Evidence map›Paper›PMID 30254647›Full record

ReviewFrontiers in immunology2018

Complex Network of NKT Cell Subsets Controls Immune Homeostasis in Liver and Gut.

Idania Marrero, Igor Maricic, Ariel E Feldstein, Rohit Loomba, Bernd Schnabl, Jesus Rivera-Nieves, Lars Eckmann, Vipin Kumar

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed, 47 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Idania MarreroLaboratory of Immune Regulation, University of California, San Diego, La Jolla, CA, United States.
Igor MaricicLaboratory of Immune Regulation, University of California, San Diego, La Jolla, CA, United States.
Ariel E FeldsteinDepartment of Pediatrics, University of California, San Diego, La Jolla, CA, United States.
Rohit LoombaDivision of Gastroenterology and Hepatology, Department of Medicine, University of California, San Diego, La Jolla, CA, United States.
Bernd SchnablDivision of Gastroenterology and Hepatology, Department of Medicine, University of California, San Diego, La Jolla, CA, United States.
Jesus Rivera-NievesDivision of Gastroenterology and Hepatology, Department of Medicine, University of California, San Diego, La Jolla, CA, United States.
Lars EckmannDivision of Gastroenterology and Hepatology, Department of Medicine, University of California, San Diego, La Jolla, CA, United States.
Vipin KumarLaboratory of Immune Regulation, University of California, San Diego, La Jolla, CA, United States.
University of California, San Diego · US

Funding

Sulfatide-reactive type II NKT cells: repertoire and functionR01CA100660 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KUMAR, VIPIN · 2004 to 2014
$3.5M
Novel Traffic-targeted Therapies for IBDR01DK108670 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI RIVERA-NIEVES, JESUS · 2016 to 2020
$3.3M
Interplay Among NKT Cell Subsets in Alcoholic Liver DiseaseR01AA020864 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KUMAR, VIPIN · 2012 to 2016
$1.8M
NCI NIH HHS R01 CA100660NIAAA NIH HHS R01 AA020864NIDDK NIH HHS R01 DK108670
6 · The paper itself

Abstract

The liver-gut immune axis is enriched in several innate immune cells, including innate-like unconventional and adaptive T cells that are thought to be involved in the maintenance of tolerance to gut-derived antigens and, at the same time, enable effective immunity against microbes. Two subsets of lipid-reactive CD1d-restricted natural killer T (NKT) cells, invariant NKT (iNKT) and type II NKT cells present in both mice and humans. NKT cells play an important role in regulation of inflammation in the liver and gut due to their innate-like properties of rapid secretion of a myriad of pro-inflammatory and anti-inflammatory cytokines and their ability to influence other innate cells as well as adaptive T and B cells. Notably, a bi-directional interactive network between NKT cells and gut commensal microbiota plays a crucial role in this process. Here, we briefly review recent studies related to the cross-regulation of both NKT cell subsets and how their interactions with other immune cells and parenchymal cells, including hepatocytes and enterocytes, control inflammatory diseases in the liver, such as alcoholic and non-alcoholic steatohepatitis, as well as inflammation in the gut. Overwhelming experimental data suggest that while iNKT cells are pathogenic, type II NKT cells are protective in the liver. Since CD1d-dependent pathways are highly conserved from mice to humans, a detailed cellular and molecular understanding of these immune regulatory pathways will have major implications for the development of novel therapeutics against inflammatory diseases of liver and gut.

Indexed as

Adaptive ImmunityImmunity, InnateAnimalsAntigens, CD1dGastrointestinal MicrobiomeHumansIntestinesLiverMiceNatural Killer T-CellsAntigens, CD1dCD1D protein, humanCD1depitheliumhepatitislipidsmicrobiota

Identifiers

PMID30254647
PMCPMC6141878
OpenAlexW2889809922

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.