Evidence map›Paper›PMID 33482101›Full record

ArticleStem cell reports2021

Murine Myeloid Progenitors Attenuate Immune Dysfunction Induced by Hemorrhagic Shock.

Joshua T Cohen, Michael Danise, Jason T Machan, Runping Zhao, Craig T Lefort

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Bi-fluorescentFrontiers in immunology · 2023
    Article
  6. Review
  7. Article
  8. Article
  9. 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

5 authors at 1 institution in 1 country.

Joshua T CohenDivision of Surgical Research, Department of Surgery, Rhode Island Hospital, 593 Eddy Street, Providence, RI 02903, USA.
Michael DaniseDivision of Surgical Research, Department of Surgery, Rhode Island Hospital, 593 Eddy Street, Providence, RI 02903, USA.
Jason T MachanLifespan Biostatistics Core, Rhode Island Hospital, Providence, RI 02903, USA.
Runping ZhaoDivision of Surgical Research, Department of Surgery, Rhode Island Hospital, 593 Eddy Street, Providence, RI 02903, USA.
Craig T LefortDivision of Surgical Research, Department of Surgery, Rhode Island Hospital, 593 Eddy Street, Providence, RI 02903, USA. Electronic address: craig_lefort@brown.edu.
Providence College · US

Funding

Selective Modulation of Neutrophils in Critical IllnessR35GM124911 · NIGMS · RHODE ISLAND HOSPITAL · PI CRAIG THOMAS LEFORT · 2017 to 2026
$3.8M
Trauma and Inflammation Research TrainingT32GM065085 · NIGMS · RHODE ISLAND HOSPITAL · PI Alfred Ayala · 2004 to 2026
$3.2M
NIGMS NIH HHS R35 GM124911NIGMS NIH HHS T32 GM065085
6 · The paper itself

Abstract

Hemorrhagic shock induces an aberrant immune response characterized by simultaneous induction of a proinflammatory state and impaired host defenses. The objective of this study was to evaluate the impact of conditionally immortalized neutrophil progenitors (NPs) on this aberrant immune response. We employed a mouse model of hemorrhagic shock, followed by the adoptive transfer of NPs and subsequent inoculation of Staphylococcus aureus to induce pneumonia. We observed that transplant of NPs decreases the proportion of host neutrophils that express programmed death ligand 1 and intercellular adhesion molecule 1 in the context of prior hemorrhage. Following hemorrhage, NP transplant decreased proinflammatory cytokines in the lungs, increased neutrophil migration into the airspaces, and enhanced bacterial clearance. Further, hemorrhagic shock improved NP engraftment in the bone marrow. These results suggest that NPs hold the potential for use as a cellular therapy in the treatment and prevention of secondary infection following hemorrhagic shock.

Indexed as

AnimalsB7-H1 AntigenBone MarrowCell- and Tissue-Based TherapyCell LineCell MovementCytokinesDisease Models, AnimalImmunityIntercellular Adhesion Molecule-1LungMiceMice, Inbred C57BLMyeloid Progenitor CellsNeutrophilsPneumoniaB7-H1 AntigenCytokinesIntercellular Adhesion Molecule-1bone marrow engraftmentcell therapyhemorrhagic shockICAM-1myeloid progenitorsneutrophil primingPD-L1pneumoniaStaphylococcus aureus

Identifiers

PMID33482101
PMCPMC7878835
OpenAlexW3122202871

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.