trial investigates AAVrh.10 overexpressing human sulfamidase (LYS‐SAF302) delivered by intracerebral injection in children with MPSIIIA. Post‐treatment MRI monitoring revealed lesions around injection sites. Investigations were initiated in one patient to determine the cause. Methods Clinical and MRI details were reviewed. Stereotactic needle biopsies of a lesion were performed; blood and CSF were sampled. All samples were used for viral studies. Immunohistochemistry, electron microscopy, and transcriptome analysis were performed on brain tissue of the patient and various controls. Results MRI revealed focal lesions around injection sites with onset from 3 months after therapy, progression until 7 months post therapy with subsequent stabilization and some regression. The patient had transient slight neurological signs and is following near‐normal development. No evidence of viral or immunological/inflammatory cause was found. Immunohistochemistry showed immature oligodendrocytes and astrocytes, oligodendrocyte apoptosis, strong intracellular and extracellular sulfamidase expression and hardly detectable intracellular or extracellular heparan sulfate. No activation of the unfolded protein response was found. Interpretation Results suggest that intracerebral gene therapy with local sulfamidase overexpression leads to dysfunction of transduced cells close to injection sites, with extracellular spilling of lysosomal enzymes. This alters extracellular matrix composition, depletes heparan sulfate, impairs astrocyte and oligodendrocyte function, and causes cystic white matter degeneration at the site of highest gene expression. The AAVance trial results will reveal the potential benefit–risk ratio of this therapy.

Delivery of Adeno-Associated Virus Vectors to the Central Nervous System for Correction of Single Gene Disorders

“…A brain biopsy of one of the lesions showed no abundance of B or T cells, strong expression of transgene (sulfamidase), and no detectable heparan sulfate. The authors interpreted these results as an overexpression of sulfamidase locally at the site of gene therapy, which caused dysfunction of transduced cells and extracellular spilling of lysosomal enzymes [62]. Another case of intracranial pathology was observed in an earlier clinical trial for metachromatic leukodystrophy (MLD), a lysosomal disease caused by a defect in the arylsulfatase A (ARSA) gene.…”

Gene and Cellular Therapies for Leukodystrophies

“…injections [110,111], as well as local injections into the brain parenchyma. Risks of local injections are related to the presence of excess levels of the therapeutic protein as observed in AAV.rh10 gene therapy for mucopolysaccharidosis type IIIA, since the highest vector concentration occurs around the injection site [112], or alternatively, local injections can result in poor biodistribution affecting efficacy.…”