Focal lesions following intracerebral gene therapy for mucopolysaccharidosis IIIA

被引:8
作者
Bugiani, Marianna [1 ,2 ,3 ]
Abbink, Truus E. M. [3 ,4 ]
Edridge, Arthur W. D. [2 ,5 ,6 ]
van der Hoek, Lia [2 ]
Hillen, Anne E. J. [3 ,4 ]
van Til, Niek P. [3 ,4 ]
Hu-A-Ng, Gino V. [3 ,4 ]
Breur, Marjolein [3 ,4 ]
Aiach, Karen [7 ]
Drevot, Philippe [7 ]
Hocquemiller, Michael [7 ]
Laufer, Ralph [7 ]
Wijburg, Frits A. [8 ,9 ]
van der Knaap, Marjo S. [3 ,4 ,10 ,11 ]
机构
[1] Vrije Univ, Amsterdam Univ, Dept Pathol, Med Ctr, Amsterdam, Netherlands
[2] Amsterdam Neurosci, Amsterdam, Netherlands
[3] Univ Amsterdam, Amsterdam Leukodystrophy Ctr, Med Ctr, Amsterdam, Netherlands
[4] Vrije Univ, Amsterdam Univ, Emma Childrens Hosp, Med Ctr,Dept Child Neurol, Amsterdam, Netherlands
[5] Univ Amsterdam, Amsterdam Univ, Dept Med Microbiol & Infect Prevent, Med Ctr,Lab Expt Virol, Amsterdam, Netherlands
[6] Univ Amsterdam, Amsterdam Ctr Global Child Hlth, Med Ctr, Amsterdam, Netherlands
[7] Lysogene, Neuilly Sur Seine, France
[8] Emma Childrens Hosp, Dept Pediat Metab Dis, Amsterdam, Netherlands
[9] Univ Amsterdam, Acad Med Ctr, Amsterdam Lysosome Ctr Sphinx, Med Ctr, Amsterdam, Netherlands
[10] Vrije Univ Amsterdam, Ctr Neurogenom & Cognit Res, Dept Integrat Neurophysiol, NL-1081 HV Amsterdam, Netherlands
[11] Univ Amsterdam, Emma Childrens Hosp, Locat VU Med Ctr, Med Ctr,Dept Child Neurol, Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
关键词
VANISHING WHITE-MATTER; SANFILIPPO-SYNDROME; NATURAL-HISTORY; DISEASE; MATURATION; PATHOLOGY; GLYCOSAMINOGLYCAN; DIAGNOSIS; SGSH;
D O I
10.1002/acn3.51772
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:904 / 917
页数:14
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