Evidence map›Paper›PMID 34188973›Full record

ArticleOncoimmunology2021

Combination blockade of KLRG1 and PD-1 promotes immune control of local and disseminated cancers.

Angela Tata, Garvin Dodard, Céline Fugère, Corinne Leget, Mélody Ors, Benjamin Rossi, Eric Vivier, Laurent Brossay

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed, 38 citations in OpenAlex.

  1. E-cadherin expression promotes tumor growth via KLRG1-dependent pathways.Journal of immunology (Baltimore, Md. : 1950) · 2026
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  12. The role of KLRG1: a novel biomarker and new therapeutic target.Cell communication and signaling : CCS · 2024
    Review
  13. KLRG1 Cell Depletion as a Novel Therapeutic Strategy in Patients with Mature T-Cell Lymphoma Subtypes.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
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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

8 authors at 3 institutions in 2 countries.

Angela TataDepartment of Molecular Microbiology and Immunology, Division of Biology and Medicine, Brown University Alpert Medical School, Providence, Rhode Island, USA.ORCID 0000-0001-9534-4663
Garvin DodardDepartment of Molecular Microbiology and Immunology, Division of Biology and Medicine, Brown University Alpert Medical School, Providence, Rhode Island, USA.ORCID 0000-0003-3464-6443
Céline FugèreDepartment of Molecular Microbiology and Immunology, Division of Biology and Medicine, Brown University Alpert Medical School, Providence, Rhode Island, USA.
Corinne LegetInnate Pharma Research Labs., Marseille, France.
Mélody OrsInnate Pharma Research Labs., Marseille, France.
Benjamin RossiInnate Pharma Research Labs., Marseille, France.
Eric VivierInnate Pharma Research Labs., Marseille, France.ORCID 0000-0001-7022-8287
Laurent BrossayDepartment of Molecular Microbiology and Immunology, Division of Biology and Medicine, Brown University Alpert Medical School, Providence, Rhode Island, USA.ORCID 0000-0002-7497-8488
Brown University · USInnate Pharma (France) · FRAix-Marseille Université · FR

Funding

NK T Cell Interactions with NK Cells During Viral InfectionR01AI046709 · NIAID · BROWN UNIVERSITY · PI BROSSAY, LAURENT · 2001 to 2022
$8.0M
Brown Respiratory Research Training ProgramT32HL134625 · NHLBI · BROWN UNIVERSITY · PI Elizabeth O Harrington, Sharon Irene Smith Rounds · 2017 to 2026
$5.1M
Regulation of MCMV Persistence by Natural Killer CellsR01AI122217 · NIAID · BROWN UNIVERSITY · PI BROSSAY, LAURENT · 2016 to 2020
$2.3M
KLRG1 as a novel target for immune checkpoint blockadeF31CA243305 · NCI · BROWN UNIVERSITY · PI TATA, ANGELA · 2019 to 2020
$88k
NCI NIH HHS F31 CA243305NHLBI NIH HHS T32 HL134625NIAID NIH HHS R01 AI046709NIAID NIH HHS R01 AI122217
6 · The paper itself

Abstract

Checkpoint blockade therapy is effective against many cancers; however, new targets need to be identified to treat patients who do not respond to current treatment or demonstrate immune escape. Here, we showed that blocking the inhibitory receptor Killer cell lectin-like receptor G1 (KLRG1) enhances anti-tumor immunity mediated by NK cells and CD8

Indexed as

NeoplasmsProgrammed Cell Death 1 ReceptorAnimalsCD8-Positive T-LymphocytesHumansImmune Checkpoint InhibitorsImmunotherapyKiller Cells, NaturalLectins, C-TypeMiceReceptors, ImmunologicTumor MicroenvironmentImmune Checkpoint InhibitorsKLRG1 protein, humanKlrg1 protein, mouseLectins, C-TypeProgrammed Cell Death 1 ReceptorReceptors, ImmunologiccancercheckpointKLRG1NK cellsPD-1

Identifiers

PMID34188973
PMCPMC8208121
OpenAlexW3167123091

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.