Evidence map›Paper›PMID 38878777›Full record

ArticleCell2024

NLRC5 senses NAD

Balamurugan Sundaram, Nagakannan Pandian, Hee Jin Kim, Hadia M Abdelaal, Raghvendra Mall, Omkar Indari, Roman Sarkar, Rebecca E Tweedell, Emily Q Alonzo, Jonathon Klein and 3 more

Abstract read
In one paragraph

Article in Cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 141 papers.

0numbers the graph read from it
0cells of the map it votes in
141citing papers in PubMed
–field-weighted citation impact
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

141 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. NLRC5-Deficient Macrophages Promote a Tumor-Permissive Phenotype via AXL- and MERTK-Mediated Efferocytosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  13. Innate immunity: current understandings and future perspectives.Signal transduction and targeted therapy · 2026
    Review
  14. Stress Hyperglycemia Drives CD4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  15. Article
  16. Article
  17. The PANoptosis hypothesis examined.Nature reviews. Molecular cell biology · 2026
    Article
  18. Article
  19. Single-cell evidence for PANoptosome complexes.Nature reviews. Molecular cell biology · 2026
    Article
  20. PANoptosis and Immune Remodeling in the Tumor Microenvironment.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review

81 more citing papers are in PubMed but not listed here.

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.

Balamurugan SundaramDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Nagakannan PandianDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Hee Jin KimDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Hadia M AbdelaalDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Raghvendra MallDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Omkar IndariDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Roman SarkarDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Rebecca E TweedellDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Emily Q AlonzoDepartment of Research and Development, Cell Signaling Technology, Danvers, MA 01915, USA.
Jonathon KleinCenter for Advanced Genome Engineering, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Shondra M Pruett-MillerCenter for Advanced Genome Engineering, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Peter VogelAnimal Resources Center and the Veterinary Pathology Core, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Thirumala-Devi KannegantiDepartment of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. Electronic address: thirumala-devi.kanneganti@stjude.org.

Funding

Innate immune sensors, inflammasomes, and inflammasome-mediated processes in cancerR35CA253095 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Thirumala-Devi Kanneganti · 2020 to 2026
$7.0M
Role of NLR Inflammasomes in Autoinflammatory Diseases and Host DefenseR01AR056296 · NIAMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KANNEGANTI, THIRUMALA-DEVI · 2008 to 2022
$5.9M
The Non-Inflammasome NLRs in Immunity and Host defenseR01AI124346 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Thirumala-Devi Kanneganti · 2016 to 2026
$5.8M
Inflammatory Caspases in Innate Immunity and InflammationR37AI101935 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Thirumala-Devi Kanneganti · 2017 to 2026
$4.9M
Targeting innate immune pathways, and inflammatory cell death in cytokine-mediated diseasesR01AI160179 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KANNEGANTI, THIRUMALA-DEVI · 2021 to 2025
$4.2M
Inflammatory Caspases in Innate Immunity and InflammationR01AI101935 · NIAID · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI KANNEGANTI, THIRUMALA-DEVI · 2012 to 2016
$2.2M
NCI NIH HHS R35 CA253095NIAID NIH HHS R01 AI101935NIAID NIH HHS R01 AI124346NIAID NIH HHS R01 AI160179NIAID NIH HHS R37 AI101935NIAMS NIH HHS R01 AR056296
6 · The paper itself

Abstract

NLRs constitute a large, highly conserved family of cytosolic pattern recognition receptors that are central to health and disease, making them key therapeutic targets. NLRC5 is an enigmatic NLR with mutations associated with inflammatory and infectious diseases, but little is known about its function as an innate immune sensor and cell death regulator. Therefore, we screened for NLRC5's role in response to infections, PAMPs, DAMPs, and cytokines. We identified that NLRC5 acts as an innate immune sensor to drive inflammatory cell death, PANoptosis, in response to specific ligands, including PAMP/heme and heme/cytokine combinations. NLRC5 interacted with NLRP12 and PANoptosome components to form a cell death complex, suggesting an NLR network forms similar to those in plants. Mechanistically, TLR signaling and NAD

Indexed as

InflammationIntracellular Signaling Peptides and ProteinsNADAnimalsApoptosis Regulatory ProteinsCalcium-Binding ProteinsCytokinesHEK293 CellsHumansImmunity, InnateInflammasomesMaleMiceMice, Inbred C57BLMice, KnockoutReactive Oxygen SpeciesApoptosis Regulatory ProteinsCalcium-Binding ProteinsCytokinesInflammasomesIntracellular Signaling Peptides and ProteinsIpaf protein, mouseNADNLRC5 protein, humanNLRC5 protein, mouseReactive Oxygen SpeciesToll-Like ReceptorsapoptosisASCcaspasecolitisDAMPhemehemophagocytic lymphohistiocytosisinflammasomeinflammatory cell deathnecroptosisNLRC5NLRP12NLRP3PAMPPANoptosispyroptosisRIPK3ROSTLRsTNF

Identifiers

PMID38878777
PMCPMC11283362

What OpenQuestion holds

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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.