Evidence map›Paper›PMID 20421498›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

B cell gene signature with massive intrahepatic production of antibodies to hepatitis B core antigen in hepatitis B virus-associated acute liver failure.

Patrizia Farci, Giacomo Diaz, Zhaochun Chen, Sugantha Govindarajan, Ashley Tice, Liane Agulto, Stefania Pittaluga, Denali Boon, Claro Yu, Ronald E Engle and 4 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

86 citing papers in PubMed, 121 citations in OpenAlex.

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  12. Viral etiologies of acute liver failure.World journal of virology · 2024
    Review
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  15. The Role of Carbamoyl Phosphate Synthetase 1 as a Prognostic Biomarker in Patients With Acetaminophen-induced Acute Liver Failure.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2023
    Article
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26 more citing papers are in PubMed but not listed here.

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 7 institutions in 2 countries.

Patrizia FarciLaboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA. pfarci@niaid.nih.gov
Giacomo Diaz
Zhaochun Chen
Sugantha Govindarajan
Ashley Tice
Liane Agulto
Stefania Pittaluga
Denali Boon
Claro Yu
Ronald E Engle
Mark Haas
Richard Simon
Robert H Purcell
Fausto Zamboni
National Institutes of Health · USNational Institute of Allergy and Infectious Diseases · USAzienda Ospedaliera G. Brotzu · ITCedars-Sinai Medical Center · USNational Cancer Institute · USRancho Research Institute · USUniversity of Cagliari · IT

Funding

Molecular Mechanisms of Pathogenesis of Acute and Chronic Liver DiseasesZIAAI000999 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FARCI, PATRIZIA · 2009 to 2025
$25.3M
Pathogenesis of Parenteral Viral HepatitisZIAAI001015 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI PURCELL, ROBERT H. · 2009 to 2012
$3.0M
Intramural NIH HHS
6 · The paper itself

Abstract

Hepatitis B virus (HBV)-associated acute liver failure (ALF) is a dramatic clinical syndrome due to a sudden loss of hepatic cells leading to multiorgan failure. The mechanisms whereby HBV induces ALF are unknown. Here, we show that liver tissue collected at the time of liver transplantation in two patients with HBV-associated ALF is characterized by an overwhelming B cell response apparently centered in the liver with massive accumulation of plasma cells secreting IgG and IgM, accompanied by complement deposition. We demonstrate that the molecular target of these antibodies is the hepatitis B core antigen (HBcAg); that these anti-bodies display a restricted variable heavy chain (V(H)) repertoire and lack somatic mutations; and that these two unrelated individuals with ALF use an identical predominant V(H) gene with unmutated variable domain (IGHV1-3) for both IgG and IgM anti-HBc antibodies, indicating that HBcAg is the target of a germline human V(H) gene. These data suggest that humoral immunity may exert a primary role in the pathogenesis of HBV-associated ALF.

Indexed as

Gene Expression ProfilingB-LymphocytesCell LineageCluster AnalysisComplement System ProteinsDisease ProgressionHepatitis BHepatitis B AntibodiesHepatitis B Core AntigensHepatitis B virusHumansImmunoglobulin GImmunoglobulin MImmunohistochemistryLiverLiver Failure, AcuteComplement System ProteinsHepatitis B AntibodiesHepatitis B Core AntigensImmunoglobulin GImmunoglobulin M

Identifiers

PMID20421498
PMCPMC2889296
OpenAlexW2159616534

What OpenQuestion 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 OpenQuestion graph.