Evidence map›Paper›PMID 27630164›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Transcriptional Repression of IFN Regulatory Factor 7 by MYC Is Critical for Type I IFN Production in Human Plasmacytoid Dendritic Cells.

Tae Whan Kim, Seunghee Hong, Yin Lin, Elise Murat, HyeMee Joo, Taeil Kim, Virginia Pascual, Yong-Jun Liu

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Human CD34Frontiers in immunology · 2024
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  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Type I Interferon Production of Plasmacytoid Dendritic Cells under Control.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
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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

8 authors at 1 institution in 1 country.

Tae Whan KimBaylor Institute for Immunology Research, Dallas, TX 75204; and Yong-Jun.liu@sanofi.com TaeWhan.Kim@BSWHealth.org.
Seunghee HongBaylor Institute for Immunology Research, Dallas, TX 75204; and.
Yin LinBaylor Institute for Immunology Research, Dallas, TX 75204; and.
Elise MuratBaylor Institute for Immunology Research, Dallas, TX 75204; and.ORCID 0000-0003-2156-334X
HyeMee JooBaylor Institute for Immunology Research, Dallas, TX 75204; and.
Taeil KimSanofi, Cambridge, MA 02139.
Virginia PascualBaylor Institute for Immunology Research, Dallas, TX 75204; and.
Yong-Jun LiuBaylor Institute for Immunology Research, Dallas, TX 75204; and Yong-Jun.liu@sanofi.com TaeWhan.Kim@BSWHealth.org.
Baylor University · US

Funding

Understanding the early and late endosomal TLR9-mediated responses to viral DNA.R01AI097348 · NIAID · BAYLOR RESEARCH INSTITUTE · PI LIU, YONG-JUN · 2012 to 2014
$1.2M
NIAID NIH HHS R01 AI097348
6 · The paper itself

Abstract

Type I IFNs are crucial mediators of human innate and adaptive immunity and are massively produced from plasmacytoid dendritic cells (pDCs). IFN regulatory factor (IRF)7 is a critical regulator of type I IFN production when pathogens are detected by TLR 7/9 in pDC. However, hyperactivation of pDC can cause life-threatening autoimmune diseases. To avoid the deleterious effects of aberrant pDC activation, tight regulation of IRF7 is required. Nonetheless, the detailed mechanisms of how IRF7 transcription is regulated in pDC are still elusive. MYC is a well-known highly pleiotropic transcription factor; however, the role of MYC in pDC function is not well defined yet. To identify the role of transcription factor MYC in human pDC, we employed a knockdown technique using human pDC cell line, GEN2.2. When we knocked down MYC in the pDC cell line, production of IFN-stimulated genes was dramatically increased and was further enhanced by the TLR9 agonist CpGB. Interestingly, MYC is shown to be recruited to the IRF7 promoter region through interaction with nuclear receptor corepressor 2/histone deacetylase 3 for its repression. In addition, activation of TLR9-mediated NF-κB and MAPK and nuclear translocation of IRF7 were greatly enhanced by MYC depletion. Pharmaceutical inhibition of MYC recovered IRF7 expression, further confirming the negative role of MYC in the antiviral response by pDC. Therefore, our results identify the novel immunomodulatory role of MYC in human pDC and may add to our understanding of aberrant pDC function in cancer and autoimmune disease.

Indexed as

Transcription, GeneticCells, CulturedDendritic CellsHumansInterferon Regulatory Factor-7Interferon Type IProto-Oncogene Proteins c-mycInterferon Regulatory Factor-7Interferon Type IProto-Oncogene Proteins c-myc

Identifiers

PMID27630164
PMCPMC5101139
OpenAlexW2520792777

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.