Evidence map›Paper›PMID 29064732›Full record

ArticleHuman gene therapy. Clinical development2017

Differential Prevalence of Antibodies Against Adeno-Associated Virus in Healthy Children and Patients with Mucopolysaccharidosis III: Perspective for AAV-Mediated Gene Therapy.

Haiyan Fu, Aaron S Meadows, Ricardo J Pineda, Krista L Kunkler, Kristen V Truxal, Kim L McBride, Kevin M Flanigan, Douglas M McCarty

3 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in Human gene therapy. Clinical development, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
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.

NCT02716246 phase2 / phase3recruitingnot on this map

Phase I/II/III Gene Transfer Clinical Trial of scAAV9.U1a.hSGSH for Mucopolysaccharidosis (MPS) IIIA

TypeinterventionalSponsorUltragenyx Pharmaceutical IncRan2016 to 2029Enrolled36ConditionsMPS IIIA, Sanfilippo Syndrome, Sanfilippo A, Mucopolysaccharidosis IIIArmsUX111, Prophylactic Immunomodulatory (IM) Therapy, Optimized Prophylactic IM Therapy, Adjuvant IM Therapy
NCT03955679 approved for marketingnot on this map

A Managed Access Program (MAP) Cohort Treatment Protocol to Provide AVXS-101 to Patients With a Genetic Diagnosis of Spinal Muscular Atrophy (SMA) With 1, 2 or 3 Copies of SMN2

Typeexpanded_accessSponsorUnited BioSource, LLCConditionsSpinal Muscular AtrophyArmsAVXS-101
NCT04088734 phase1 / phase2terminatednot on this mapstarted 2019, after this paper: background citation

A Phase I/II Open Label, Single-dose, Gene Transfer Study of scAAV9.U1a.hSGSH (ABO-102) in Patients With Middle and Advanced Phases of MPS IIIA Disease

TypeinterventionalSponsorUltragenyx Pharmaceutical IncRan2019 to 2022Enrolled5ConditionsMPS IIIA, Sanfilippo Syndrome, Sanfilippo A, Mucopolysaccharidosis IIIArmsABO-102
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Binding and neutralizing anti-AAV antibodies: Detection and implications for rAAV-mediated gene therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Review
  13. Article
  14. Article
  15. Review
  16. Delivering gene therapy for mucopolysaccharide diseases.Frontiers in molecular biosciences · 2022
    Review
  17. Review
  18. Gene Therapy for Neuronopathic Mucopolysaccharidoses: State of the Art.International journal of molecular sciences · 2021
    Review
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Haiyan Fu1 Center for Gene Therapy, Research Institute at Nationwide Children's Hospital , Columbus, Ohio.
Aaron S Meadows1 Center for Gene Therapy, Research Institute at Nationwide Children's Hospital , Columbus, Ohio.
Ricardo J Pineda1 Center for Gene Therapy, Research Institute at Nationwide Children's Hospital , Columbus, Ohio.
Krista L Kunkler1 Center for Gene Therapy, Research Institute at Nationwide Children's Hospital , Columbus, Ohio.
Kristen V Truxal1 Center for Gene Therapy, Research Institute at Nationwide Children's Hospital , Columbus, Ohio.
Kim L McBride2 Center for Cardiovascular Research, Research Institute at Nationwide Children's Hospital , Columbus, Ohio.
Kevin M Flanigan1 Center for Gene Therapy, Research Institute at Nationwide Children's Hospital , Columbus, Ohio.
Douglas M McCarty1 Center for Gene Therapy, Research Institute at Nationwide Children's Hospital , Columbus, Ohio.
Nationwide Children's Hospital · US

Funding

Treating the CNS and Somatic Diseases of MPS IIIB by Systemic Gene DeliveryU01NS069626 · NINDS · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI FLANIGAN, KEVIN M, FU, HAIYAN · 2011 to 2014
$4.3M
PATTERNS OF r AAV VECTOR INSERTION ASSOCIATED WITH LIVER TUMORS IN A MOUSE MODELR01CA172713 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FU, HAIYAN · 2013 to 2017
$1.5M
NCI NIH HHS R01 CA172713NINDS NIH HHS U01 NS069626
6 · The paper itself

Abstract

Recombinant adeno-associated virus (AAV) vectors are promising gene therapy tools. However, pre-existing antibodies (Abs) to many useful AAV serotypes pose a critical challenge for the translation of gene therapies. As part of AAV gene therapy program for treating mucopolysaccharidosis (MPS) III patients, the seroprevalence profiles of AAV1-9 and rh74 were investigated in MPS IIIA/IIIB patients and in healthy children. Using enzyme-linked immunosorbent assay for αAAV-IgG, significantly higher seroprevalence was observed for AAV1 and AAVrh74 in 2- to 7-year-old MPS III patients than in healthy controls. Seroprevalence for the majority of tested AAV serotypes appears to peak before 8 years of age in MPS III subjects, with the exception of increases in αAAV8 and αAAV9 Abs in 8- to 19-year-old MPS IIIA patients. In contrast, significant increases in seroprevalence were observed for virtually all tested AAV serotypes in 8- to 15-year-old healthy children compared to 2- to 7-year-olds. Co-prevalence and Ab level correlation results followed the previously established divergence-based clade positions of AAV1-9. Interestingly, the individuals positive for αAAVrh74-Abs showed the lowest co-prevalence with Abs for AAV1-9 (22-40%). However, all or nearly all (77-100%) of subjects who were seropositive for any of serotypes 1-9 were also positive for αAAVrh74-IgG. Notably, the majority (78%) of αAAV seropositive individuals were also Ab-positive for one to five of the tested AAV serotypes, mostly with low levels of αAAV-Abs (1:50-100), while a minority (22%) were seropositive for six or more AAV serotypes, mostly with high levels of αAAV-IgG for multiple serotypes. In general, the highest IgG levels were reactive to AAV2, AAV3, and AAVrh74. The data illustrate the complex seroprevalence profiles of AAV1-9 and rh74 in MPS patients and healthy children, indicating the potential association of AAV seroprevalence with age and disease conditions. The broad co-prevalence of Abs for different AAV serotypes reinforces the challenge of pre-existing αAAV-Abs for translating AAV gene therapy to clinical applications, regardless of the vector serotype.

Indexed as

Genetic TherapyAntibodies, ViralChildDependovirusEnzyme-Linked Immunosorbent AssayGenetic VectorsHumansMucopolysaccharidosis IIIPrevalenceSeroepidemiologic StudiesSerogroupAntibodies, ViralAAVMPS IIIpre-existing Absseroprevalance

Identifiers

PMID29064732
PMCPMC6435348
OpenAlexW2889246339

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.