Evidence map›Paper›PMID 28611952›Full record

ReviewFrontiers in cellular and infection microbiology2017

Multiple Phenotypic Changes Define Neutrophil Priming.

Irina Miralda, Silvia M Uriarte, Kenneth R McLeish

Abstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing 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

115 citing papers in PubMed.

  1. Trial
  2. International journal of molecular sciences · 2026
    Article
  3. Myeloid cell reprogramming drives enhanced defense againstbioRxiv : the preprint server for biology · 2026
    Article
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  8. Review
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  16. Review
  17. Review
  18. Article
  19. Article
  20. The roles of neutrophils in cardiovascular diseases.Frontiers in cardiovascular medicine · 2025
    Review

55 more citing papers are in PubMed but not listed here.

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.

Irina MiraldaDepartment of Microbiology, University of Louisville School of MedicineLouisville, KY, United States.
Silvia M UriarteDepartment of Microbiology, University of Louisville School of MedicineLouisville, KY, United States.
Kenneth R McLeishDepartment of Medicine, University of Louisville School of MedicineLouisville, KY, United States.

Funding

Filifactor alocis interactions with neutrophilsR01DE024509 · NIDCR · UNIVERSITY OF LOUISVILLE · PI URIARTE, SILVIA M · 2014 to 2023
$4.2M
BLRD VA I01 BX001838NIDCR NIH HHS R01 DE024509
6 · The paper itself

Abstract

Exposure to pro-inflammatory cytokines, chemokines, mitochondrial contents, and bacterial and viral products induces neutrophils to transition from a basal state into a primed one, which is currently defined as an enhanced response to activating stimuli. Although, typically associated with enhanced generation of reactive oxygen species (ROS) by the NADPH oxidase, primed neutrophils show enhanced responsiveness of exocytosis, NET formation, and chemotaxis. Phenotypic changes associated with priming also include activation of a subset of functions, including adhesion, transcription, metabolism, and rate of apoptosis. This review summarizes the breadth of phenotypic changes associated with priming and reviews current knowledge of the molecular mechanisms behind those changes. We conclude that the current definition of priming is too restrictive. Priming represents a combination of enhanced responsiveness and activated functions that regulate both adaptive and innate immune responses.

Indexed as

PhenotypeApoptosisCell AdhesionChemokinesChemotaxisCytokinesExocytosisExtracellular TrapsExtracellular VesiclesHumansImmunity, InnateLipid MetabolismNADPH OxidasesNeutrophilsPhagocytosisReactive Oxygen SpeciesChemokinesCytokinesNADPH OxidasesReactive Oxygen Speciesapoptosischemotaxiscytokinesexocytosisneutrophilsphagocytosisprimingrespiratory burst

Identifiers

PMID28611952
PMCPMC5447094

What OpenQuestion holds

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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.