Evidence map›Paper›PMID 34269788›Full record

ArticleThe Journal of experimental medicine2021

CD16+CD163+ monocytes traffic to sites of inflammation during necrotizing enterocolitis in premature infants.

Oluwabunmi O Olaloye, Peng Liu, Jessica M Toothaker, Blake T McCourt, Collin C McCourt, Jenny Xiao, Erica Prochaska, Spenser Shaffer, Lael Werner, UPMC NICU Faculty and 11 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 54 citations in OpenAlex.

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  16. Single-Cell Imaging Maps Inflammatory Cell Subsets to Pulmonary Arterial Hypertension Vasculopathy.American journal of respiratory and critical care medicine · 2024
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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

21 authors at 8 institutions in 2 countries.

Oluwabunmi O Olaloye *Department of Pediatrics, Yale Medical School, New Haven, CT.ORCID 0000-0002-9217-3333
Peng Liu *Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA.ORCID 0000-0003-4012-3884
Jessica M ToothakerDepartment of Immunology, University of Pittsburgh, Pittsburgh, PA.ORCID 0000-0002-4535-5337
Blake T McCourtDepartment of Pediatrics, Yale Medical School, New Haven, CT.ORCID 0000-0002-1488-2572
Collin C McCourtDepartment of Pediatrics, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, Pittsburgh, PA.ORCID 0000-0002-8735-1529
Jenny XiaoDepartment of Biology, University of Pittsburgh, Pittsburgh, PA.ORCID 0000-0001-8804-2675
Erica ProchaskaDivision of Infectious Diseases, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD.ORCID 0000-0003-3655-1384
Spenser ShafferDivision of Newborn Medicine, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, Pittsburgh, PA.ORCID 0000-0003-1243-3869
Lael WernerInstitute of Gastroenterology, Nutrition and Liver Disease, Schneider Children's Medical Center of Israel, Petah Tiqwa, Israel.ORCID 0000-0002-3590-2798
UPMC NICU Faculty
UPMC Pediatric Surgery Faculty
Jordan GringauzDepartment of Medicine, Boston Children's Hospital, Boston, MA.ORCID 0000-0002-4565-5188
Misty GoodDepartment of Pediatrics, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0002-0264-5721
Jeffrey D GoldsmithDepartment of Pathology, Boston Children's Hospital, Boston, MA.ORCID 0000-0003-4566-1307
Xiaojing AnDepartment of Medicine, University of Pittsburgh Medical Center Montefiore Hospital, Pittsburgh, PA.ORCID 0000-0002-1962-8995
Fujing WangDepartment of Medicine, University of Pittsburgh Medical Center Montefiore Hospital, Pittsburgh, PA.ORCID 0000-0002-6381-5309
Scott B SnapperDivision of Gastroenterology, Hepatology and Nutrition, Boston Children's Hospital, Boston, MA.ORCID 0000-0003-0267-4247
Dror ShouvalInstitute of Gastroenterology, Nutrition and Liver Disease, Schneider Children's Medical Center of Israel, Petah Tiqwa, Israel.ORCID 0000-0001-5980-2954
Kong ChenDepartment of Medicine, University of Pittsburgh Medical Center Montefiore Hospital, Pittsburgh, PA.ORCID 0000-0001-6980-5454
George TsengDepartment of Biostatistics, University of Pittsburgh, Pittsburgh, PA.ORCID 0000-0002-5447-1014
Liza KonnikovaDepartment of Pediatrics, Yale Medical School, New Haven, CT.ORCID 0000-0003-4804-5497
University of Pittsburgh · USBoston Children's Hospital · USUniversity of Pittsburgh Medical Center · USChildren's Hospital of Pittsburgh · USTel Aviv University · ILYale University · USJohns Hopkins University · USWashington University in St. Louis · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
STRUCTURE-FUNCTION RELATIONSHIPS IN THE ALIMENTARY TRACTP30DK034854 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WAYNE I LENCER · 1986 to 2026
$32.4M
Peripheral Immune Development in Premature Infants with and without NECR21HD102565 · NICHD · YALE UNIVERSITY · PI KONNIKOVA, LIZA, TSENG, GEORGE C. · 2020 to 2021
$456k
NCATS NIH HHS UL1 TR001863NICHD NIH HHS 1R21HD102565-01A1NICHD NIH HHS R21 HD102565NIDDK NIH HHS P30 DK034854
6 · The paper itself

Abstract

Necrotizing enterocolitis (NEC) is a severe gastrointestinal complication of prematurity. Using suspension and imaging mass cytometry coupled with single-cell RNA sequencing, we demonstrate severe inflammation in patients with NEC. NEC mucosa could be subtyped by an influx of three distinct neutrophil phenotypes (immature, newly emigrated, and aged). Furthermore, CD16+CD163+ monocytes/Mϕ, correlated with newly emigrated neutrophils, were specifically enriched in NEC mucosa, found adjacent to the blood vessels, and increased in circulation of infants with surgical NEC, suggesting trafficking from the periphery to areas of inflammation. NEC-specific monocytes/Mϕ transcribed inflammatory genes, including TREM1, IL1A, IL1B, and calprotectin, and neutrophil recruitment genes IL8, CXCL1, CXCL2, CXCL5 and had enrichment of gene sets in pathways involved in chemotaxis, migration, phagocytosis, and reactive oxygen species generation. In summary, we identify a novel subtype of inflammatory monocytes/Mϕ associated with NEC that should be further evaluated as a potential biomarker of surgical NEC and a target for the development of NEC-specific therapeutics.

Indexed as

Antigens, CDAntigens, Differentiation, MyelomonocyticReceptors, Cell SurfaceReceptors, IgGBlood VesselsCase-Control StudiesCD163 AntigenChemotaxisEnterocolitis, NecrotizingGastric MucosaGPI-Linked ProteinsHumansInfantInfant, NewbornIntestine, SmallMonocytesAntigens, CDAntigens, Differentiation, MyelomonocyticCD163 AntigenFCGR3B protein, humanGPI-Linked ProteinsReactive Oxygen SpeciesReceptors, Cell SurfaceReceptors, IgG

Identifiers

PMID34269788
PMCPMC8289692
OpenAlexW3180002942

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.