Evidence map›Paper›PMID 23918985›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2013

Soluble CD80 restores T cell activation and overcomes tumor cell programmed death ligand 1-mediated immune suppression.

Samuel T Haile, Sonia P Dalal, Virginia Clements, Koji Tamada, Suzanne Ostrand-Rosenberg

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

55 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
  2. Novel insights into the effect of sTIM-3 on NLRP3 inflammasome via interacting with ASC.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
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  3. The Ubiquitin-Proteasome System in Brain Disorders: Pathogenic Pathways, Post-Translational Tweaks, and Therapeutic Frontiers.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Review
  4. Article
  5. Article
  6. Review
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  8. Review
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  11. Article
  12. Article
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  14. Article
  15. Targeting Cbl-b in cancer immunotherapy.Journal for immunotherapy of cancer · 2023
    Review
  16. Article
  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

5 authors at 2 institutions in 2 countries.

Samuel T HaileDepartment of Biological Sciences, University of Maryland, Baltimore County, Baltimore, MD 21250, USA.
Sonia P Dalal
Virginia Clements
Koji Tamada
Suzanne Ostrand-Rosenberg
University of Maryland, Baltimore County · USYamaguchi University · JP

Funding

EXPAND PARTICIPATION BY MINORITIES IN BIOMEDICAL SCIENCER25GM055036 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI SUMMERS, MICHAEL FINLEY · 1996 to 2021
$16.9M
Graduate Training at The Chemistry Biology InterfaceT32GM066706 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI SELEY-RADTKE, KATHERINE L, SMITH, AARON T · 2004 to 2023
$3.3M
Cell-based tumor vaccines targeting CD4+ T lymphocytesR01CA084232 · NCI · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI OSTRAND-ROSENBERG, SUZANNE · 2000 to 2011
$2.6M
Tumor-Induced immune suppressionR01CA115880 · NCI · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI OSTRAND-ROSENBERG, SUZANNE · 2006 to 2010
$1.3M
NCI NIH HHS R01 CA084232NCI NIH HHS R01 CA115880NCI NIH HHS R01CA115880NCI NIH HHS R01CA84232NIGMS NIH HHS R25 GM055036NIGMS NIH HHS T32 GM066706
6 · The paper itself

Abstract

Many tumor cells escape anti-tumor immunity through their expression of programmed death ligand-1 (PDL1 or B7-H1), which interacts with T cell-expressed PD1 and results in T cell apoptosis. We previously reported that transfection of human tumor cells with a membrane-bound form of the human costimulatory molecule CD80 prevented PD1 binding and restored T cell activation. We now report that a membrane-bound form of murine CD80 similarly reduces PDL1-PD1-mediated suppression by mouse tumor cells and that a soluble protein consisting of the extracellular domains of human or mouse CD80 fused to the Fc domain of IgG1 (CD80-Fc) overcomes PDL1-mediated suppression by human and mouse tumor cells, respectively. T cell activation experiments with human and mouse tumor cells indicate that CD80-Fc facilitates T cell activation by binding to PDL1 to inhibit PDL1-PD1 interactions and by costimulating through CD28. CD80-Fc is more effective in preventing PD1-PDL1-mediated suppression and restoring T cell activation compared with treatment with mAb to either PD1 or PDL1. These studies identify CD80-Fc as an alternative and potentially more efficacious therapeutic agent for overcoming PDL1-induced immune suppression and facilitating tumor-specific immunity.

Indexed as

AnimalsB7-1 AntigenB7-H1 AntigenBlotting, WesternCell Line, TumorFlow CytometryHumansLymphocyte ActivationMiceMice, Inbred BALB CMice, Inbred C57BLMice, TransgenicNeoplasmsT-LymphocytesTransfectionTumor EscapeB7-1 AntigenB7-H1 Antigen

Identifiers

PMID23918985
PMCPMC3750086
OpenAlexW2097707681

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.