Evidence map›Paper›PMID 26417909›Full record

ArticleAmerican journal of respiratory and critical care medicine2016

Inhibition of Neutrophil Extracellular Trap Formation after Stem Cell Transplant by Prostaglandin E2.

Racquel Domingo-Gonzalez, Giovanny J Martínez-Colón, Alana J Smith, Carolyne K Smith, Megan N Ballinger, Meng Xia, Susan Murray, Mariana J Kaplan, Gregory A Yanik, Bethany B Moore

Abstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 2 pooled it
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

54 citing papers in PubMed, 2 syntheses or guidelines pooled it, 80 citations in OpenAlex.

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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

10 authors at 7 institutions in 2 countries.

Racquel Domingo-Gonzalez1 Immunology Graduate Program.
Giovanny J Martínez-Colón1 Immunology Graduate Program.
Alana J Smith2 Summer Undergraduate Research Program.
Carolyne K Smith1 Immunology Graduate Program.
Megan N Ballinger4 Pulmonary, Allergy, Critical Care and Sleep Division, Department of Internal Medicine, The Ohio State University, Columbus, Ohio.
Meng Xia5 Biostatistics Department, School of Public Health.
Susan Murray5 Biostatistics Department, School of Public Health.ORCID http://orcid.org/0000-0003-4387-7673
Mariana J Kaplan3 Systemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland; and.
Gregory A Yanik6 Department of Pediatrics, Division of Hematology-Oncology, Medical School.
Bethany B Moore7 Pulmonary and Critical Care Medicine Division, Department of Internal Medicine, and.ORCID http://orcid.org/0000-0003-3051-745X
Cancer Research And Biostatistics · USInstitute of Immunology · HRNational Institutes of Health · USMaryland Oncology Hematology · USResearch Experiences for Undergraduates · USThe Ohio State University · USUniversity of Michigan · US

Funding

Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
Systemic AutoimmunityZIAAR041199 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI KAPLAN, MARIANA · 2014 to 2025
$32.5M
RESEARCH TRAINING IN EXPERIMENTAL IMMUNOPATHOLOGYT32AI007413 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Bethany B. Moore · 1993 to 2026
$9.8M
University of Michigan Postbaccalaureate Research Education Program (UM PREP)R25GM086262 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ALLEN, BENJAMIN · 2009 to 2024
$6.1M
miR-29b and autophagy regulate alveolar macrophage function post-BMTR01AI117229 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOORE, BETHANY B. · 2015 to 2019
$2.2M
Periostin Regulation of Lung FibrosisR01HL115618 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOORE, BETHANY B. · 2013 to 2016
$1.6M
Promoting Diversity of Future ScientistsR25HL108842 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Susan V Brooks · 2011 to 2026
$1.3M
HSCT-induced changes that impair lung innate immunityR56AI065543 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOORE, BETHANY B. · 2012 to 2012
$363k
NCATS NIH HHS UL1 TR000433NCATS NIH HHS UL1TR000433NHLBI NIH HHS HL115618NHLBI NIH HHS R01 HL115618NHLBI NIH HHS R25 HL108842NIAID NIH HHS AI117229NIAID NIH HHS R01 AI117229NIAID NIH HHS R56 AI065543NIAID NIH HHS R56AI065543NIAID NIH HHS T32 AI007413NIAID NIH HHS T32AI007413NIGMS NIH HHS R25 GM086262
6 · The paper itself

Abstract

rationaleAutologous and allogeneic hematopoietic stem cell transplant (HSCT) patients are susceptible to pulmonary infections, including bacterial pathogens, even after hematopoietic reconstitution. We previously reported that murine bone marrow transplant (BMT) neutrophils overexpress cyclooxygenase-2, overproduce prostaglandin E2 (PGE2), and exhibit defective intracellular bacterial killing. Neutrophil extracellular traps (NETs) are DNA structures that capture and kill extracellular bacteria and other pathogens.

objectivesTo determine whether NETosis was defective after transplant and if so, whether this was regulated by PGE2 signaling.

methodsNeutrophils isolated from mice and humans (both control and HSCT subjects) were analyzed for NETosis in response to various stimuli in the presence or absence of PGE2 signaling modifiers. MEASUREMENTS AND MAIN

resultsNETs were visualized by immunofluorescence or quantified by Sytox Green fluorescence. Treatment of BMT or HSCT neutrophils with phorbol 12-myristate 13-acetate or rapamycin resulted in reduced NET formation relative to control cells. NET formation after BMT was rescued both in vitro and in vivo with cyclooxygenase inhibitors. Additionally, the EP2 receptor antagonist (PF-04418948) or the EP4 antagonist (AE3-208) restored NET formation in neutrophils isolated from BMT mice or HSCT patients. Exogenous PGE2 treatment limited NETosis of neutrophils collected from normal human volunteers and naive mice in an exchange protein activated by cAMP- and protein kinase A-dependent manner.

conclusionsOur results suggest blockade of the PGE2-EP2 or EP4 signaling pathway restores NETosis after transplantation. Furthermore, these data provide the first description of a physiologic inhibitor of NETosis.

Indexed as

AdultAgedAnimalsDinoprostoneExtracellular TrapsFemaleHematopoietic Stem Cell TransplantationHumansMiceMice, Inbred BALB CMiddle AgedYoung AdultDinoprostonebacteriagranulocyteNETosisprostaglandintransplant

Identifiers

PMID26417909
PMCPMC4731709
OpenAlexW2120418701

What OpenQuestion holds

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Registered trials

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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.