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| Verfasst von: | Roubertie, Agathe [VerfasserIn]  |
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| | Opladen, Thomas [VerfasserIn] |
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| | Brennenstuhl, Heiko [VerfasserIn] |
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| | Kuseyri Hübschmann, Oya [VerfasserIn] |
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| | Flint, Lisa [VerfasserIn] |
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| | Willemsen, Michel A. [VerfasserIn] |
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| | Leuzzi, Vincenzo [VerfasserIn] |
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| | Cazorla, Angels Garcia [VerfasserIn] |
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| | Kurian, Manju A. [VerfasserIn] |
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| | François-Heude, Marie Céline [VerfasserIn] |
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| | Hwu, Paul [VerfasserIn] |
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| | Zeev, Bruria Ben [VerfasserIn] |
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| | Kiening, Karl [VerfasserIn] |
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| | Roujeau, Thomas [VerfasserIn] |
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| | Pons, Roser [VerfasserIn] |
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| | Pearson, Toni S. [VerfasserIn] |
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| Titel: | Gene therapy for aromatic L-amino acid decarboxylase deficiency |
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| Titelzusatz: | requirements for safe application and knowledge-generating follow-up |
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| Verf.angabe: | Agathe Roubertie, Thomas Opladen, Heiko Brennenstuhl, Oya Kuseyri Hübschmann, Lisa Flint, Michel A. Willemsen, Vincenzo Leuzzi, Angels Garcia Cazorla, Manju A. Kurian, Marie Céline François-Heude, Paul Hwu, Bruria Ben Zeev, Karl Kiening, Thomas Roujeau, Roser Pons, Toni S. Pearson |
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| E-Jahr: | 2023 |
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| Jahr: | 04 July 2023 |
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| Umfang: | 13 S. |
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| Fussnoten: | Gesehen am 09.08.2023 |
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| Titel Quelle: | Enthalten in: Journal of inherited metabolic disease |
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| Ort Quelle: | Hoboken, NJ : Wiley, 1978 |
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| Jahr Quelle: | 2023 |
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| Band/Heft Quelle: | (2023), Seite 1-13 |
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| ISSN Quelle: | 1573-2665 |
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| Abstract: | The autosomal recessive defect of aromatic L-amino acid decarboxylase (AADC) leads to a severe neurological disorder with manifestation in infancy due to a pronounced, combined deficiency of dopamine, serotonin and catecholamines. The success of conventional drug treatment is very limited, especially in patients with a severe phenotype. The development of an intracerebral AAV2-based gene delivery targeting the putamen or substantia nigra started more than 10 years ago. Recently, the putaminally-delivered construct, Eladocagene exuparvovec has been approved by the European Medicines Agency and by the British Medicines and Healthcare products Regulatory Agency. This now available gene therapy provides for the first time also for AADC deficiency (AADCD) a causal therapy, leading this disorder into a new therapeutic era. By using a standardized Delphi approach members of the International Working Group on Neurotransmitter related Disorders (iNTD) developed structural requirements and recommendations for the preparation, management and follow-up of AADC deficiency patients who undergo gene therapy. This statement underlines the necessity of a framework for a quality-assured application of AADCD gene therapy including Eladocagene exuparvovec. Treatment requires prehospital, inpatient and posthospital care by a multidisciplinary team in a specialized and qualified therapy center. Due to lack of data on long-term outcomes and the comparative efficacy of alternative stereotactic procedures and brain target sites, a structured follow-up plan and systematic documentation of outcomes in a suitable, industry-independent registry study are necessary. |
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| DOI: | doi:10.1002/jimd.12649 |
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| URL: | kostenfrei: Volltext: https://doi.org/10.1002/jimd.12649 |
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| | kostenfrei: Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/jimd.12649 |
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| | DOI: https://doi.org/10.1002/jimd.12649 |
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| Datenträger: | Online-Ressource |
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| Sprache: | eng |
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| Sach-SW: | AADCD |
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| | Aromatic L-amino acid decarboxylase |
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| | Eladocagene exuparvovec |
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| | gene therapy |
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| | iNTD registry |
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| | neurotransmitter |
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| K10plus-PPN: | 1855006219 |
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| Verknüpfungen: | → Zeitschrift |
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| Lokale URL UB: |  Zum Volltext |
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Gene therapy for aromatic L-amino acid decarboxylase deficiency / Roubertie, Agathe [VerfasserIn]; 04 July 2023 (Online-Ressource)
