Evidence map›Paper›PMID 36973360›Full record

ReviewNature reviews. Immunology2023

The NLR gene family: from discovery to present day.

Wei-Chun Chou, Sushmita Jha, Michael W Linhoff, Jenny P-Y Ting

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 137 papers.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed
28.8field-weighted citation impact, top 1% 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

137 citing papers in PubMed, 187 citations in OpenAlex.

  1. Article
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  7. Protein kinase F regulates the virulence ofInfection and immunity · 2026
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77 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Wei-Chun Chou *Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Sushmita Jha *Department of Bioscience and Bioengineering, Indian Institute of Technology Jodhpur, Jodhpur, India.
Michael W Linhoff *Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. michael_linhoff@med.unc.edu.
Jenny P-Y TingLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA. jenny_ting@med.unc.edu.ORCID 0000-0002-7846-0395
University of North Carolina at Chapel Hill · USIndian Institute of Technology Jodhpur · IN

Funding

Somatostatin analogues as countermeasures against intestinal radiation toxicityU19AI067798 · NIAID · DUKE UNIVERSITY · PI CHAO, NELSON J. · 2005 to 2024
$82.1M
Role of IL-10 in APC Regulation of Protective vs. Pathogenic T Cell Responses toP01DK094779 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SHEIKH, SHEHZAD Z. · 2013 to 2023
$17.9M
Intracellular Innate Immune Receptors in Cancer Suppression and ImmunotherapyR35CA232109 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TING, JENNY P · 2019 to 2025
$6.4M
Molecular and Functional Analysis of NLR Family MembersR01AI029564 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Jenny P Ting · 1991 to 2026
$6.0M
Micro-Particle Delivery of a Potent Intracellular Adjuvant for a Universal Flu VaccineR01AI141333 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BACHELDER, ERIC, TING, JENNY P · 2019 to 2023
$5.9M
Plexin-A1: Regulation by CIITA and Immunologic FunctionR37AI029564 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TING, JENNY P · 2008 to 2017
$3.8M
Role and Mitigation of Inflammasomes and Inflammation During COVID-19R01AI158314 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Beverly H Koller, Jenny P Ting · 2022 to 2026
$3.0M
Humanized mouse models for arsenic toxicologyR01ES032643 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOLLER, BEVERLY H, STYBLO, MIROSLAV · 2021 to 2025
$2.1M
Role and Mitigation of Inflammasomes and Inflammation During COVID-19R56AI158314 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOLLER, BEVERLY H, TING, JENNY P · 2021 to 2021
$768k
Plexin-A1: Regulation by CIITA and immunologic functionR56AI029564 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI TING, JENNY P.Y. · 2007 to 2007
$363k
NCI NIH HHS R35 CA232109NIAID NIH HHS R01 AI029564NIAID NIH HHS R01 AI141333NIAID NIH HHS R01 AI158314NIAID NIH HHS R37 AI029564NIAID NIH HHS R56 AI029564NIAID NIH HHS R56 AI158314NIAID NIH HHS U19 AI067798NIDDK NIH HHS P01 DK094779NIEHS NIH HHS R01 ES032643
6 · The paper itself

Abstract

The mammalian NLR gene family was first reported over 20 years ago, although several genes that were later grouped into the family were already known at that time. Although it is widely known that NLRs include inflammasome receptors and/or sensors that promote the maturation of caspase 1, IL-1β, IL-18 and gasdermin D to drive inflammation and cell death, the other functions of NLR family members are less well appreciated by the scientific community. Examples include MHC class II transactivator (CIITA), a master transcriptional activator of MHC class II genes, which was the first mammalian NBD-LRR-containing protein to be identified, and NLRC5, which regulates the expression of MHC class I genes. Other NLRs govern key inflammatory signalling pathways or interferon responses, and several NLR family members serve as negative regulators of innate immune responses. Multiple NLRs regulate the balance of cell death, cell survival, autophagy, mitophagy and even cellular metabolism. Perhaps the least discussed group of NLRs are those with functions in the mammalian reproductive system. The focus of this Review is to provide a synopsis of the NLR family, including both the intensively studied and the underappreciated members. We focus on the function, structure and disease relevance of NLRs and highlight issues that have received less attention in the NLR field. We hope this may serve as an impetus for future research on the conventional and non-conventional roles of NLRs within and beyond the immune system.

Indexed as

Gene Expression RegulationIntracellular Signaling Peptides and ProteinsAnimalsGenes, MHC Class IHumansImmunity, InnateInflammasomesMammalsInflammasomesIntracellular Signaling Peptides and ProteinsNLRC5 protein, human

Identifiers

PMID36973360
PMCPMC11171412
OpenAlexW4360991476

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.