Evidence map›Paper›PMID 31842667›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2020

Early neutrophil infiltration is critical for inflammation-sensitized hypoxic-ischemic brain injury in newborns.

Hui-Wen Yao, Chia-Yi Kuan

Abstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
–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

31 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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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

2 authors.

Hui-Wen YaoDepartment of Neuroscience and the Center for Brain Immunology and Glia (BIG), University of Virginia School of Medicine, Charlottesville, VA, USA.
Chia-Yi KuanDepartment of Neuroscience and the Center for Brain Immunology and Glia (BIG), University of Virginia School of Medicine, Charlottesville, VA, USA.

Funding

Treating neurotoxicity and cognitive deficits due to hyperphosphorylated tau.R01NS135693 · NINDS · UNIVERSITY OF VIRGINIA · PI Chia-Yi Kuan, Min-Hao Kuo · 2023 to 2026
$2.4M
Creatine Transporter Deficiency and Brain EnergeticsR01NS108763 · NINDS · UNIVERSITY OF VIRGINIA · PI KUAN, CHIA-YI · 2018 to 2022
$2.3M
Crosstalk of Innate and Adaptive Immunity in Infection-Sensitized Neonatal HIER01NS095064 · NINDS · UNIVERSITY OF VIRGINIA · PI KUAN, CHIA-YI · 2016 to 2020
$1.7M
Mechanisms and Experimental Therapy of Perinatal Cerebral HemorrhageR01NS084744 · NINDS · UNIVERSITY OF VIRGINIA · PI KUAN, CHIA-YI · 2014 to 2018
$1.7M
Monocyte-Derived Microglia after Maternal Immune Activation and Neonatal BrainInjuryR21NS100419 · NINDS · UNIVERSITY OF VIRGINIA · PI KUAN, CHIA-YI · 2017 to 2018
$429k
NINDS NIH HHS R01 NS084744NINDS NIH HHS R01 NS095064NINDS NIH HHS R01 NS108763NINDS NIH HHS R01 NS135693NINDS NIH HHS R21 NS100419
6 · The paper itself

Abstract

Neutrophils are the most abundant leukocytes and usually the first immune cell-type recruited to a site of infection or tissue damage. In asphyxiated neonates, elevated peripheral neutrophil counts are associated with poorer neurological outcomes. Induced neutropenia provides brain protection in animal models of neonatal hypoxic-ischemic (HI) injury, but the anti-neutrophil serum used in past studies heavily cross-reacts with monocytes, thus complicating the interpretation of results. Here we examined neutrophil influx and extravasation, and used a specific anti-Ly6G antibody for induced neutropenia against lipopolysaccharide (LPS)-pretreated HI injury in murine neonates, a model for inflammation-sensitized hypoxic-ischemic encephalopathy (HIE). As early as 6 h after the LPS/HI insult, the mRNAs for neutrophil-recruiting and mitogenic chemokines ascended in the ipsilateral hemisphere, coinciding with immuno-detection of neutrophils. However, neutrophils mainly resided within blood vessels, exhibiting signs for neutrophil extracellular traps (NETs), before 48 h post-LPS/HI. Prophylactic anti-Ly6G treatment blocked the brain infiltration of neutrophils, but not monocytes or lymphocytes, and markedly decreased LPS/HI-induced pro-inflammatory cytokines, matrix metalloproteinase 9 (MMP-9), and brain tissue loss. In contrast, anti-Ly6G treatment at 4 h post-LPS/HI failed to prevent the influx of neutrophils and brain damage. Together, these results suggest important pathological functions for early-arriving neutrophils in inflammation-sensitized HIE.

Indexed as

Neutrophil InfiltrationAnimalsAnimals, NewbornAntigens, LyBiomarkersBrain InjuriesChemotaxis, LeukocyteCytokinesDisease Models, AnimalDisease SusceptibilityExtracellular TrapsFluorescent Antibody TechniqueHypoxia-Ischemia, BrainImmunohistochemistryInflammationLipopolysaccharidesAntigens, LyBiomarkersCytokinesLipopolysaccharidesLy6G antigen, mouseMatrix Metalloproteinasesanti-Ly6GHypoxic-ischemic encephalopathylipopolysaccharidematrix metalloproteinasesneutrophil extracellular trap

Identifiers

PMID31842667
PMCPMC7585929

What OpenQuestion holds

Textmetadata
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.