Evidence map›Paper›PMID 33311540›Full record

ArticleScientific reports2020

NKT cells promote both type 1 and type 2 inflammatory responses in a mouse model of liver fibrosis.

Julia Nilsson, Maria Hörnberg, Anja Schmidt-Christensen, Kajsa Linde, Maria Nilsson, Marine Carlus, Saskia F Erttmann, Sofia Mayans, Dan Holmberg

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  4. CD2 expressing innate lymphoid and T cells are critical effectors of immunopathogenesis in hidradenitis suppurativa.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  14. Pathogenesis from Inflammation to Cancer in NASH-Derived HCC.Journal of hepatocellular carcinoma · 2022
    Review
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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

9 authors at 2 institutions in 1 country.

Julia NilssonDepartment of Experimental Medical Sciences, Lund University Diabetes Center, Clinical Research Center, Lund University, Jan Waldenströms gata 35, 214 28, Malmö, Sweden.
Maria HörnbergInfiCure Bio AB, Tvistevägen 48 C, 907 36, Umeå, Sweden.
Anja Schmidt-ChristensenDepartment of Experimental Medical Sciences, Lund University Diabetes Center, Clinical Research Center, Lund University, Jan Waldenströms gata 35, 214 28, Malmö, Sweden.
Kajsa LindeInfiCure Bio AB, Tvistevägen 48 C, 907 36, Umeå, Sweden.
Maria NilssonDepartment of Experimental Medical Sciences, Lund University Diabetes Center, Clinical Research Center, Lund University, Jan Waldenströms gata 35, 214 28, Malmö, Sweden.
Marine CarlusCarlus Pathology Consulting, 2 rue de la Libération, 76630, Bellengreville, France.
Saskia F ErttmannDepartment of Molecular Biology, Umeå University, 901 87, Umeå, Sweden.
Sofia MayansInfiCure Bio AB, Tvistevägen 48 C, 907 36, Umeå, Sweden.
Dan HolmbergDepartment of Experimental Medical Sciences, Lund University Diabetes Center, Clinical Research Center, Lund University, Jan Waldenströms gata 35, 214 28, Malmö, Sweden. dan.holmberg@med.lu.se.
Lund University · SEUmeå University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sterile liver inflammation and fibrosis are associated with many liver disorders of different etiologies. Both type 1 and type 2 inflammatory responses have been reported to contribute to liver pathology. However, the mechanisms controlling the balance between these responses are largely unknown. Natural killer T (NKT) cells can be activated to rapidly secrete cytokines and chemokines associated with both type 1 and type 2 inflammatory responses. As these proteins have been reported to accumulate in different types of sterile liver inflammation, we hypothesized that these cells may play a role in this pathological process. We have found that a transgenic NKT (tgNKT) cell population produced in the immunodeficient 2,4αβNOD.Rag2

Indexed as

AnimalsCytokinesDisease Models, AnimalFibrosisHepatitisImmunity, CellularImmunity, InnateInflammasomesLiverLiver CirrhosisLiver DiseasesMaleMiceMice, Inbred NODNatural Killer T-CellsCytokinesInflammasomes

Identifiers

PMID33311540
PMCPMC7732838
OpenAlexW3112029388

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.