Evidence map›Paper›PMID 28623307›Full record

ArticleScientific reports2017

Both interferon alpha and lambda can reduce all intrahepatic HDV infection markers in HBV/HDV infected humanized mice.

Katja Giersch, Maria Homs, Tassilo Volz, Martina Helbig, Lena Allweiss, Ansgar W Lohse, Jörg Petersen, Maria Buti, Teresa Pollicino, Camille Sureau and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 63 citations in OpenAlex.

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  11. Hepatocellular Carcinoma in Mongolia Delineates Unique Molecular Traits and a Mutational Signature Associated with Environmental Agents.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
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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

12 authors at 5 institutions in 4 countries.

Katja GierschI. Department of Internal Medicine, University Medical Hospital Hamburg-Eppendorf, Hamburg, Germany.
Maria HomsHospital Vall d'Hebron, Barcelona, Spain.
Tassilo VolzI. Department of Internal Medicine, University Medical Hospital Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-3120-8958
Martina HelbigI. Department of Internal Medicine, University Medical Hospital Hamburg-Eppendorf, Hamburg, Germany.
Lena AllweissI. Department of Internal Medicine, University Medical Hospital Hamburg-Eppendorf, Hamburg, Germany.
Ansgar W LohseI. Department of Internal Medicine, University Medical Hospital Hamburg-Eppendorf, Hamburg, Germany.
Jörg PetersenIFI Institute for Interdisciplinary Medicine at Asklepios Clinic St. Georg, Hamburg, Germany.
Maria ButiHospital Vall d'Hebron, Barcelona, Spain.
Teresa PollicinoDepartment of Human Pathology, University of Messina, Messina, Italy.
Camille SureauInstitut National de la Transfusion Sanguine, Paris, France.
Maura DandriI. Department of Internal Medicine, University Medical Hospital Hamburg-Eppendorf, Hamburg, Germany. m.dandri@uke.de.
Marc LütgehetmannI. Department of Internal Medicine, University Medical Hospital Hamburg-Eppendorf, Hamburg, Germany. mluetgeh@uke.de.ORCID 0000-0002-9468-7944
Universität Hamburg · DEVall d'Hebron Hospital Universitari · ESInstitute for Interdisciplinary Medicine · DEInstitut National de la Transfusion Sanguine · FRUniversity of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Co-infection with hepatitis B (HBV) and D virus (HDV) is associated with the most severe course of liver disease. Interferon represents the only treatment currently approved. However, knowledge about the impact of interferons on HDV in human hepatocytes is scant. Aim was to assess the effect of pegylated interferon alpha (peg-IFNα) and lambda (peg-IFNλ), compared to the HBV-polymerase inhibitor entecavir (ETV) on all HDV infection markers using human liver chimeric mice and novel HDV strand-specific qRT-PCR and RNA in situ hybridization assays, which enable intrahepatic detection of HDV RNA species. Peg-IFNα and peg-IFNλ reduced HDV viremia (1.4 log and 1.2 log, respectively) and serum HBsAg levels (0.9-log and 0.4-log, respectively). Intrahepatic quantification of genomic and antigenomic HDV RNAs revealed a median ratio of 22:1 in untreated mice, resembling levels determined in HBV/HDV infected patients. Both IFNs greatly reduced intrahepatic levels of genomic and antigenomic HDV RNA, increasing the amounts of HDAg- and antigenomic RNA-negative hepatocytes. ETV-mediated suppression of HBV replication (2.1-log) did not significantly affect HBsAg levels, HDV productivity and/or release. In humanized mice lacking adaptive immunity, IFNs but not ETV suppressed HDV. Viremia decrease reflected the intrahepatic reduction of all HDV markers, including the antigenomic template, suggesting that intracellular HDV clearance is achievable.

Indexed as

Hepatitis BHepatitis DAnimalsBiomarkersCoinfectionDisease Models, AnimalGuanineHepatitis B virusHepatitis Delta VirusHeterograftsHumansInterferon-alphaLiver TransplantationMiceTransplantation ChimeraBiomarkersentecavirGuanineInterferon-alpha

Identifiers

PMID28623307
PMCPMC5473824
OpenAlexW2626081703

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.