Evidence map›Paper›PMID 24205056›Full record

ArticlePloS one2013

CD8 T cell memory to a viral pathogen requires trans cosignaling between HVEM and BTLA.

Rachel Flynn, Tarun Hutchinson, Kenneth M Murphy, Carl F Ware, Michael Croft, Shahram Salek-Ardakani

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 57 citations in OpenAlex.

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  14. Accelerator or Brake: Immune Regulators in Malaria.Frontiers in cellular and infection microbiology · 2020
    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

6 authors at 4 institutions in 1 country.

Rachel FlynnDepartment of Pathology, Immunology & Laboratory Medicine, University of Florida, Gainesville, Florida, United States of America ; La Jolla Institute for Allergy and Immunology, Divisions of Immune Regulation, San Diego, California, United States of America.
Tarun Hutchinson
Kenneth M Murphy
Carl F Ware
Michael Croft
Shahram Salek-Ardakani
La Jolla Institute for Immunology · USHoward Hughes Medical Institute · USSanford Burnham Prebys Medical Discovery Institute · USUniversity of Florida · US

Funding

Anti-herpesvirus Signaling by LTalphabeta/LIGHT CytokinesR01AI048073 · NIAID · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI WARE, CARL F · 2001 to 2016
$7.0M
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
Regulation of T Cell Tolerance by OX40R01CA091837 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2002 to 2012
$2.5M
TNFR Members in T Cell Immunity to VacciniaR01AI067341 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2006 to 2010
$2.3M
LIGHT_HVEM_BTLA axis in protective anti_viral immunityR01AI087734 · NIAID · UNIVERSITY OF FLORIDA · PI SALEK-ARDAKANI, SHAHRAM · 2011 to 2015
$1.6M
SURFACE LYMPHOTOXIN A/B COMPLEXESR01AI033068 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI WARE, CARL F · 1994 to 2002
$1.0M
T Cell Memory to Respiratory Viral InfectionsR21AI077079 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SALEK-ARDAKANI, SHAHRAM · 2007 to 2008
$515k
TNFR Members in T Cell Immunity to VacciniaR56AI067341 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2012 to 2012
$348k
NCI NIH HHS CA91837NCI NIH HHS R01 CA091837NIAID NIH HHS AI033068NIAID NIH HHS AI048073NIAID NIH HHS AI067890NIAID NIH HHS AI087734NIAID NIH HHS AI67341NIAID NIH HHS AI77079NIAID NIH HHS R01 AI033068NIAID NIH HHS R01 AI048073NIAID NIH HHS R01 AI067341NIAID NIH HHS R01 AI067890NIAID NIH HHS R01 AI087734NIAID NIH HHS R21 AI077079NIAID NIH HHS R37 AI033068NIAID NIH HHS R56 AI067341
6 · The paper itself

Abstract

Defining the molecular interactions required to program activated CD8 T cells to survive and become memory cells may allow us to understand how to augment anti-viral immunity. HVEM (herpes virus entry mediator) is a member of the tumor necrosis factor receptor (TNFR) family that interacts with ligands in the TNF family, LIGHT and Lymphotoxin-α, and in the Ig family, B and T lymphocyte attenuator (BTLA) and CD160. The Ig family members initiate inhibitory signaling when engaged with HVEM, but may also activate survival gene expression. Using a model of vaccinia virus infection, we made the unexpected finding that deficiency in HVEM or BTLA profoundly impaired effector CD8 T cell survival and development of protective immune memory. Mixed adoptive transfer experiments indicated that BTLA expressed in CD8α+ dendritic cells functions as a trans-activating ligand that delivers positive co-signals through HVEM expressed in T cells. Our data demonstrate a critical role of HVEM-BTLA bidirectional cosignaling system in antiviral defenses by driving the differentiation of memory CD8 T cells.

Indexed as

AnimalsCD8-Positive T-LymphocytesFemaleFlow CytometryFluorescent Antibody TechniqueLymphocyte ActivationMiceReceptors, ImmunologicReceptors, Tumor Necrosis Factor, Member 14Signal TransductionVaccinia virusBTLA protein, mouseReceptors, ImmunologicReceptors, Tumor Necrosis Factor, Member 14

Identifiers

PMID24205056
PMCPMC3812147
OpenAlexW2031764503

What OpenQuestion holds

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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.