Evidence map›Paper›PMID 27485238›Full record

ReviewNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2016

Microglia and Monocyte-Derived Macrophages in Stroke.

Eunhee Kim, Sunghee Cho

Open access · bronzeAbstract readReview
In one paragraph

Review in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

91 citing papers in PubMed, 153 citations in OpenAlex.

  1. The role of type I collagen in white matter injury.Anatomical science international · 2026
    Review
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  6. Injury to repair: Functions of microglia and monocyte-derived cells in ischemic stroke.Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association · 2025
    Review
  7. Article
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  13. Detrimental influence of Arginase-1 in infiltrating macrophages on poststroke functional recovery and inflammatory milieu.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Review
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31 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

2 authors at 2 institutions in 1 country.

Eunhee KimFeil Family Brain and Mind Research Institute, Weill Cornell Medicine at Burke Medical Research Institute, White Plains, NY, 10605, USA.
Sunghee ChoFeil Family Brain and Mind Research Institute, Weill Cornell Medicine at Burke Medical Research Institute, White Plains, NY, 10605, USA. suc2002@med.cornell.edu.
Burke Medical Research Institute · USCornell University · US

Funding

The role of CD36 in ischemic inflammation and injuryR01HL082511 · NHLBI · WINIFRED MASTERSON BURKE MED RES INST · PI CHO, SUNGHEE · 2006 to 2014
$4.4M
Role of CD36 in functional recovery in chronic strokeR01NS095359 · NINDS · WINIFRED MASTERSON BURKE MED RES INST · PI CHO, SUNGHEE · 2015 to 2019
$2.1M
Impact of BDNF SNP on stroke-induced plasticity and motor functionR01NS077897 · NINDS · WINIFRED MASTERSON BURKE MED RES INST · PI CHO, SUNGHEE · 2012 to 2016
$2.0M
NHLBI NIH HHS R01 HL082511NINDS NIH HHS R01 NS077897NINDS NIH HHS R01 NS095359
6 · The paper itself

Abstract

Historically, the brain has been considered an immune-privileged organ separated from the peripheral immune system by the blood-brain barrier. However, immune responses do occur in the brain in neurological conditions in which the integrity of the blood-brain barrier is compromised, exposing the brain to peripheral antigens and endogenous danger signals. While most of the associated pathological processes occur in the central nervous system, it is now clear that peripheral immune cells, especially mononuclear phagocytes, that infiltrate into the injury site play a key role in modulating the progression of primary brain injury development. As inflammation is a necessary and critical component for the subsequent injury resolution process, understanding the contribution of mononuclear phagocytes on the regulation of inflammatory responses may provide novel approaches for potential therapies. Furthermore, predisposed comorbid conditions at the time of stroke cause the alteration of stroke-induced immune and inflammatory responses and subsequently influence stroke outcome. In this review, we summarize a role for microglia and monocytes/macrophages in acute ischemic stroke in the context of normal and metabolically compromised conditions.

Indexed as

AnimalsBlood-Brain BarrierHumansInflammationMacrophagesMicrogliaStrokeComorbidityInflammationIschemic strokeMicrogliaMonocytes/macrophages

Identifiers

PMID27485238
PMCPMC5081116
OpenAlexW2506572744

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.