Evidence map›Paper›PMID 35654086›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia2022

Plasma-derived FVIII/VWF complex shows higher protection against inhibitors than isolated FVIII after infusion in haemophilic patients: A translational study.

Maria Isabel Bravo, Alba Pérez, Aida Raventós, Salvador Grancha, Juan Ignacio Jorquera, Nora Viviana Butta, Maria Teresa Álvarez-Román, Montserrat Costa, Todd Willis, Victor Jiménez-Yuste

Open access · bronzeAbstract read
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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 3 institutions in 2 countries.

Maria Isabel BravoBioscience Research Group, Grifols, Barcelona, Spain.
Alba PérezBioscience Research Group, Grifols, Barcelona, Spain.
Aida RaventósBioscience Research Group, Grifols, Barcelona, Spain.
Salvador GranchaBioscience Research Group, Grifols, Barcelona, Spain.
Juan Ignacio JorqueraBioscience Research Group, Grifols, Barcelona, Spain.
Nora Viviana ButtaThrombosis and Haemostasis Unit - IdiPAZ, University Hospital La Paz, Madrid, Spain.ORCID https://orcid.org/0000-0003-4601-7150
Maria Teresa Álvarez-RománThrombosis and Haemostasis Unit - IdiPAZ, University Hospital La Paz, Madrid, Spain.ORCID https://orcid.org/0000-0003-3296-4288
Montserrat CostaBioscience Research Group, Grifols, Barcelona, Spain.
Todd WillisBioscience Research Group, Grifols, Raleigh, North Carolina, USA.
Victor Jiménez-YusteThrombosis and Haemostasis Unit - IdiPAZ, University Hospital La Paz, Madrid, Spain.ORCID https://orcid.org/0000-0003-3937-3499
Grifols (Spain) · ESHospital Universitario La Paz · ESBioscience Research · US

Funding

Grifols
6 · The paper itself

Abstract

introductionPresence of von Willebrand factor (VWF) in FVIII concentrates offers protection against neutralizing inhibitors in haemophilia A (HA). Whether this protection is more evident in plasma-derived (pd) FVIII/VWF or recombinant (r) FVIII concentrates remains controversial.

aimWe investigated the protection exerted by VWF against FVIII inhibitors in an in vivo mouse model of HA exposed to pdFVIII/VWF or to various rFVIII concentrates.

methodsHaemophilia A mice received the different FVIII concentrates after administration of vehicle or an inhibitory IgG purified from a commercial pool of HA plasma with inhibitors and FVIII:C recoveries were measured. Furthermore, using a novel clinically oriented ex vivo approach, Bethesda inhibitory activities (BU) of a commercial pool of HA plasma with inhibitors were assessed using normal plasma, or plasma from severe HA patients, without inhibitors, after treatment with the same concentrates.

resultsin vivo studies showed that pdFVIII/VWF offers markedly higher protection against inhibitors when compared with any of the FVIII products without VWF. More importantly, in the ex vivo studies, plasma from patients treated with pdFVIII/VWF showed higher protection against inhibitors (P values ranging .05-.001) in comparison with that observed in plasma from patients who received FVIII products without VWF, regardless of the type of product evaluated.

conclusionData indicate that FVIII+VWF complexes assembled in the circulation after rFVIII infusion are not equivalent to the naturally formed complex in pdFVIII/VWF. Therefore, rFVIII infused into HA patients with inhibitors would be less protected by VWF than the FVIII in pdFVIII/VWF concentrates.

Indexed as

Factor VIIIHemophilia Avon Willebrand FactorAnimalsDisease Models, AnimalImmunoglobulin GMiceRecombinant ProteinsFactor VIIIImmunoglobulin GRecombinant Proteinsvon Willebrand FactorFVIII inhibitorsFVIIInull E16 Knockout micehaemophilia A patientshaemophilia A treatmentplasma-derived FVIIIrecombinant FVIIIvon Willebrand factor

Identifiers

PMID35654086
PMCPMC9545517
OpenAlexW4281852214

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.