Evidence map›Paper›PMID 28507543›Full record

ArticleFrontiers in immunology2017

Long-term Monocyte Dysfunction after Sepsis in Humanized Mice Is Related to Persisted Activation of Macrophage-Colony Stimulation Factor (M-CSF) and Demethylation of PU.1, and It Can Be Reversed by Blocking M-CSF

Natalia Lapko, Mateusz Zawadka, Jacek Polosak, George S Worthen, Gwenn Danet-Desnoyers, Monika Puzianowska-Kuźnicka, Krzysztof Laudanski

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 28% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Prolonged Transcriptional Consequences in Survivors of Sepsis.International journal of molecular sciences · 2021
    Article
  9. Humanized Mice as a Tool to Study Sepsis-More Than Meets the Eye.International journal of molecular sciences · 2021
    Review
  10. Review
  11. Article
  12. Article
  13. New Insights into the Immune System Using Dirty Mice.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Review
  14. Article
  15. Review
  16. Potential Pitfalls of the Humanized Mice in Modeling Sepsis.International journal of inflammation · 2018
    Review
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

7 authors at 5 institutions in 3 countries.

Natalia Lapko2nd Department of Anesthesiology and Intensive Care, Medical University of Warsaw, Warsaw, Poland.
Mateusz ZawadkaFaculty of Medicine, Ivano-Frankivsk Medical Institute, Ivano-Frankivsk, Ukraine.
Jacek PolosakDepartment of Human Epigenetics, Mossakowski Medical Research Centre, PAS, Warsaw, Poland.
George S WorthenDepartment of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Gwenn Danet-DesnoyersDepartment of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Monika Puzianowska-KuźnickaDepartment of Human Epigenetics, Mossakowski Medical Research Centre, PAS, Warsaw, Poland.
Krzysztof LaudanskiDepartment of Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, PA, USA.
Mossakowski Medical Research Institute, Polish Academy of Sciences · PLUniversity of Pennsylvania · USChildren's Hospital of Philadelphia · USIvano-Frankivsk National Medical University · UAMedical University of Warsaw · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The duration of post-sepsis long-term immune suppression is poorly understood. Here, we focused on the role of monocytes (MO) as the pivotal cells for long-term regulation of post-sepsis milieu. Lost ability of MO to adapt is seen in several acute conditions, but it is unclear for how long MO aberrancy post-sepsis can persist. Interestingly, the positive feedback loop sustaining secretion of macrophage-colony stimulation factor (M-CSF) can persist even after resolution of sepsis and significantly alters performance of MO. Here, we investigated the activation of M-CSF, and it as critical regulator of PU.1 in mice surviving 28 days after sepsis. Our primary readout was the ability of MO to differentiate into dendritic cells (DCs; MO→iDC)

Indexed as

dendritic cellsepigenetic regulationimmunosuppressionmacrophage-colony stimulation factormonocytePU.1sepsisstem cells

Identifiers

PMID28507543
PMCPMC5410640
OpenAlexW2611251242

What OpenQuestion holds

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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.