Evidence map›Paper›PMID 42164495›Full record

ArticleFrontiers in immunology2026

Antigen-specific tolerance and control of autoimmunity effected by liver sinusoidal endothelial cells is unimpaired in liver fibrosis.

Cornelia Gottwick, Pia Averhoff, Christian Casar, Laura Anne Liebig, Sabrina Melanie Pilz, Victor Haas, Daria Krzikalla, Sabine Fleischer, Norbert Hübner, Lorenz Adlung and 4 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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.

Cornelia GottwickDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Pia AverhoffDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Christian CasarDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Laura Anne LiebigDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Sabrina Melanie PilzDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Victor HaasDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Daria KrzikallaTopas Therapeutics GmbH, Hamburg, Germany.
Sabine FleischerTopas Therapeutics GmbH, Hamburg, Germany.
Norbert HübnerMax Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
Lorenz AdlungDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Dorothee SchwingeDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Christoph SchrammDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Antonella CarambiaDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Johannes HerkelDepartment of Medicine I, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: Liver sinusoidal endothelial cells (LSECs) have a key role in maintaining organismal homeostasis by scavenging blood-borne molecules and inducing specific immune tolerance to ingested antigens. The scavenger and tolerance function of LSECs can be harnessed for specific treatment of autoimmune diseases by nanoparticle-mediated autoantigen delivery to LSECs. In liver fibrosis, which is a frequent condition in human populations, LSECs undergo changes promoting pro-fibrotic and pro-inflammatory activation of other hepatic cells, but it is unclear whether the scavenger and immune tolerance functions of LSECs are affected. Methods: Utilizing two mouse models of liver fibrosis, we explored the ability of LSECs to take up nanoparticles conjugated with antigen peptides, to present the ingested antigen peptides to T cells and to induce peptide-specific immune tolerance Results: LSECs from fibrotic livers showed few distinct adaptations regarding immune functions; however, overall LSEC identity was largely maintained. Accordingly, endocytosis of nanoparticles by LSECs Conclusions: Scavenger activity and antigen-specific tolerance induction by LSECs are preserved in liver fibrosis. Thus, LSECs remain reliable mediators of homeostasis and tolerance under fibrotic conditions, and particularly suitable targets for nanomedicine products.

Indexed as

AutoantigensAutoimmunityEndothelial CellsImmune ToleranceLiverLiver CirrhosisAnimalsDisease Models, AnimalHumansMiceMice, Inbred C57BLNanoparticlesT-Lymphocytes, RegulatoryAutoantigensautoimmunityimmune toleranceliver fibrosisnanomedicinescavenging

Identifiers

PMID42164495
PMCPMC13183527

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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.