Evidence map›Paper›PMID 33746941›Full record

ArticleFrontiers in immunology2021

Soluble N-Acetylgalactosamine-Modified Antigens Enhance Hepatocyte-Dependent Antigen Cross-Presentation and Result in Antigen-Specific CD8

Martina Damo, D Scott Wilson, Elyse A Watkins, Jeffrey A Hubbell

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Epitope-based precision immunotherapy of Type 1 diabetes.Human vaccines & immunotherapeutics · 2023
    Article
  6. Review
  7. Biomaterial Strategies for Selective Immune Tolerance: Advances and Gaps.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  8. Article
  9. 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

4 authors at 3 institutions in 2 countries.

Martina DamoInstitute for Molecular Engineering, University of Chicago, Chicago, IL, United States.
D Scott WilsonInstitute for Molecular Engineering, University of Chicago, Chicago, IL, United States.
Elyse A WatkinsInstitute for Molecular Engineering, University of Chicago, Chicago, IL, United States.
Jeffrey A HubbellInstitute for Molecular Engineering, University of Chicago, Chicago, IL, United States.
École Polytechnique Fédérale de Lausanne · CHBioengineering (Switzerland) · CHUniversity of Chicago · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocytes compose up to 80% of the total liver and have been indicated as important players in the induction of immunologic tolerance in this organ. We show that hepatocytes possess the molecular machinery required for the cross-presentation of extracellular antigens. Using a derivative of the model antigen ovalbumin (OVA) covalently modified with a polymer containing multiple N-acetylgalactosamine residues (pGal-OVA) that enhance extracellular antigen uptake by mimicking the glycome of apoptotic debris, we show efficient hepatocyte-dependent induction of cross-tolerance of both adoptively transferred OT-I cells and endogenous OVA-specific CD8

Indexed as

AcetylgalactosamineAdoptive TransferAnimalsAntigen PresentationAntigensATP Binding Cassette Transporter, Subfamily B, Member 2CD8-Positive T-LymphocytesCells, CulturedCross-PrimingHepatocytesImmune ToleranceMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicOvalbuminAcetylgalactosamineAntigensATP Binding Cassette Transporter, Subfamily B, Member 2early endosome antigen 1OvalbuminTap1 protein, mouseVesicular Transport Proteinsantigen modificationsCD8 T cellcross-presentation/priminghepatocytestolerance

Identifiers

PMID33746941
PMCPMC7965950
OpenAlexW3135627954

What OpenQuestion holds

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LicenceCC BY
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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.