Evidence map›Paper›PMID 35256513›Full record

ArticleLife science alliance2022

LRR-protein RNH1 dampens the inflammasome activation and is associated with COVID-19 severity.

Giuseppe Bombaci, Mayuresh Anant Sarangdhar, Nicola Andina, Aubry Tardivel, Eric Chi-Wang Yu, Gillian M Mackie, Matthew Pugh, Vedat Burak Ozan, Yara Banz, Thibaud Spinetti and 10 more

Open access · goldAbstract read
In one paragraph

Article in Life science alliance, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

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  9. Frontiers in immunology · 2023
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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

20 authors at 4 institutions in 2 countries.

Giuseppe BombaciDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID 0000-0002-0752-4769
Mayuresh Anant SarangdharDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID 0000-0001-5653-8991
Nicola AndinaDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID 0000-0002-2924-6763
Aubry TardivelDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Eric Chi-Wang YuDepartment of Biochemistry, University of Lausanne, Lausanne, Switzerland.ORCID 0000-0001-7026-7008
Gillian M MackieInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.ORCID 0000-0001-7758-6570
Matthew PughInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.ORCID 0000-0002-6324-661X
Vedat Burak OzanDepartment for BioMedical Research, University of Bern, Bern, Switzerland.ORCID 0000-0002-6813-6348
Yara BanzInstitute of Pathology, University of Bern, Bern, Switzerland.
Thibaud SpinettiDepartment of Intensive Care Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID 0000-0001-8057-3746
Cedric HirzelDepartment of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID 0000-0002-7870-912X
Esther YoudSchool of Medicine, Dentistry and Nursing, Forensic Medicine and Science. University of Glasgow, Scotland, UK.
Joerg C SchefoldDepartment of Intensive Care Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.ORCID 0000-0001-9162-5724
Graham TaylorInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.ORCID 0000-0002-4807-2797
Amiq GazdharDepartment for BioMedical Research, University of Bern, Bern, Switzerland.
Nicolas BonadiesDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Anne Angelillo-ScherrerDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Pascal SchneiderDepartment of Biochemistry, University of Lausanne, Lausanne, Switzerland.ORCID 0000-0003-0677-9409
Kendle M MaslowskiInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.ORCID 0000-0003-1995-5424
Ramanjaneyulu AllamDepartment of Hematology and Central Hematology Laboratory, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland allam.ramanjaneyulu@dbmr.unibe.ch.ORCID 0000-0002-2789-3596
University of Bern · CHUniversity of Birmingham · GBUniversity of Lausanne · CHUniversity of Glasgow · GB

Funding

Medical Research Council MR/T001755/1
6 · The paper itself

Abstract

Inflammasomes are cytosolic innate immune sensors of pathogen infection and cellular damage that induce caspase-1-mediated inflammation upon activation. Although inflammation is protective, uncontrolled excessive inflammation can cause inflammatory diseases and can be detrimental, such as in coronavirus disease (COVID-19). However, the underlying mechanisms that control inflammasome activation are incompletely understood. Here we report that the leucine-rich repeat (LRR) protein ribonuclease inhibitor (RNH1), which shares homology with LRRs of NLRP (nucleotide-binding oligomerization domain, leucine-rich repeat, and pyrin domain containing) proteins, attenuates inflammasome activation. Deletion of RNH1 in macrophages increases interleukin (IL)-1β production and caspase-1 activation in response to inflammasome stimulation. Mechanistically, RNH1 decreases pro-IL-1β expression and induces proteasome-mediated caspase-1 degradation. Corroborating this, mouse models of monosodium urate (MSU)-induced peritonitis and lipopolysaccharide (LPS)-induced endotoxemia, which are dependent on caspase-1, respectively, show increased neutrophil infiltration and lethality in

Indexed as

AnimalsCarrier ProteinsCaspase 1COVID-19HumansInflammasomesLeucine-Rich Repeat ProteinsMaleMiceMice, Inbred C57BLMice, KnockoutNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinPatient AcuityProteasome Endopeptidase ComplexCarrier ProteinsCaspase 1InflammasomesLeucine-Rich Repeat ProteinsNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanProteasome Endopeptidase ComplexRNH1 protein, human

Identifiers

PMID35256513
PMCPMC8922048
OpenAlexW4220994709

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.