{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,10]],"date-time":"2026-07-10T15:41:12Z","timestamp":1783698072021,"version":"3.55.0"},"reference-count":44,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2023,5,11]],"date-time":"2023-05-11T00:00:00Z","timestamp":1683763200000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Ann Clin Transl Neurol"],"published-print":{"date-parts":[[2023,6]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Objective<\/jats:title><jats:p>Mucopolysaccharidosis type IIIA (MPSIIIA) caused by recessive <jats:italic>SGSH<\/jats:italic> variants results in sulfamidase deficiency, leading to neurocognitive decline and death. No disease\u2010modifying therapy is available. The AAVance gene therapy trial investigates AAVrh.10 overexpressing human sulfamidase (LYS\u2010SAF302) delivered by intracerebral injection in children with MPSIIIA. Post\u2010treatment MRI monitoring revealed lesions around injection sites. Investigations were initiated in one patient to determine the cause.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>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.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>MRI revealed focal lesions around injection sites with onset from 3\u2009months after therapy, progression until 7\u2009months post therapy with subsequent stabilization and some regression. The patient had transient slight neurological signs and is following near\u2010normal 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.<\/jats:p><\/jats:sec><jats:sec><jats:title>Interpretation<\/jats:title><jats:p>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\u2013risk ratio of this therapy.<\/jats:p><\/jats:sec>","DOI":"10.1002\/acn3.51772","type":"journal-article","created":{"date-parts":[[2023,5,11]],"date-time":"2023-05-11T08:02:28Z","timestamp":1683792148000},"page":"904-917","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":10,"title":["Focal lesions following intracerebral gene therapy for mucopolysaccharidosis <scp>IIIA<\/scp>"],"prefix":"10.1002","volume":"10","author":[{"given":"Marianna","family":"Bugiani","sequence":"first","affiliation":[{"name":"Department of Pathology Amsterdam University Medical Centers, Vrije Universiteit and Amsterdam Neuroscience  Amsterdam The Netherlands"},{"name":"Amsterdam Leukodystrophy Center Amsterdam University Medical Centers  Amsterdam The Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6932-0449","authenticated-orcid":false,"given":"Truus E. 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