Evidence map›Paper›PMID 26861112›Full record

ArticleNature communications2016

NLRC5 shields T lymphocytes from NK-cell-mediated elimination under inflammatory conditions.

Kristina Ludigs, Camilla Jandus, Daniel T Utzschneider, Francesco Staehli, Stéphanie Bessoles, Anh Thu Dang, Giorgia Rota, Wilson Castro, Dietmar Zehn, Eric Vivier and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

36 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Humanization of Drug Metabolism in theACS infectious diseases · 2025
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  3. Review
  4. Article
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  6. Review
  7. Negativity begets longevity in T cells.The Journal of clinical investigation · 2023
    Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Targeting natural killer cells to enhance vaccine responses.Trends in pharmacological sciences · 2021
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. NLRC5: new cancer buster?Molecular biology reports · 2020
    Review
  19. Article
  20. 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

13 authors at 3 institutions in 2 countries.

Kristina LudigsDepartment of Biochemistry, University of Lausanne, Epalinges 1066, Switzerland.
Camilla JandusLudwig Center for Cancer Research of the University of Lausanne, Epalinges 1066, Switzerland.
Daniel T UtzschneiderDivision of Allergology and Immunology, CHUV, University of Lausanne, Epalinges 1066, Switzerland.
Francesco StaehliDepartment of Biochemistry, University of Lausanne, Epalinges 1066, Switzerland.
Stéphanie BessolesLudwig Center for Cancer Research of the University of Lausanne, Epalinges 1066, Switzerland.
Anh Thu DangDepartment of Biochemistry, University of Lausanne, Epalinges 1066, Switzerland.
Giorgia RotaDepartment of Biochemistry, University of Lausanne, Epalinges 1066, Switzerland.
Wilson CastroDepartment of Biochemistry, University of Lausanne, Epalinges 1066, Switzerland.
Dietmar ZehnDivision of Allergology and Immunology, CHUV, University of Lausanne, Epalinges 1066, Switzerland.
Eric VivierCentre d'Immunologie de Marseille-Luminy, Aix-Marseille University UM2, Inserm U1104, CNRS UMR7280, Marseille 13288, France.
Werner HeldLudwig Center for Cancer Research of the University of Lausanne, Epalinges 1066, Switzerland.ORCID http://orcid.org/0000-0003-3292-1536
Pedro RomeroLudwig Center for Cancer Research of the University of Lausanne, Epalinges 1066, Switzerland.
Greta GuardaDepartment of Biochemistry, University of Lausanne, Epalinges 1066, Switzerland.
University of Lausanne · CHCentre National de la Recherche Scientifique · FRLudwig Cancer Research · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NLRC5 is a transcriptional regulator of MHC class I (MHCI), which maintains high MHCI expression particularly in T cells. Recent evidence highlights an important NK-T-cell crosstalk, raising the question on whether NLRC5 specifically modulates this interaction. Here we show that NK cells from Nlrc5-deficient mice exhibit moderate alterations in inhibitory receptor expression and responsiveness. Interestingly, NLRC5 expression in T cells is required to protect them from NK-cell-mediated elimination upon inflammation. Using T-cell-specific Nlrc5-deficient mice, we show that NK cells surprisingly break tolerance even towards 'self' Nlrc5-deficient T cells under inflammatory conditions. Furthermore, during chronic LCMV infection, the total CD8(+) T-cell population is severely decreased in these mice, a phenotype reverted by NK-cell depletion. These findings strongly suggest that endogenous T cells with low MHCI expression become NK-cell targets, having thus important implications for T-cell responses in naturally or therapeutically induced inflammatory conditions.

Indexed as

AnimalsAnimals, CongenicArenaviridae InfectionsChlorocebus aethiopsFlow CytometryGene Expression RegulationHistocompatibility Antigens Class IHumansInflammationInterferon InducersIntracellular Signaling Peptides and ProteinsKiller Cells, NaturalLymphocytic choriomeningitis virusMiceMice, Inbred C57BLMice, KnockoutHistocompatibility Antigens Class IInterferon InducersIntracellular Signaling Peptides and ProteinsNLRC5 protein, mousePoly I-C

Identifiers

PMID26861112
PMCPMC4749981
OpenAlexW2403911842

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.