Evidence map›Paper›PMID 19495760›Full record

ReviewSeminars in immunopathology2009

Regulating the mucosal immune system: the contrasting roles of LIGHT, HVEM, and their various partners.

Marcos W Steinberg, Jr-Wen Shui, Carl F Ware, Mitchell Kronenberg

Abstract readReview
In one paragraph

Review in Seminars in immunopathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. The Immunogenetics of Autoimmune Cholestasis.Clinics in liver disease · 2016
    Review
  12. Article
  13. Genetics in PSC: what do the "risk genes" teach us?Clinical reviews in allergy & immunology · 2015
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Marcos W SteinbergDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
Jr-Wen Shui
Carl F Ware
Mitchell Kronenberg
La Jolla Institute for Immunology · US

Funding

Using polygenic scores to enhance both variant discovery, and understanding of functional consequences of genetic variation in IBD.P01DK046763 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI MCGOVERN, DERMOT PATRICK · 1992 to 2020
$31.1M
The role of LIGHT in Colitis PathogenesisR01AI061516 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL · 2004 to 2015
$4.5M
HVEM-BTLA system in InflammationR01AI067890 · NIAID · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI WARE, CARL F · 2007 to 2016
$4.3M
Lymphotoxin alpha Beta and LIGHT cytokine systemsR37AI033068 · NIAID · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI WARE, CARL F · 2003 to 2012
$4.2M
The UCSD Digestive Diseases Research Development CenterR24DK080506 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ECKMANN, LARS · 2008 to 2012
$2.7M
The role of HVEM in inflammation and T cell FunctionF32DK082249 · NIDDK · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SHUI, JRWEN · 2008 to 2010
$127k
NIAID NIH HHS AI06789001NIAID NIH HHS AI61516NIAID NIH HHS R01 AI061516NIAID NIH HHS R01 AI067890NIAID NIH HHS R37 AI033068NIDDK NIH HHS DK 080506NIDDK NIH HHS DK082249NIDDK NIH HHS F32 DK082249NIDDK NIH HHS P01 DK046763NIDDK NIH HHS R24 DK080506
6 · The paper itself

Abstract

LIGHT and herpes virus entry mediator (HVEM) comprise a ligand-receptor pair in the tumor necrosis factor superfamily. These molecules play an important role in regulating immunity, particularly in the intestinal mucosa. LIGHT also binds the lymphotoxin beta receptor, and HVEM can act as a ligand for immunoglobulin family molecules, including B- and T-lymphocyte attenuator, which suppresses immune responses. Complexity in this pivotal system arises from several factors, including the non-monogamous pairing of ligands and receptors, and reverse signaling or the ability of some ligands to serve as receptors. As a result, recognition events in this fascinating network of interacting molecules can have pro- or anti-inflammatory consequences. Despite complexity, experiments we and others are carrying out are establishing rules for understanding when and in what cell types these molecules contribute to intestinal inflammation.

Indexed as

Immunity, MucosalAnimalsB-LymphocytesHumansInflammationIntestinal MucosaReceptors, Tumor Necrosis Factor, Member 14T-LymphocytesTumor Necrosis Factor Ligand Superfamily Member 14Receptors, Tumor Necrosis Factor, Member 14TNFRSF14 protein, humanTNFSF14 protein, humanTumor Necrosis Factor Ligand Superfamily Member 14

Identifiers

PMID19495760
PMCPMC2766922
OpenAlexW1994957830

What OpenQuestion holds

Textmetadata
LicenceTDM
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.