Evidence map›Paper›PMID 39440957›Full record

ReviewMicrobiology and molecular biology reviews : MMBR2024

Hepatitis B virus entry, assembly, and egress.

Yu-Chen Chuang, J-H James Ou

Abstract readReview
In one paragraph

Review in Microbiology and molecular biology reviews : MMBR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. 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

2 authors.

Yu-Chen ChuangDepartment of Molecular Microbiology and Immunology, University of Southern California Keck School of Medicine, Los Angeles, California, USA.ORCID 0000-0001-5726-8583
J-H James OuDepartment of Molecular Microbiology and Immunology, University of Southern California Keck School of Medicine, Los Angeles, California, USA.ORCID 0000-0002-8274-5705

Funding

Maternal effect on offspring immunity against hepatitis B virusR01AI145813 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI AKBARI, OMID, OU, J.-H. JAMES · 2019 to 2023
$3.2M
Hepatitis B virus e antigen in viral persistenceR01AI129540 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OU, J.-H. JAMES · 2017 to 2021
$2.1M
Autophagy and the Replication of Hepatitis B VirusR01AI148304 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OU, J.-H. JAMES · 2020 to 2024
$2.1M
Hepatitis B virus e antigen in viral persistenceR37AI129540 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI J.-H. James Ou · 2023 to 2026
$2.0M
IL-1β as a novel therapeutic agent against hepatitis B virusR21AI179734 · NIAID · UNIVERSITY OF SOUTHERN CALIFORNIA · PI OU, J.-H. JAMES · 2024 to 2025
$445k
HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI129540HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI145813HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI148304HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) AI179734NIAID NIH HHS R01 AI129540NIAID NIH HHS R01 AI145813NIAID NIH HHS R01 AI148304NIAID NIH HHS R21 AI179734NIAID NIH HHS R37 AI129540
6 · The paper itself

Abstract

SUMMARYHepatitis B virus (HBV) is an important human pathogen that chronically infects approximately 250 million people in the world, resulting in ~1 million deaths annually. This virus is a hepatotropic virus and can cause severe liver diseases including cirrhosis and hepatocellular carcinoma. The entry of HBV into hepatocytes is initiated by the interaction of its envelope proteins with its receptors. This is followed by the delivery of the viral nucleocapsid to the nucleus for the release of its genomic DNA and the transcription of viral RNAs. The assembly of the viral capsid particles may then take place in the nucleus or the cytoplasm and may involve cellular membranes. This is followed by the egress of the virus from infected cells. In recent years, significant research progresses had been made toward understanding the entry, the assembly, and the egress of HBV particles. In this review, we discuss the molecular pathways of these processes and compare them with those used by hepatitis delta virus and hepatitis C virus , two other hepatotropic viruses that are also enveloped. The understanding of these processes will help us to understand how HBV replicates and causes diseases, which will help to improve the treatments for HBV patients.

Indexed as

Hepatitis BHepatitis B virusVirus AssemblyVirus InternalizationVirus ReleaseAnimalsHepatocytesHumansNucleocapsidViral Envelope ProteinsVirus ReplicationViral Envelope Proteinsamphisomesautophagyclathrin-mediated endocytosisexocytosishepatitis B virushepatitis C virushepatitis delta virusmultivesicular bodiesviral entry

Identifiers

PMID39440957
PMCPMC11653734

What Socratic holds

Textmetadata
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 Socratic graph.