Evidence map›Paper›PMID 30962537›Full record

ArticleGene therapy2019

Adeno-associated virus neutralising antibodies in type 1 diabetes mellitus.

Slawomir Andrzejewski, Aparna Murali, Charmaine Ramlogan-Steel, Katie P Edwards, Nathan Efron, Jason C Steel, Christopher J Layton

Abstract read
PubMed Publisher
In one paragraph

Article in Gene therapy, 2019. 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
0.5field-weighted citation impact, top 28% 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.

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, 3 citations in OpenAlex.

  1. Gene Therapy Strategies for Uveal Melanoma: Adeno-associated Virus Delivery Challenges and Translational Opportunities.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  2. Article
  3. Article
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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

7 authors at 2 institutions in 1 country.

Slawomir AndrzejewskiLVF Ophthalmology Research Centre, Translational Research Institute, 37 Kent St, Woolloongabba, Brisbane, QLD, 4102, Australia.
Aparna MuraliLVF Ophthalmology Research Centre, Translational Research Institute, 37 Kent St, Woolloongabba, Brisbane, QLD, 4102, Australia.
Charmaine Ramlogan-SteelLVF Ophthalmology Research Centre, Translational Research Institute, 37 Kent St, Woolloongabba, Brisbane, QLD, 4102, Australia.
Katie P EdwardsInstitute of Health and Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Kelvin Grove, Brisbane, QLD, 4059, Australia.
Nathan EfronInstitute of Health and Biomedical Innovation, Queensland University of Technology, 60 Musk Avenue, Kelvin Grove, Brisbane, QLD, 4059, Australia.
Jason C SteelLVF Ophthalmology Research Centre, Translational Research Institute, 37 Kent St, Woolloongabba, Brisbane, QLD, 4102, Australia.
Christopher J LaytonLVF Ophthalmology Research Centre, Translational Research Institute, 37 Kent St, Woolloongabba, Brisbane, QLD, 4102, Australia. c.layton@uq.edu.au.ORCID http://orcid.org/0000-0001-6933-9991
Translational Research Institute · AUQueensland University of Technology · AU

Funding

Juvenile Diabetes Research Foundation Australia (JDRF Australia) JDRFI 8-2008-362
6 · The paper itself

Abstract

Recombinant Adeno-associated viruses (AAVs) are an attractive vector for gene therapy delivery which may be blocked by AAV neutralising antibodies (NAbs). As Type 1 Diabetes (T1DM) is an endocrine disease of immunological origin, it is likely that NAb profiles are altered in the disease. In this study NAb to AAV2, AAV5, AAV6, and AAV8 in 72 subjects with T1DM and 45 non-diabetic patients were measured over a 4-year follow-up period. AAV2 NAb titres were significantly lower in non-diabetic subjects (P = 0.036). The T1DM group had more AAV8 NAb activity at baseline (P = 0.019), whilst after 4 years follow-up the T1DM group displayed developed increased AAV 5 (P = 0.03), 6 (P = 0.03) and 8 (P = 0.002) activity relative to the control group, however, overall AAV5 and 8 NAb levels were very low in patients <40. AAV NAb titre activity and prevalence generally appears higher in T1DM, however, low levels of AAV 5 and 8, particular in younger adult age groups at which T1DM can be targeted, could make these attractive vectors to target the disease.

Indexed as

AdolescentAdultAgedAnimalsAntibodies, NeutralizingChlorocebus aethiopsCOS CellsDependovirusDiabetes Mellitus, Type 1FemaleGene Transfer TechniquesHumansMaleMiddle AgedAntibodies, Neutralizing

Identifiers

PMID30962537
OpenAlexW2933734725

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.