Evidence map›Paper›PMID 35677030›Full record

ArticleResearch and practice in thrombosis and haemostasis2022

Seroprevalence to adeno-associated virus type 6 in people with hemophilia B from a UK adult cohort.

Sara Boyce, Izabela James, Savita Rangarajan, Nicola Curry, Catherine Bagot, Steven Austin, Mike Laffan, Sarah Mangles, Kandiah Chandrakumaran, Carina Mundy

Open access · goldAbstract read
In one paragraph

Article in Research and practice in thrombosis and haemostasis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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
  5. Article
  6. 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

10 authors at 7 institutions in 1 country.

Sara BoyceSouthampton Haemophilia Comprehensive Care Centre University Hospital Southampton NHS Foundation Trust Southampton UK.ORCID https://orcid.org/0000-0002-0671-3269
Izabela JamesSouthampton Haemophilia Comprehensive Care Centre University Hospital Southampton NHS Foundation Trust Southampton UK.
Savita RangarajanUniversity of Southampton Southampton UK.
Nicola CurryOxford Haemophilia and Thrombosis Centre Oxford University Hospitals NHS Foundation Trust Oxford UK.
Catherine BagotWest of Scotland Haemophilia Centre Glasgow Royal Infirmary Glasgow UK.ORCID https://orcid.org/0000-0002-6439-9706
Steven AustinSt Georges Haemophilia Comprehensive Care Centre St George's University Hospitals NHS Foundation Trust London UK.
Mike LaffanCentre for Haematology Imperial College London UK.
Sarah ManglesHemophilia, Haemostasis and Thrombosis Centre Hampshire Hospitals NHS Foundation Trust Basingstoke UK.
Kandiah ChandrakumaranPeritoneal Malignancy Institute and Surgery Hampshire Hospitals NHS Foundation Trust Basingstoke UK.
Carina MundyUniversity of Southampton Southampton UK.
Hampshire Hospitals NHS Foundation Trust · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Southampton · GBGlasgow Royal Infirmary · GBImperial College London · GBOxford University Hospitals NHS Trust · GBSt George’s University Hospitals NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gene therapy shows promise as a potential "cure" for hemophilia A and B. Adeno-associated virus (AAV) vectors are the leading platform to deliver modified genetic code of factor VIII or IX to the liver effecting endogenous production. Patient exposure to wild-type AAV leads to the formation of neutralizing factors, which can prevent successful transduction. It is thus important to establish the seroprevalence of the AAV serotypes in people with hemophilia to aid prediction of successful gene transfer. The seroprevalence of AAV6 in UK people with hemophilia B is not yet reported. Objectives: We studied the prevalence of anti-AAV6 neutralizing factors in UK people with hemophilia B ( Methods: Serum samples and patient data were collected from 49 people with hemophilia B registered at UK hemophilia comprehensive care centers. The samples were tested for neutralizing factors to AAV6 using a cell-based transduction inhibition assay. Results: Thirty-one percent of patients had serum neutralization against AAV6. There was no correlation between AAV6 seropositivity and previous treatment with plasma-derived FIX products or hepatitis C exposure. Conclusion: Based on limited data, there is no evidence of association between the presence of AAV6 neutralizing factors in people with hemophilia B and exposure to contaminated plasma derivatives. The frequency of AAV6 neutralizing factors in our hemophilia B cohort is similar to UK people with hemophilia A and non-hemophilia populations.

Indexed as

AAVAAV6adeno‐associated virusgene therapyhemophilia Bseroprevalence

Identifiers

PMID35677030
PMCPMC9166283
OpenAlexW4281873183

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.