Evidence map›Paper›PMID 35624206›Full record

ArticleNature immunology2022

NLRP3 licenses NLRP11 for inflammasome activation in human macrophages.

Anu Gangopadhyay, Savita Devi, Shivendra Tenguria, Jessica Carriere, Huyen Nguyen, Elisabeth Jäger, Hemisha Khatri, Lan H Chu, Rojo A Ratsimandresy, Andrea Dorfleutner and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Nature immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. An overview of human inflammasomes: Activation and regulation.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  6. Article
  7. The Roles of Interleukin-18 in Inflammation and Autoimmune Disease.Clinical reviews in allergy & immunology · 2026
    Review
  8. Diverse Scaffolds Facilitate NLRP3 Clustering and Inflammasome Formation in Response to Perturbations in Cell Homeostasis.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Pattern Recognition by NOD-Like Receptors.Advances in experimental medicine and biology · 2025
    Review
  16. Article
  17. Review
  18. Review
  19. Mechanistic insights from inflammasome structures.Nature reviews. Immunology · 2024
    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

11 authors at 2 institutions in 1 country.

Anu Gangopadhyay *Department of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.
Savita Devi *Department of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.
Shivendra Tenguria *Department of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.
Jessica CarriereDepartment of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.
Huyen NguyenDepartment of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-6999-3544
Elisabeth JägerDepartment of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0001-7342-3459
Hemisha KhatriDepartment of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.
Lan H ChuDriskill Graduate Program in Life Sciences, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Rojo A RatsimandresyDepartment of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA.
Andrea DorfleutnerDepartment of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA. andrea.dorfleutner@cshs.org.ORCID http://orcid.org/0000-0003-4406-2986
Christian StehlikDepartment of Academic Pathology, Cedars Sinai Medical Center, Los Angeles, CA, USA. christian.stehlik@csmc.edu.ORCID http://orcid.org/0000-0002-3782-2484
Cedars-Sinai Medical Center · USNorthwestern University · US

Funding

Regulation of cytosolic pattern recognition receptor signaling in macrophagesR01AI099009 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI STEHLIK, CHRISTIAN · 2013 to 2022
$4.7M
A novel mechanism for NLRP3 inflammasome activation in human macrophagesR01AI165797 · NIAID · CEDARS-SINAI MEDICAL CENTER · PI DORFLEUTNER, ANDREA, STEHLIK, CHRISTIAN · 2022 to 2025
$3.8M
A novel essential inflammasome component propagating inflammatory responsesR01AI134030 · NIAID · CEDARS-SINAI MEDICAL CENTER · PI DORFLEUTNER, ANDREA, STEHLIK, CHRISTIAN · 2019 to 2023
$3.1M
CARD-only protein regulation of cytosolic Pattern Recognition Receptor signalingR01AI140702 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DORFLEUTNER, ANDREA, STEHLIK, CHRISTIAN · 2018 to 2022
$2.9M
Molecular Regulation of Systemic InflammationR01AI120625 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DORFLEUTNER, ANDREA, STEHLIK, CHRISTIAN · 2016 to 2020
$2.0M
A Regulatory Checkpoint in the Pathogenesis of Inflammatory ArthritisR01AR064349 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI STEHLIK, CHRISTIAN · 2013 to 2017
$1.9M
NIAID NIH HHS R01 AI099009NIAID NIH HHS R01 AI120625NIAID NIH HHS R01 AI134030NIAID NIH HHS R01 AI140702NIAID NIH HHS R01 AI165797NIAMS NIH HHS R01 AR064349
6 · The paper itself

Abstract

Intracellular sensing of stress and danger signals initiates inflammatory innate immune responses by triggering inflammasome assembly, caspase-1 activation and pyroptotic cell death as well as the release of interleukin 1β (IL-1β), IL-18 and danger signals. NLRP3 broadly senses infectious patterns and sterile danger signals, resulting in the tightly coordinated and regulated assembly of the NLRP3 inflammasome, but the precise mechanisms are incompletely understood. Here, we identified NLRP11 as an essential component of the NLRP3 inflammasome in human macrophages. NLRP11 interacted with NLRP3 and ASC, and deletion of NLRP11 specifically prevented NLRP3 inflammasome activation by preventing inflammasome assembly, NLRP3 and ASC polymerization, caspase-1 activation, pyroptosis and cytokine release but did not affect other inflammasomes. Restored expression of NLRP11, but not NLRP11 lacking the PYRIN domain (PYD), restored inflammasome activation. NLRP11 was also necessary for inflammasome responses driven by NLRP3 mutations that cause cryopyrin-associated periodic syndrome (CAPS). Because NLRP11 is not expressed in mice, our observations emphasize the specific complexity of inflammasome regulation in humans.

Indexed as

InflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinAnimalsCaspase 1CaspasesHumansInterleukin-1betaLicensureMacrophagesMiceCaspase 1CaspasesInflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouse

Identifiers

PMID35624206
PMCPMC9174058
OpenAlexW4281631100

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.