Evidence map›Paper›PMID 30036376›Full record

ArticlePloS one2018

Impact of IFN lambda 3/4 single nucleotide polymorphisms on the cytomegalovirus reactivation in autologous stem cell transplant patients.

Ombretta Annibali, Livia Piccioni, Valeria Tomarchio, Erika Circhetta, Chiara Sarlo, Luca Franceschini, Maria Cantonetti, Emanuela Rizzo, Silvia Angeletti, Maria Cristina Tirindelli and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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

14 authors at 3 institutions in 1 country.

Ombretta AnnibaliUnit of Hematology, Stem Cell Transplantation, Campus Bio-Medico University, Rome, Italy.
Livia PiccioniLaboratory of Virology, Campus Bio-Medico University, Rome, Italy.
Valeria TomarchioUnit of Hematology, Stem Cell Transplantation, Campus Bio-Medico University, Rome, Italy.
Erika CirchettaUnit of Hematology, Stem Cell Transplantation, Campus Bio-Medico University, Rome, Italy.
Chiara SarloUnit of Hematology, Stem Cell Transplantation, Campus Bio-Medico University, Rome, Italy.
Luca FranceschiniHematology and Stem Cell Transplant Unit, Tor Vergata University, Rome, Italy.
Maria CantonettiHematology and Stem Cell Transplant Unit, Tor Vergata University, Rome, Italy.
Emanuela RizzoHematology and Stem Cell Transplant Unit, Tor Vergata University, Rome, Italy.
Silvia AngelettiLaboratory of Pathology and Microbiology, Campus Bio-Medico University, Rome, Italy.
Maria Cristina TirindelliTransfusion Medicine and Cellular Therapy, Campus Bio-Medico University, Rome, Italy.
Carolina ScagnolariDepartment of Molecular Medicine, Laboratory of Virology, "Sapienza" University, Rome, Italy.
Maura StatzuDepartment of Molecular Medicine, Laboratory of Virology, "Sapienza" University, Rome, Italy.
Giuseppe AvvisatiUnit of Hematology, Stem Cell Transplantation, Campus Bio-Medico University, Rome, Italy.
Elisabetta RivaLaboratory of Virology, Campus Bio-Medico University, Rome, Italy.ORCID 0000-0002-6870-8780
Università Campus Bio-Medico · ITUniversity of Rome Tor Vergata · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytomegalovirus (CMV) infection represents one of the main cause mortality after Stem Cell Transplantation. Recently, a protective effect of the T allele of rs12979860 IL28B Single Nucleotide Polymorphisms (SNPs) against CMV infection in the allogenic stem cell transplantation was suggested. We investigate whether the rs12979860 IL28B SNP and the relative rs368234815 (IFNλ4) genotype may affect the incidence of active CMV infection in Autologous stem cell transplantation (Auto-SCT) setting. The study included 99 patients who underwent to Auto-SCT. IL28 and IFNΔ4 SNPs were correlated with CMV reactivation along with other clinical and treatment parameters. CMV reactivation by CMV DNAemia was evaluated once a week until day 100 from Auto-SCT. CMV reactivation was documented in 50% (TT-ΔG/ΔG), 35% (CC-TT/TT) and 29.2% (CT-TT/ΔG) of the patients respectively. No differences in CMV copies number were recorded at reactivation between different IL28/IFNλ4 genotypes. The analysis of patients older than 60 years showed a significantly higher incidence of active CMV infection in the TT-ΔG/ΔG (83%) population with respect to CC-TT/TT (21%) and CT-TT/ΔG (40%) patients. Our data suggest a negative role of TT-ΔG/ΔG genotype in the CMV reactivation in Auto-SCT. The exposure to rituximab and the pre-infusion presence of anti CMV IgG also significantly influenced CMV reactivation.

Indexed as

Polymorphism, Single NucleotideAdolescentAdultAgedAllelesCytomegalovirusCytomegalovirus InfectionsFemaleGenotypeHematopoietic Stem Cell TransplantationHumansInterferon LambdaInterferonsInterleukinsLymphoma, Non-HodgkinMaleInterferon Lambdainterferon-lambda, humanInterferonsInterleukins

Identifiers

PMID30036376
PMCPMC6056038
OpenAlexW2884802369

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.