Evidence map›Paper›PMID 28729303›Full record

ArticleHaematologica2017

Amotosalen/ultraviolet A pathogen inactivation technology reduces platelet activatability, induces apoptosis and accelerates clearance.

Simona Stivala, Sara Gobbato, Laura Infanti, Martin F Reiner, Nicole Bonetti, Sara C Meyer, Giovanni G Camici, Thomas F Lüscher, Andreas Buser, Jürg H Beer

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 57 citations in OpenAlex.

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  5. Increase of Phosphoprotein Expressions in Amotosalen/UVA-Treated Platelet Concentrates.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 1 country.

Simona StivalaLaboratory for Platelet Research, Center for Molecular Cardiology, University of Zurich, Switzerland.
Sara GobbatoLaboratory for Platelet Research, Center for Molecular Cardiology, University of Zurich, Switzerland.
Laura InfantiRegional Blood Transfusion Service of the Swiss Red Cross, Basel, Switzerland.
Martin F ReinerLaboratory for Platelet Research, Center for Molecular Cardiology, University of Zurich, Switzerland.
Nicole BonettiLaboratory for Platelet Research, Center for Molecular Cardiology, University of Zurich, Switzerland.
Sara C MeyerDivision of Hematology and Department of Biomedicine, University Hospital Basel, Switzerland.
Giovanni G CamiciCenter of Molecular Cardiology, University of Zurich, Switzerland.
Thomas F LüscherDepartment of Cardiology, University Heart Center, University Hospital Zurich, Switzerland.
Andreas BuserRegional Blood Transfusion Service of the Swiss Red Cross, Basel, Switzerland.
Jürg H BeerLaboratory for Platelet Research, Center for Molecular Cardiology, University of Zurich, Switzerland hansjuerg.beer@ksb.ch.
Kantonsspital Baden · CHSwiss Red Cross · CHUniversity Hospital of Basel · CHUniversity Hospital of Zurich · CHUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amotosalen and ultraviolet A (UVA) photochemical-based pathogen reduction using the Intercept™ Blood System (IBS) is an effective and established technology for platelet and plasma components, which is adopted in more than 40 countries worldwide. Several reports point towards a reduced platelet function after Amotosalen/UVA exposure. The study herein was undertaken to identify the mechanisms responsible for the early impairment of platelet function by the IBS. Twenty-five platelet apheresis units were collected from healthy volunteers following standard procedures and split into 2 components, 1 untreated and the other treated with Amotosalen/UVA. Platelet impedance aggregation in response to collagen and thrombin was reduced by 80% and 60%, respectively, in IBS-treated units at day 1 of storage. Glycoprotein Ib (GpIb) levels were significantly lower in IBS samples and soluble glycocalicin correspondingly augmented; furthermore, GpIbα was significantly more desialylated as shown by

Indexed as

Ultraviolet RaysAnimalsApoptosisbcl-2 Homologous Antagonist-Killer ProteinBlood PlateletsCell SurvivalCollagenFurocoumarinsHumansMiceMice, Inbred NODMice, SCIDp38 Mitogen-Activated Protein KinasesPlatelet ActivationPlatelet AdhesivenessPlatelet Aggregationadhesion receptoramotosalenbcl-2 Homologous Antagonist-Killer ProteinCollagenFurocoumarinsglycocalicinp38 Mitogen-Activated Protein KinasesPlatelet Glycoprotein GPIb-IX Complexvon Willebrand Factor

Identifiers

PMID28729303
PMCPMC5622849
OpenAlexW2738233098

What OpenQuestion holds

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LicenceCC BY-NC
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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.