Evidence map›Paper›PMID 36911699›Full record

ArticleFrontiers in immunology2023

NLRP6 deficiency expands a novel CD103

James A Pearson, Jian Peng, Juan Huang, Xiaoqing Yu, Ningwen Tai, Youjia Hu, Sha Sha, Richard A Flavell, Hongyu Zhao, F Susan Wong and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

11 authors at 1 institution in 2 countries.

James A PearsonSection of Endocrinology, Internal Medicine, School of Medicine, Yale University, New Haven, CT, United States.
Jian PengSection of Endocrinology, Internal Medicine, School of Medicine, Yale University, New Haven, CT, United States.
Juan HuangSection of Endocrinology, Internal Medicine, School of Medicine, Yale University, New Haven, CT, United States.
Xiaoqing YuDepartment of Bioinformatics & Data Science, School of Public Health, Yale University, New Haven, CT, United States.
Ningwen TaiSection of Endocrinology, Internal Medicine, School of Medicine, Yale University, New Haven, CT, United States.
Youjia HuSection of Endocrinology, Internal Medicine, School of Medicine, Yale University, New Haven, CT, United States.
Sha ShaSection of Endocrinology, Internal Medicine, School of Medicine, Yale University, New Haven, CT, United States.
Richard A FlavellDepartment of Immunobiology, School of Medicine, Yale University, New Haven, CT, United States.
Hongyu ZhaoDepartment of Bioinformatics & Data Science, School of Public Health, Yale University, New Haven, CT, United States.
F Susan WongDepartment of Bioinformatics & Data Science, School of Public Health, Yale University, New Haven, CT, United States.
Li WenSection of Endocrinology, Internal Medicine, School of Medicine, Yale University, New Haven, CT, United States.
Yale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Kevan C Herold, GERALD I SHULMAN · 1993 to 2026
$44.0M
Antibody and gut bacteria in obesity and T2DR01DK126809 · NIDDK · YALE UNIVERSITY · PI WEN, LI · 2021 to 2024
$1.8M
Identifying immunoregulatory gut bacteria in type 1 diabetes and autoimmunityR01DK130318 · NIDDK · YALE UNIVERSITY · PI WEN, LI · 2022 to 2025
$1.6M
Investigating the early development of the immune system and islet autoimmunity later in lifeR01HD097808 · NICHD · YALE UNIVERSITY · PI WEN, LI · 2019 to 2021
$1.3M
Medical Research Council MR/T010525/1NCATS NIH HHS UL1 TR001863NICHD NIH HHS R01 HD097808NIDDK NIH HHS P30 DK045735NIDDK NIH HHS R01 DK126809NIDDK NIH HHS R01 DK130318
6 · The paper itself

Abstract

Introduction: Gut microbiota have been linked to modulating susceptibility to Type 1 diabetes; however, there are many ways in which the microbiota interact with host cells, including through microbial ligand binding to intracellular inflammasomes (large multi-subunit proteins) to initiate immune responses. NLRP6, a microbe-recognizing inflammasome protein, is highly expressed by intestinal epithelial cells and can alter susceptibility to cancer, obesity and Crohn's disease; however, the role of NLRP6 in modulating susceptibility to autoimmune diabetes, was previously unknown. Methods: We generated NLRP6-deficient Non-obese diabetic (NOD) mice to study the effect of NLRP6-deficiency on the immune cells and susceptibility to Type 1 diabetes development. Results: NLRP6-deficient mice exhibited an expansion of CD103 Discussion: Together, our data indicate that NLRP6 deficiency promotes expansion and maintenance of a novel TGF -dependent CD103

Indexed as

Diabetes Mellitus, Type 1Interleukin-10AnimalsImmune ToleranceInflammasomesLipopolysaccharidesMiceMice, Inbred NODReceptors, Cell SurfaceInflammasomesInterleukin-10LipopolysaccharidesNod-like receptor pyrin domain-containing protein 6, mouseReceptors, Cell SurfaceinflammasomemicrobiomeNLRP6non-obese diabetic (NOD) micetype 1 diabetes (T1D)

Identifiers

PMID36911699
PMCPMC9995752
OpenAlexW4321599675

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.