Evidence map›Paper›PMID 37670813›Full record

ReviewImmune network2023

IFN-γ: A Crucial Player in the Fight Against HBV Infection?

Marine Laure Bettina Hillaire, Philip Lawrence, Brice Lagrange

Open access · diamondAbstract readReview
In one paragraph

Review in Immune network, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 18 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

3 authors at 1 institution in 1 country.

Marine Laure Bettina HillaireConfluence: Sciences et Humanités (EA 1598), Université Catholique de Lyon, Lyon, France.ORCID https://orcid.org/0000-0002-3672-3935
Philip LawrenceConfluence: Sciences et Humanités (EA 1598), Université Catholique de Lyon, Lyon, France.ORCID https://orcid.org/0000-0002-7637-045X
Brice LagrangeConfluence: Sciences et Humanités (EA 1598), Université Catholique de Lyon, Lyon, France.ORCID https://orcid.org/0000-0002-4131-5995
Université catholique de lyon · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

About 0.8 million people die because of hepatitis B virus (HBV) infection each year. In around 5% of infected adults, the immune system is ineffective in countering HBV infection, leading to chronic hepatitis B (CHB). CHB is associated with hepatocellular carcinoma, which can lead to patient death. Unfortunately, although current treatments against CHB allow control of HBV infection, they are unable to achieve complete eradication of the virus. Cytokines of the IFN family represent part of the innate immune system and are key players in virus elimination. IFN secretion induces the expression of interferon stimulated genes, producing proteins that have antiviral properties and that are essential to cell-autonomous immunity. IFN-α is commonly used as a therapeutic approach for CHB. In addition, IFN-γ has been identified as the main IFN family member responsible for HBV eradication during acute infection. In this review, we summarize the key evidence gained from cellular or animal models of HBV replication or infection concerning the potential anti-HBV roles of IFN-γ with a particular focus on some IFN-γ-inducible genes.

Indexed as

Chronic infectionHepatitis B virusInnate immunityInterferon-gammaInterferon-stimulated genes

Identifiers

PMID37670813
PMCPMC10475827
OpenAlexW4386297696

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.