Evidence map›Paper›PMID 25887317›Full record

ReviewBMC immunology2015

Current challenges in understanding immune cell functions during septic syndromes.

Zechariah Franks, McKenzie Carlisle, Matthew T Rondina

Abstract readReview
In one paragraph

Review in BMC immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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.

Zechariah FranksProgram in Molecular Medicine, Salt Lake City, 84112, , Utah, USA. zfranks@u2m2.utah.edu.
McKenzie CarlisleProgram in Molecular Medicine, Salt Lake City, 84112, , Utah, USA. m.carlisle@u2m2.utah.edu.
Matthew T RondinaProgram in Molecular Medicine, Salt Lake City, 84112, , Utah, USA. matt.rondina@u2m2.utah.edu.

Funding

Translational Research Skills Development CoreU54HL112311 · NHLBI · UNIVERSITY OF UTAH · PI WEYRICH, ANDREW S, ZIMMERMAN, GUY A. · 2012 to 2016
$12.9M
The Effects of ART on Platelets and HIV-Associated ThrombosisR01HL126547 · NHLBI · UNIVERSITY OF UTAH · PI PLANELLES, VICENTE, RONDINA, MATTHEW THOMAS · 2014 to 2017
$3.0M
Platelet Immune Responses in Aging and InfluenzaR01AG048022 · NIA · UNIVERSITY OF UTAH · PI RONDINA, MATTHEW THOMAS · 2014 to 2018
$1.8M
Novel Platelet Functions in Sepsis and Venous ThromboembolismK23HL092161 · NHLBI · UNIVERSITY OF UTAH · PI RONDINA, MATTHEW THOMAS · 2009 to 2013
$775k
The Regulation of Inflammatory Gene Responses in AgingR03AG040631 · NIA · UNIVERSITY OF UTAH · PI RONDINA, MATTHEW THOMAS · 2011 to 2012
$149k
NHLBI NIH HHS K23 HL092161NHLBI NIH HHS K23HL092161NHLBI NIH HHS R01 HL126547NHLBI NIH HHS U54 HL112311NHLBI NIH HHS U54HL112311NIA NIH HHS R01 AG048022NIA NIH HHS R01AG048022NIA NIH HHS R03 AG040631NIA NIH HHS R03AG040631
6 · The paper itself

Abstract

backgroundSepsis is a dynamic infectious disease syndrome characterized by dysregulated inflammatory responses.

resultsDespite decades of research, improvements in the treatment of sepsis have been modest. These limited advances are likely due, in part, to multiple factors, including substantial heterogeneity in septic syndromes, significant knowledge gaps in our understanding of how immune cells function in sepsis, and limitations in animal models that accurately recapitulate the human septic milieu. The goal of this brief review is to describe current challenges in understanding immune cell functions during sepsis. We also provide a framework to guide scientists and clinicians in research and patient care as they strive to better understand dysregulated cell responses during sepsis.

conclusionsAdditional, well-designed translational studies in sepsis are critical for enhancing our understanding of the role of immune cells in sepsis.

Indexed as

Immunity, CellularAnimalsDisease Models, AnimalHumansInflammationPatient CareSystemic Inflammatory Response SyndromeTranslational Research, Biomedical

Identifiers

PMID25887317
PMCPMC4374283

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.