Evidence map›Paper›PMID 39342429›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2024

Anti-amyloid treatment is broadly effective in neuronopathic mucopolysaccharidoses and synergizes with gene therapy in MPS-IIIA.

Marianna Giaccio, Antonio Monaco, Laura Galiano, Andrea Parente, Luigi Borzacchiello, Riccardo Rubino, Frank-Gerrit Klärner, Dennis Killa, Claudia Perna, Pasquale Piccolo and 9 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Advances in Therapies for Mucopolysaccharidoses.Current issues in molecular biology · 2026
    Review
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Marianna GiaccioCEINGE-Biotecnologie Avanzate Franco Salvatore, Via G. Salvatore, 486 Napoli, Italy.
Antonio MonacoCEINGE-Biotecnologie Avanzate Franco Salvatore, Via G. Salvatore, 486 Napoli, Italy.
Laura GalianoCEINGE-Biotecnologie Avanzate Franco Salvatore, Via G. Salvatore, 486 Napoli, Italy.
Andrea ParenteCEINGE-Biotecnologie Avanzate Franco Salvatore, Via G. Salvatore, 486 Napoli, Italy; Dipartimento di Scienze Mediche Traslazionali, Università Degli Studi di Napoli "Federico II" Via S. Pansini, 5, Napoli, Italy.
Luigi BorzacchielloCEINGE-Biotecnologie Avanzate Franco Salvatore, Via G. Salvatore, 486 Napoli, Italy; Dipartimento di Scienze Mediche Traslazionali, Università Degli Studi di Napoli "Federico II" Via S. Pansini, 5, Napoli, Italy.
Riccardo RubinoCEINGE-Biotecnologie Avanzate Franco Salvatore, Via G. Salvatore, 486 Napoli, Italy.
Frank-Gerrit KlärnerDepartment of Chemistry, University of Duisburg-Essen, Universitaetsstrasse 7, 45117 Essen, Germany.
Dennis KillaDepartment of Chemistry, University of Duisburg-Essen, Universitaetsstrasse 7, 45117 Essen, Germany.
Claudia PernaTelethon Institute of Genetics and Medicine (TIGEM), Via C. Flegrei, 34, Pozzuoli, Napoli, Italy.
Pasquale PiccoloTelethon Institute of Genetics and Medicine (TIGEM), Via C. Flegrei, 34, Pozzuoli, Napoli, Italy.
Marcello MarottaDipartimento di Medicina Clinica e Chirurgia, Università Degli Studi di Napoli "Federico II" Via S. Pansini, 5, Napoli, Italy.
Xuefang PanDepartment of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Center, University of Montreal, Montreal, QC, Canada.
Marie KhijniakDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
Ibrar SiddiqueDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA.
Thomas SchraderDepartment of Chemistry, University of Duisburg-Essen, Universitaetsstrasse 7, 45117 Essen, Germany.
Alexey V PshezhetskyDepartment of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine Research Center, University of Montreal, Montreal, QC, Canada.
Nicolina Cristina SorrentinoTelethon Institute of Genetics and Medicine (TIGEM), Via C. Flegrei, 34, Pozzuoli, Napoli, Italy; Dipartimento di Medicina Clinica e Chirurgia, Università Degli Studi di Napoli "Federico II" Via S. Pansini, 5, Napoli, Italy.
Gal BitanDepartment of Neurology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, USA; Brain Research Institute and Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA, USA.
Alessandro FraldiCEINGE-Biotecnologie Avanzate Franco Salvatore, Via G. Salvatore, 486 Napoli, Italy; Dipartimento di Medicina Clinica e Chirurgia, Università Degli Studi di Napoli "Federico II" Via S. Pansini, 5, Napoli, Italy. Electronic address: alessandro.fraldi@unina.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mucopolysaccharidoses (MPSs) are childhood diseases caused by inherited deficiencies in glycosaminoglycan degradation. Most MPSs involve neurodegeneration, which to date is untreatable. Currently, most therapeutic strategies aim at correcting the primary genetic defect. Among these strategies, gene therapy has shown great potential, although its clinical application is challenging. We have shown previously in an MPS-IIIA mouse model that the molecular tweezer (MT) CLR01, a potent, broad-spectrum anti-amyloid small molecule, inhibits secondary amyloid storage, facilitates amyloid clearance, and protects against neurodegeneration. Here, we demonstrate that combining CLR01 with adeno-associated virus (AAV)-mediated gene therapy, targeting both the primary and secondary pathologic storage in MPS-IIIA mice, results in a synergistic effect that improves multiple therapeutic outcomes compared to each monotherapy. Moreover, we demonstrate that CLR01 is effective therapeutically in mouse models of other forms of neuronopathic MPS, MPS-I, and MPS-IIIC. These strongly support developing MTs as an effective treatment option for neuronopathic MPSs, both on their own and in combination with gene therapy, to improve therapeutic efficacy and translation into clinical application.

Indexed as

DependovirusDisease Models, AnimalGenetic TherapyGenetic VectorsAmyloidAnimalsBiological ProductsCombined Modality TherapyHumansMiceMucopolysaccharidosesMucopolysaccharidosis IIIRecombinant Fusion ProteinsAmyloidBiological ProductsRecombinant Fusion ProteinsZolgensmaAAV gene therapyamyloid proteinscombined therapylysosomal storage disordersmolecular tweezersmucopolysaccharidosesneuronopathy

Identifiers

PMID39342429
PMCPMC11573617

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.