Evidence map›Paper›PMID 29427479›Full record

ReviewLiver international : official journal of the International Association for the Study of the Liver2018

Towards HBV curative therapies.

Raymond F Schinazi, Maryam Ehteshami, Leda Bassit, Tarik Asselah

Abstract readReview
In one paragraph

Review in Liver international : official journal of the International Association for the Study of the Liver, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
–field-weighted citation impact
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

42 citing papers in PubMed.

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  13. Targeting the hepatitis B cccDNA with a sequence-specific ARCUS nuclease to eliminate hepatitis B virus in vivo.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
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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

4 authors.

Raymond F SchinaziCenter for AIDS Research, Emory University School of Medicine, Atlanta, GA, USA.
Maryam EhteshamiCenter for AIDS Research, Emory University School of Medicine, Atlanta, GA, USA.
Leda BassitCenter for AIDS Research, Emory University School of Medicine, Atlanta, GA, USA.
Tarik AsselahDepartment of Hepatology, Centre de Recherche sur l'Inflammation, Viral Hepatitis INSERM UMR 1149, AP-HP Hôpital Beaujon, Université Paris Diderot, Clichy, France.ORCID 0000-0002-0024-0595

Funding

Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Ann M Chahroudi, Colleen F Kelley · 2002 to 2026
$74.0M
HBV Capsid EffectorsR01AI132833 · NIAID · EMORY UNIVERSITY · PI Raymond Felix Schinazi · 2017 to 2026
$5.3M
NIAID NIH HHS P30 AI050409NIAID NIH HHS R01 AI132833
6 · The paper itself

Abstract

Tremendous progress has been made over the last 2 decades to discover and develop approaches to control hepatitis B virus (HBV) infections and to prevent the development of hepatocellular carcinoma using various interferons and small molecules as antiviral agents. However, none of these agents have significant impact on eliminating HBV from infected cells. Currently the emphasis is on silencing or eliminating cccDNA, which could lead to a cure for HBV. Various approaches are being developed including the development of capsid effectors, CRISPR/Cas9, TALENS, siRNA, entry and secretion inhibitors, as well as immunological approaches. It is very likely that a combination of these modalities will need to be employed to successfully eliminate HBV or prevent virus rebound on discontinuation of therapy. In the next 5 years clinical data will emerge which will provide insight on the safety and feasibility of these approaches and if they can be applied to eradicate HBV infections globally. In this review, we summarize current treatments and we highlight and examine recent therapeutic strategies that are currently being evaluated at the preclinical and clinical stage.

Indexed as

ImmunotherapyAntiviral AgentsCRISPR-Associated Protein 9CRISPR-Cas SystemsDNA, CircularDNA, ViralHepatitis BHepatitis B virusHumansRNA, Small InterferingTranscription Activator-Like Effector NucleasesVirus ReplicationAntiviral AgentsCRISPR-Associated Protein 9DNA, CircularDNA, ViralRNA, Small InterferingTranscription Activator-Like Effector Nucleasesantiviral agentscccDNAHBV cureimmunotherapy

Identifiers

PMID29427479
PMCPMC6481632

What OpenQuestion holds

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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.