Evidence map›Paper›PMID 31937317›Full record

ArticleCell communication and signaling : CCS2020

Targeting the orphan nuclear receptor NR2F6 in T cells primes tumors for immune checkpoint therapy.

Victoria Klepsch, Maria Pommermayr, Dominik Humer, Natascha Brigo, Natascha Hermann-Kleiter, Gottfried Baier

Open access · goldAbstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Loss of NR2F6 Protects from Salmonella Typhimurium Infection.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Regulation of PD-L1 Expression by Nuclear Receptors.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. CRISPR/Cas9 revitalizes adoptive T-cell therapy for cancer immunotherapy.Journal of experimental & clinical cancer research : CR · 2021
    Review
  16. Review
  17. Review
  18. NR2F6 as a Prognostic Biomarker in HNSCC.International journal of molecular sciences · 2020
    Article
  19. Article
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 1 institution in 1 country.

Victoria KlepschDivision of Translational Cell Genetics, Medical University of Innsbruck, Peter Mayr Str. 1a, A-6020, Innsbruck, Austria. Victoria.Klepsch@i-med.ac.at.ORCID 0000-0003-4146-4664
Maria PommermayrDivision of Translational Cell Genetics, Medical University of Innsbruck, Peter Mayr Str. 1a, A-6020, Innsbruck, Austria.
Dominik HumerDivision of Translational Cell Genetics, Medical University of Innsbruck, Peter Mayr Str. 1a, A-6020, Innsbruck, Austria.
Natascha BrigoDivision of Translational Cell Genetics, Medical University of Innsbruck, Peter Mayr Str. 1a, A-6020, Innsbruck, Austria.
Natascha Hermann-KleiterDivision of Translational Cell Genetics, Medical University of Innsbruck, Peter Mayr Str. 1a, A-6020, Innsbruck, Austria.
Gottfried BaierDivision of Translational Cell Genetics, Medical University of Innsbruck, Peter Mayr Str. 1a, A-6020, Innsbruck, Austria. Gottfried.Baier@i-med.ac.at.
Innsbruck Medical University · AT

Funding

Austrian Science Fund FWF P 30324Austrian Science Fund FWF P 31383
6 · The paper itself

Abstract

backgroundNR2F6 has been proposed as an alternative cancer immune checkpoint in the effector T cell compartment. However, a realistic assessment of the in vivo therapeutic potential of NR2F6 requires acute depletion.

methodsEmploying primary T cells isolated from Cas9-transgenic mice for electroporation of chemically synthesized sgRNA, we established a CRISPR/Cas9-mediated acute knockout protocol of Nr2f6 in primary mouse T cells.

resultsAnalyzing these Nr2f6

conclusionsThese findings indicate that Nr2f6

Indexed as

AnimalsBase SequenceCells, CulturedCRISPR-Cas SystemsCTLA-4 AntigenGene DeletionImmune Checkpoint InhibitorsImmunityMice, Inbred C57BLMutagenesisNeoplasmsProgrammed Cell Death 1 ReceptorRepressor ProteinsReproducibility of ResultsRNA, Guide, CRISPR-Cas SystemsT-LymphocytesCTLA-4 AntigenImmune Checkpoint InhibitorsNr2f6 protein, mouseProgrammed Cell Death 1 ReceptorRepressor ProteinsRNA, Guide, CRISPR-Cas SystemsCombinatorial treatment regimensCRISPR/Cas9 genetically modified cell therapyImmune checkpoint NR2F6; transcriptional repressor of CD3+ effector T cell functions

Identifiers

PMID31937317
PMCPMC6961368
OpenAlexW3004774000

What OpenQuestion holds

Textmetadata
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.