Evidence map›Paper›PMID 31028123›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2019

Twist1 and Twist2 Induce Human Macrophage Memory upon Chronic Innate Receptor Treatment by HDAC-Mediated Deacetylation of Cytokine Promoters.

Rui Sun, Matija Hedl, Clara Abraham

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Memory Macrophages.International journal of molecular sciences · 2022
    Review
  6. Article
  7. Review
  8. Innate Immune Memory and the Host Response to Infection.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. Twist1: A Double-Edged Sword in Kidney Diseases.Kidney diseases (Basel, Switzerland) · 2020
    Review
  13. Innate Immune Memory in Macrophages.Newborn (Clarksville, Md.)
    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

3 authors at 1 institution in 1 country.

Rui SunDepartment of Internal Medicine, Yale University, New Haven, CT 06510.ORCID 0000-0003-4054-1365
Matija HedlDepartment of Internal Medicine, Yale University, New Haven, CT 06510.
Clara AbrahamDepartment of Internal Medicine, Yale University, New Haven, CT 06510 clara.abraham@yale.edu.
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 Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI YASUKO IWAKIRI · 1986 to 2026
$31.1M
Yale University Inflammatory Bowel Disease Genetics Research CenterU01DK062422 · NIDDK · YALE UNIVERSITY · PI Ling-shiang Chuang · 2002 to 2026
$10.8M
Functional outcomes of inflammatory bowel disease associated variantsR01DK099097 · NIDDK · YALE UNIVERSITY · PI CLARA ABRAHAM · 2013 to 2026
$7.0M
Integrative Genomic Analyses of Macrophages in Crohns DiseaseR01DK106593 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CHO, JUDY H. · 2016 to 2020
$3.8M
Mechanisms Regulating Innate Immune ResponsesR01AI120369 · NIAID · YALE UNIVERSITY · PI ABRAHAM, CLARA · 2016 to 2020
$2.0M
Mechanisms of Chronic Nod2-mediated Effects in Human MacrophagesR01DK077905 · NIDDK · YALE UNIVERSITY · PI ABRAHAM, CLARA · 2008 to 2012
$1.7M
NCATS NIH HHS UL1 TR001863NIAID NIH HHS R01 AI120369NIDDK NIH HHS P30 DK034989NIDDK NIH HHS R01 DK077905NIDDK NIH HHS R01 DK099097NIDDK NIH HHS R01 DK106593NIDDK NIH HHS U01 DK062422
6 · The paper itself

Abstract

Intestinal tissues are continuously exposed to microbial products that stimulate pattern-recognition receptors (PRRs). Ongoing PRR stimulation can confer epigenetic changes in macrophages, which can then regulate subsequent immune outcomes and adaptation to the local environment. Mechanisms leading to these changes are incompletely understood. We found that short-term stimulation of the PRR NOD2 in primary human monocyte-derived macrophages resulted in increased H3 and H4 acetylation of cytokine promoters, consistent with the increased cytokine secretion observed. However, with prolonged NOD2 stimulation, both the acetylation and cytokine secretion were dramatically decreased. Chronic NOD2 stimulation upregulated the transcription factors Twist1 and Twist2, which bound to the promoters of the histone deacetylases

Indexed as

AcetylationAnimalsCells, CulturedCytokinesGene Expression RegulationHistone Deacetylase 1Histone Deacetylase 3Histone DeacetylasesHistonesHumansMacrophagesMiceMice, Inbred C57BLMonocytesPromoter Regions, GeneticProtein BindingCytokinesHistone Deacetylase 1Histone Deacetylase 3Histone DeacetylasesHistonesReceptors, Pattern RecognitionTwist-Related Protein 1Twist-Related Protein 2

Identifiers

PMID31028123
PMCPMC6615459
OpenAlexW2942098717

What OpenQuestion 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 OpenQuestion graph.