Evidence map›Paper›PMID 28993515›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Nonclassical Monocytes Mediate Secondary Injury, Neurocognitive Outcome, and Neutrophil Infiltration after Traumatic Brain Injury.

Hadijat M Makinde, Carla M Cuda, Talia B Just, Harris R Perlman, Steven J Schwulst

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 2 pooled it
6.7field-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

66 citing papers in PubMed, 2 syntheses or guidelines pooled it, 118 citations in OpenAlex.

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6 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

5 authors at 1 institution in 1 country.

Hadijat M MakindeDivision of Trauma and Critical Care, Department of Surgery, Northwestern University, Chicago, IL 60611; and.
Carla M CudaDivision of Rheumatology, Department of Medicine, Northwestern University, Chicago, IL 60611.
Talia B JustDivision of Trauma and Critical Care, Department of Surgery, Northwestern University, Chicago, IL 60611; and.ORCID 0000-0002-6372-7974
Harris R PerlmanDivision of Rheumatology, Department of Medicine, Northwestern University, Chicago, IL 60611.
Steven J SchwulstDivision of Trauma and Critical Care, Department of Surgery, Northwestern University, Chicago, IL 60611; and s-schwulst@northwestern.edu.ORCID 0000-0003-4248-8545
Northwestern University · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
Tissue resident macrophages regulate proteostasis in the aging lungP01AG049665 · NIA · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Benjamin David Singer · 2015 to 2026
$26.9M
POSTDOCTORAL RHEUMATOLOGY TRAININGT32AR007611 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PERLMAN, HARRIS R · 2001 to 2022
$4.4M
Macrophage Modulation of Lung FibrosisR01HL134375 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PERLMAN, HARRIS R · 2017 to 2020
$2.9M
Development of a Novel RA/Atherosclerosis Mouse ModelR01AR064546 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PERLMAN, HARRIS R · 2013 to 2017
$1.6M
The role of innate immunity in the traumatic brain injury-induced immune suppression syndromeK08GM117341 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SCHWULST, STEVEN J · 2015 to 2018
$763k
Caspase 8: A Novel Suppressor of Dendritic Cell-Mediated AutoimmunityK01AR064313 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CUDA, CARLA M · 2013 to 2017
$597k
RhEumatoid Arthritis SynOvial tissue Network (REASON)UH2AR067687 · NIAMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PERLMAN, HARRIS R, POPE, RICHARD M. · 2014 to 2015
$544k
NCATS NIH HHS UL1 TR001422NHLBI NIH HHS R01 HL134375NIAMS NIH HHS K01 AR064313NIAMS NIH HHS R01 AR064546NIAMS NIH HHS T32 AR007611NIAMS NIH HHS UH2 AR067687NIA NIH HHS P01 AG049665NIGMS NIH HHS K08 GM117341
6 · The paper itself

Abstract

Traumatic brain injury (TBI) results in rapid recruitment of leukocytes into the injured brain. Monocytes constitute a significant proportion of the initial infiltrate and have the potential to propagate secondary brain injury or generate an environment of repair and regeneration. Monocytes are a diverse population of cells (classical, intermediate, and nonclassical) with distinct functions, however, the recruitment order of these subpopulations to the injured brain largely remains unknown. Thus, we examined which monocyte subpopulations are required for the generation of early inflammatory infiltrate within the injured brain, and whether their depletion attenuates secondary injury or neurocognitive outcome. Global monocyte depletion correlated with significant improvements in brain edema, motor coordination, and working memory, and abrogated neutrophil infiltration into the injured brain. However, targeted depletion of classical monocytes alone had no effect on neutrophil recruitment to the site of injury, implicating the nonclassical monocyte in this process. In contrast, mice that have markedly reduced numbers of nonclassical monocytes (CX3CR1

Indexed as

Neutrophil InfiltrationAnimalsBrain Injuries, TraumaticCellular MicroenvironmentCX3C Chemokine Receptor 1EdemaHumansMacrophagesMemory, Short-TermMiceMice, Inbred C57BLMice, KnockoutNeurocognitive DisordersNeutrophilsPsychomotor PerformanceCX3C Chemokine Receptor 1Cx3cr1 protein, mouse

Identifiers

PMID28993515
PMCPMC5679470
OpenAlexW2764063727

What OpenQuestion holds

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LicenceTDM
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.