Evidence map›Paper›PMID 28874674›Full record

Trial reportScientific reports2017

Lytic EBV infection investigated by detection of Soluble Epstein-Barr virus ZEBRA in the serum of patients with PTLD.

Mohammed Habib, Marlyse Buisson, Julien Lupo, Felix Agbalika, Gérard Socié, Raphaele Germi, Monique Baccard, Berthe-Marie Imbert-Marcille, Jacques Dantal, Patrice Morand and 1 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Biomarkers for PTLD diagnosis and therapies.Pediatric nephrology (Berlin, Germany) · 2020
    Review
  12. Review
  13. 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

11 authors at 3 institutions in 1 country.

Mohammed HabibInstitut de Biologie Structurale (IBS), Université Grenoble Alpes, CEA, CNRS, Grenoble, France.
Marlyse BuissonInstitut de Biologie Structurale (IBS), Université Grenoble Alpes, CEA, CNRS, Grenoble, France.
Julien LupoUnit of Virology, University, Hospital, Université Grenoble Alpes, Grenoble, France.
Felix AgbalikaUnit of Virology, Hôpital Saint-Louis, AP-HP, Université Paris-Diderot, Paris, France.
Gérard SociéUnit of Clinical Hematology, Hôpital Saint-Louis, AP-HP, Université Paris-Diderot, Paris, France.
Raphaele GermiUnit of Virology, University, Hospital, Université Grenoble Alpes, Grenoble, France.
Monique BaccardUnit of Virology, University, Hospital, Université Grenoble Alpes, Grenoble, France.
Berthe-Marie Imbert-MarcilleUnit of Virology, University Hospital, Université de Nantes, Nantes, France.
Jacques DantalUnit of Nephrology & Clinical Immunology, University Hospital, Université de Nantes, Nantes, France.
Patrice MorandUnit of Virology, University, Hospital, Université Grenoble Alpes, Grenoble, France.
Emmanuel DrouetInstitut de Biologie Structurale (IBS), Université Grenoble Alpes, CEA, CNRS, Grenoble, France. emmanuel.drouet@ibs.fr.
Université Grenoble Alpes · FRNantes Université · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ZEBRA protein (encoded by the BZLF1 gene), is the major transcription factor of EBV, expressed upon EBV lytic cycle activation. Several studies highlighted the critical role of EBV lytic infection as a risk factor for lymphoproliferative disorders like post-transplant lymphoproliferative disease (PTLD). Here, we use an antigen-capture ELISA assay specifically designed to detecting the circulating soluble ZEBRA (sZEBRA) in serum samples (threshold value determined at 40ng/mL). We retrospectively investigated a population of 66 transplanted patients comprising 35 PTLD. All the samples from a control population (30 EBV-seronegative subjects and 25 immunocompetent individuals with EBV serological reactivation), classified as sZEBRA < 40ng/mL were assigned as negative. At PTLD diagnosis, EBV genome (quantified by qPCR with EBV DNA>200 copies/mL) and sZEBRA were detectable in 51% and 60% of cases, respectively. In the patients who developed a pathologically-confirmed PTLD, the mean sZEBRA value in cases, was 399 ng/mL +/- 141 versus 53ng/mL +/- 7 in patients who did not (p  < 0,001). This is the first report relating to the detection of the circulating ZEBRA in serum specimens, as well as the first analysis dealing with the lytic cycle of EBV in PTLD patients with this new biomarker.

Indexed as

AdolescentAdultAgedChildEnzyme-Linked Immunosorbent AssayEpstein-Barr Virus InfectionsFemaleHumansKidney TransplantationLung TransplantationLymphoproliferative DisordersMaleMiddle AgedSerologic TestsTrans-ActivatorsBZLF1 protein, Herpesvirus 4, HumanTrans-Activators

Identifiers

PMID28874674
PMCPMC5585268
OpenAlexW2752773376

What OpenQuestion holds

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LicenceCC BY
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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.