Evidence map›Paper›PMID 40140720›Full record

ArticleGene therapy2025

Optimization of adeno-associated viral (AAV) gene therapies vectors for balancing efficacy, longevity and safety for clinical application.

Neel Mehta, Rénald Gilbert, Parminder S Chahal, Maria J Moreno, Nasha Nassoury, Nathalie Coulombe, Richard Gingras, Alaka Mullick, Simon Drouin, Marc Sasseville and 7 more

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. [Adeno-associated virus-mediated gene therapy for genetic epilepsy: prospects and challenges].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2026
    Review
  5. Article
  6. Review
  7. 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

17 authors.

Neel MehtaCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Rénald GilbertBioprocess Engineering Department, Human Health Therapeutics Research Centre, National Research Council Canada, Montréal, QC, Canada.ORCID 0000-0002-8265-2111
Parminder S ChahalBioprocess Engineering Department, Human Health Therapeutics Research Centre, National Research Council Canada, Montréal, QC, Canada.
Maria J MorenoDigital Health and Molecular Technologies, National Research Council Canada, Ottawa, ON, Canada.
Nasha NassouryBioprocess Engineering Department, Human Health Therapeutics Research Centre, National Research Council Canada, Montréal, QC, Canada.
Nathalie CoulombeBioprocess Engineering Department, Human Health Therapeutics Research Centre, National Research Council Canada, Montréal, QC, Canada.
Richard GingrasBioprocess Engineering Department, Human Health Therapeutics Research Centre, National Research Council Canada, Montréal, QC, Canada.
Alaka MullickBioprocess Engineering Department, Human Health Therapeutics Research Centre, National Research Council Canada, Montréal, QC, Canada.
Simon DrouinDigital Health and Molecular Technologies, National Research Council Canada, Ottawa, ON, Canada.
Marc SassevilleDigital Health and Molecular Technologies, National Research Council Canada, Ottawa, ON, Canada.
Jyoti LatawaBioprocess Engineering Department, Human Health Therapeutics Research Centre, National Research Council Canada, Montréal, QC, Canada.
Krishnaraj TiwariBioprocess Engineering Department, Human Health Therapeutics Research Centre, National Research Council Canada, Montréal, QC, Canada.
Wendy LinCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Emily M HarveyCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-8848-5529
Fudan MiaoCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Colin J D RossCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Michael R HaydenCentre for Molecular Medicine and Therapeutics, BC Children's Hospital Research Institute, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada. mrh@cmmt.ubc.ca.ORCID 0000-0001-5159-1419

Funding

Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) 201910MFE-430323-FPP-CAAA-267763Gouvernement du Canada | National Research Council Canada (Conseil national de recherches Canada) CGT-101Michael Smith Foundation for Health Research (MSFHR) RT-2020-0381
6 · The paper itself

Abstract

Adeno-associated viral (AAV) vectors are an ideal platform for gene therapy due to their ability to deliver therapeutic cargos safely and effectively across various target organs. Their low immunogenicity contributes to long-lasting therapeutic effects. However, recent insights highlight the significance of CpG content within AAV vectors, where unmethylated CpG dinucleotides can trigger a TLR9-mediated immune response, leading to the rapid elimination of transduced cells. Clinical evidence indicates an inverse relationship between CpG content and therapeutic success, with lower CpG counts correlating with sustained transgene expression. Here, we sought to optimize a novel, CpG-rich AAV8 vector, referred to as pVR59, designed for treating lipoprotein lipase deficiency (LPLD). We strategically reduced CpG levels in pVR59, resulting in the development of pNC182, a CpG-depleted vector that maintains therapeutic efficacy. A single intramuscular injection of pNC182 demonstrated comparable effectiveness to pVR59 in normalizing lipemia and hypertriglyceridemia in LPLD mouse models, with a 38% reduction in total CpG count. These findings support the clinical application of pNC182 as a safe, long-lasting AAV gene therapy for LPLD and provide a framework for future AAV vector designs aimed at maximizing therapeutic efficacy while minimizing immunogenic responses in human settings.

Indexed as

DependovirusGenetic TherapyGenetic VectorsHyperlipoproteinemia Type IAnimalsCpG IslandsDisease Models, AnimalHumansLipoprotein LipaseMiceLipoprotein Lipase

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.