Evidence map›Paper›PMID 21416464›Full record

ArticleEuropean journal of immunology2011

Vstm3 is a member of the CD28 family and an important modulator of T-cell function.

Steven D Levin, David W Taft, Cameron S Brandt, Christoph Bucher, Edward D Howard, Eric M Chadwick, Janet Johnston, Angela Hammond, Kristen Bontadelli, Daniel Ardourel and 14 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 196 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
196citing papers in PubMed, 3 pooled it
3.1field-weighted citation impact, top 8% 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

196 citing papers in PubMed, 3 syntheses or guidelines pooled it, 340 citations in OpenAlex.

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  16. Epitranscriptomics Regulation of CD70, CD80, and TIGIT in Cancer Immunity.International journal of molecular sciences · 2025
    Article
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136 more citing papers are in PubMed but not listed here.

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

24 authors at 1 institution in 1 country.

Steven D LevinDepartment of Immunology, ZymoGenetics, Inc., Seattle, WA, USA. svlv@novonordisk.com
David W Taft
Cameron S Brandt
Christoph Bucher
Edward D Howard
Eric M Chadwick
Janet Johnston
Angela Hammond
Kristen Bontadelli
Daniel Ardourel
LuAnn Hebb
Anitra Wolf
Thomas R Bukowski
Mark W Rixon
Joseph L Kuijper
Craig D Ostrander
James W West
Janine Bilsborough
Brian Fox
Zeren Gao
Wenfeng Xu
Fred Ramsdell
Bruce R Blazar
Katherine E Lewis
University of Minnesota · US

Funding

Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
Project 3: Humoral Targets and B Cell Biology in Chronic Graft-vs.-Host DiseaseP01CA142106 · NCI · DANA-FARBER CANCER INST · PI CUTLER, COREY S · 2009 to 2019
$17.5M
IN VIVO PREVENTION OF MURINE GVHDR01AI034495 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1993 to 2016
$6.2M
T-CELL TARGETING FOR GVHDR01HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1995 to 2022
$5.4M
NCI NIH HHS P01 CA142106NHLBI NIH HHS R01 HL056067NIAID NIH HHS P01 AI056299NIAID NIH HHS R01 AI034495
6 · The paper itself

Abstract

Members of the CD28 family play important roles in regulating T-cell functions and share a common gene structure profile. We have identified VSTM3 as a protein whose gene structure matches that of the other CD28 family members. This protein (also known as TIGIT and WUCAM) has been previously shown to affect immune responses and is expressed on NK cells, activated and memory T cells, and Tregs. The nectin-family proteins CD155 and CD112 serve as counter-structures for VSTM3, and CD155 and CD112 also bind to the activating receptor CD226 on T cells and NK cells. Hence, this group of interacting proteins forms a network of molecules similar to the well-characterized CD28-CTLA-4-CD80-CD86 network. In the same way that soluble CTLA-4 can be used to block T-cell responses, we show that soluble Vstm3 attenuates T-cell responses in vitro and in vivo. Moreover, animals deficient in Vstm3 are more sensitive to autoimmune challenges indicating that this new member of the CD28 family is an important regulator of T-cell responses.

Indexed as

AnimalsAutoimmune DiseasesCD28 AntigensCells, CulturedDendritic CellsHumansMiceRatsReceptors, ImmunologicT-LymphocytesCD28 AntigensReceptors, ImmunologicT cell Ig and ITIM domain protein, mouseTIGIT protein, humanTIGIT protein, rat

Identifiers

PMID21416464
PMCPMC3733993
OpenAlexW1972338421

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.