Evidence map›Paper›PMID 41022755›Full record

ArticleNature communications2025

Development of an adeno-associated virus vector for gene replacement therapy of NF1-related tumors.

Ren-Yuan Bai, Jingyi Shi, Jianan Liu, Nihao Sun, Yuqing Lu, Xiaojun Chen, Manzhu Xu, Hotae Lim, Yang Li, Huazhen Xu and 8 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

18 authors.

Ren-Yuan BaiKennedy Krieger Institute, Baltimore, MD, USA. rbai1@jhmi.edu.ORCID http://orcid.org/0000-0001-5281-9091
Jingyi ShiKennedy Krieger Institute, Baltimore, MD, USA.
Jianan LiuKennedy Krieger Institute, Baltimore, MD, USA.
Nihao SunKennedy Krieger Institute, Baltimore, MD, USA.
Yuqing LuKennedy Krieger Institute, Baltimore, MD, USA.
Xiaojun ChenKennedy Krieger Institute, Baltimore, MD, USA.ORCID http://orcid.org/0009-0007-9098-1680
Manzhu XuDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Hotae LimDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Yang LiKennedy Krieger Institute, Baltimore, MD, USA.
Huazhen XuKennedy Krieger Institute, Baltimore, MD, USA.
Karis WeisgerberKennedy Krieger Institute, Baltimore, MD, USA.
Zhihong RenDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Christine A PratilasDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID http://orcid.org/0000-0002-7116-0605
Jaishri O BlakeleyDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID http://orcid.org/0000-0002-1049-0993
Melissa L FishelDepartment of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, USA.ORCID http://orcid.org/0000-0002-9436-6382
Meritxell CarrióHereditary Cancer Group, Germans Trias i Pujol Research Institute (IGTP), CARE Program, Badalona, Barcelona, Spain.
Eduard SerraHereditary Cancer Group, Germans Trias i Pujol Research Institute (IGTP), CARE Program, Badalona, Barcelona, Spain.ORCID http://orcid.org/0000-0003-2895-9857
Verena StaedtkeKennedy Krieger Institute, Baltimore, MD, USA.

Funding

Sontag Foundation Distinguished Scientist AwardUnited States Department of Defense | United States Army | Army Medical Command | Congressionally Directed Medical Research Programs (CDMRP) W81XWH1810236U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) 1K08CA230179U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) 5U01CA247576
6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is a tumor predisposition syndrome caused by alterations in NF1 gene that lead to tumor growth throughout the nervous system, which can cause morbidity and mortality, and transform to malignancy. NF1 gene replacement therapy, though promising, is hindered by NF1 gene's large size and delivery challenges. We introduced a membrane-targeted, truncated neurofibromin comprising the GAP-related domain (GRD) fused to the KRAS4B C-terminal domain, which effectively inhibits the RAS signaling pathway and restores Schwann cell differentiation in an NF1 iPSC-derived model. For systemic application, we engineered an adeno-associated virus (AAV) vector using in vivo capsid evolution through sequential DNA shuffling and peptide library screening in a NF1 xenograft mouse model. This tailored vector, AAV-NF, exhibits greatly reduced liver uptake, enhanced tumor targeting across various NF1-related MPNST, neurofibromas and glioma models, and therapeutic efficacy in xenografts of MPNST. This study not only advances a viable AAV vector for NF1 treatment but also outlines a replicable strategy for vector and payload development in other monogenic and tumor-associated disease manifestations.

Indexed as

DependovirusGenetic TherapyGenetic VectorsNeurofibromatosis 1Neurofibromin 1AnimalsFemaleHumansInduced Pluripotent Stem CellsMiceProto-Oncogene Proteins p21(ras)Schwann CellsXenograft Model Antitumor AssaysNeurofibromin 1NF1 protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID41022755
PMCPMC12480499

What OpenQuestion holds

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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.