Evidence map›Paper›PMID 40181970›Full record

ArticleFrontiers in immunology2025

Autoantibodies to apolipoprotein A-I in hepatitis C virus infection: a role in disease progression?

Simon H Bridge, Sabrina Pagano, John K Lodge, Isaac T Shawa, Paula Marin-Crespo, Matthew E Cramp, David A Sheridan, Simon D Taylor-Robinson, Nicolas Vuilleumier, R Dermot G Neely and 1 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Simon H BridgeFaculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, United Kingdom.
Sabrina PaganoDivision of Laboratory Medicine, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.
John K LodgeSchool of Human Sciences, London Metropolitan University, London, United Kingdom.
Isaac T ShawaFaculty of Health, Peninsula Medical School, Plymouth University, Plymouth, United Kingdom.
Paula Marin-CrespoFaculty of Health and Life Sciences, Northumbria University, Newcastle upon Tyne, United Kingdom.
Matthew E CrampFaculty of Health, Peninsula Medical School, Plymouth University, Plymouth, United Kingdom.
David A SheridanFaculty of Health, Peninsula Medical School, Plymouth University, Plymouth, United Kingdom.
Simon D Taylor-RobinsonDepartment of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, United Kingdom.
Nicolas VuilleumierDivision of Laboratory Medicine, Diagnostics Department, Geneva University Hospitals, Geneva, Switzerland.
R Dermot G NeelyDepartment of Blood Sciences, Newcastle upon Tyne Hospitals NHS Foundations Trust, Newcastle upon Tyne, United Kingdom.
Margaret F BassendineTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: Chronic HCV (CHC) infection is associated with autoimmunity. IgG autoantibodies to apolipoprotein A-I (AAA-I) predict all-cause mortality. We evaluated AAA-I in CHC patients and in those who were not viraemic, either because of spontaneous resolution (SR) of infection or HCV clearance following sustained virological response (SVR) after interferon therapy. We limited the study to HCV genotypes 1 and 3, the dominant HCV genotypes circulating in the UK. Methods: Serum samples from 126 CHC patients and 114 nonviraemic individuals (25 SR and 89 SVR) were assayed for AAA-I and lipoproteins. AUC was calculated for AAA-I and HDL-related parameters and used to predict cirrhosis. Fibronectin (FN) and FN-mRNA were measured in human hepatic stellate cells (LX-2) in the presence or absence of AAA-I. Results: AAA-I was found in 47% of patients with CHC, 37% of SVR patients, and 16% of SR individuals (CHC vs. SR, Conclusions: CHC is often associated with AAA-I, and these can persist after SVR. AAA-I is a robust predictor of cirrhosis in CHC infection. LX-2 cells exposed to AAA-I showed increased FN. Further studies are warranted to define the role of AAA-I in promoting not only viral persistence but also fibrosis.

Indexed as

Apolipoprotein A-IAutoantibodiesHepacivirusHepatitis C, ChronicAdultAgedBiomarkersDisease ProgressionFemaleHumansLiver CirrhosisMaleMiddle AgedApolipoprotein A-IAutoantibodiesBiomarkersapolipoprotein A-Iautoantibodiescirrhosisdisease progressionhepatitis C virus (HCV)

Identifiers

PMID40181970
PMCPMC11965114

What OpenQuestion holds

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Registered trials

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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.