Evidence map›Paper›PMID 19426225›Full record

ReviewImmunological reviews2009

Immunoregulation by tumor necrosis factor superfamily member LIGHT.

Yugang Wang, Mingzhao Zhu, Mendy Miller, Yang-Xin Fu

Open access · greenAbstract readReview
In one paragraph

Review in Immunological reviews, 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
1.0field-weighted citation impact, top 25% 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, 42 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

4 authors at 1 institution in 1 country.

Yugang WangThe Department of Pathology and Committee on Immunology, The University of Chicago, Chicago, IL 60637, USA.
Mingzhao Zhu
Mendy Miller
Yang-Xin Fu
University of Chicago · US

Funding

Synergy of Radiation and Immunotherapy: New ApproachesR01CA134563 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MALTER, JAMES S · 2010 to 2019
$3.4M
Development and Function of Lymphoid TissuesR01AI062026 · NIAID · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 2004 to 2008
$1.6M
Enhanced Immunity Inside of Tumor MicroenvironmentR01CA115540 · NCI · UNIVERSITY OF CHICAGO · PI FU, YANG-XIN · 2006 to 2010
$1.6M
CO-FACILITATORS: NOVEL REGULATORS OF HORMONE METABOLISMR01DK058891 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI ADAMS, JOHN S. · 2001 to 2004
$1.3M
NCI NIH HHS CA115540NCI NIH HHS R01 CA115540NCI NIH HHS R01 CA134563NIAID NIH HHS AI062026NIAID NIH HHS R01 AI062026NIDDK NIH HHS DK58891NIDDK NIH HHS R01 DK058891
6 · The paper itself

Abstract

summaryLIGHT (homologous to lymphotoxins, inducible expression, competes with herpesvirus glycoprotein D for herpesvirus entry mediator, a receptor expressed on T lymphocytes) is a member of the tumor necrosis factor superfamily that contributes to the regulation of immune responses. LIGHT can influence T-cell activation both directly and indirectly by engagement of various receptors that are expressed on T cells and on other types of cells. LIGHT, LIGHT receptors, and their related binding partners constitute a complicated molecular network in the regulation of various processes. The molecular cross-talk among LIGHT and its related molecules presents challenges and opportunities for us to study and to understand the full extent of the LIGHT function. Previous research from genetic and functional studies has demonstrated that dysregulation of LIGHT expression can result in the disturbance of T-cell homeostasis and activation, changing the ability of self-tolerance and of the control of infection. Meanwhile, blockade of LIGHT activity can ameliorate the severity of various T-cell-mediated diseases. These observations indicate the importance of LIGHT and its involvement in many physiological and pathological conditions. Understanding LIGHT interactions offers promising new therapeutic strategies that target LIGHT-engaged pathways to fight against cancer and various infectious diseases.

Indexed as

AnimalsAtherosclerosisDendritic CellsGraft vs Host DiseaseHumansImmunotherapyKiller Cells, NaturalLymphocyte ActivationLymphotoxin beta ReceptorMiceNeoplasmsOrgan TransplantationReceptors, ImmunologicReceptors, Tumor Necrosis Factor, Member 14T-Lymphocyte SubsetsTumor Necrosis Factor Ligand Superfamily Member 14BTLA protein, mouseLymphotoxin beta ReceptorReceptors, ImmunologicReceptors, Tumor Necrosis Factor, Member 14Tumor Necrosis Factor Ligand Superfamily Member 14

Identifiers

PMID19426225
PMCPMC4634935
OpenAlexW2027991051

What OpenQuestion holds

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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.