Evidence map›Paper›PMID 33042113›Full record

ReviewFrontiers in immunology2020

Communications Between Peripheral and the Brain-Resident Immune System in Neuronal Regeneration After Stroke.

Fangxi Liu, Xi Cheng, Shanshan Zhong, Chang Liu, Jukka Jolkkonen, Xiuchun Zhang, Yifan Liang, Zhouyang Liu, Chuansheng Zhao

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
2.1field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 3 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  4. Article
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  9. Modified human mesenchymal stromal/stem cells restore cortical excitability after focal ischemic stroke in rats.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  10. Review
  11. Review
  12. Inflammaging and Brain Aging.International journal of molecular sciences · 2024
    Review
  13. Article
  14. Splenectomy does not affect mouse behaviors.Neural regeneration research · 2023
    Article
  15. Article
  16. Review
  17. Article
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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

9 authors at 3 institutions in 2 countries.

Fangxi LiuNeurology, The First Hospital of China Medical University, Shenyang, China.
Xi ChengNeurology, The First Hospital of China Medical University, Shenyang, China.
Shanshan ZhongNeurology, The First Hospital of China Medical University, Shenyang, China.
Chang LiuNeurology, The First Hospital of China Medical University, Shenyang, China.
Jukka JolkkonenA.I. Virtanen Institute and Institute of Clinical Medicine/Neurology, University of Eastern Finland, Kuopio, Finland.
Xiuchun ZhangNeurology, The First Hospital of China Medical University, Shenyang, China.
Yifan LiangNeurology, The First Hospital of China Medical University, Shenyang, China.
Zhouyang LiuNeurology, The First Hospital of China Medical University, Shenyang, China.
Chuansheng ZhaoNeurology, The First Hospital of China Medical University, Shenyang, China.
China Medical University · CNFirst Hospital of China Medical University · CNUniversity of Eastern Finland · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral ischemia may cause irreversible neural network damage and result in functional deficits. Targeting neuronal repair after stroke potentiates the formation of new connections, which can be translated into a better functional outcome. Innate and adaptive immune responses in the brain and the periphery triggered by ischemic damage participate in regulating neural repair after a stroke. Immune cells in the blood circulation and gut lymphatic tissues that have been shaped by immune components including gut microbiota and metabolites can infiltrate the ischemic brain and, once there, influence neuronal regeneration either directly or by modulating the properties of brain-resident immune cells. Immune-related signalings and metabolites from the gut microbiota can also directly alter the phenotypes of resident immune cells to promote neuronal regeneration. In this review, we discuss several potential mechanisms through which peripheral and brain-resident immune components can cooperate to promote first the resolution of neuroinflammation and subsequently to improved neural regeneration and a better functional recovery. We propose that new insights into discovery of regulators targeting pro-regenerative process in this complex neuro-immune network may lead to novel strategies for neuronal regeneration.

Indexed as

Nerve RegenerationNeuroimmunomodulationAnimalsBrainGastrointestinal MicrobiomeHumansImmune SystemNeuronsRecovery of FunctionSignal TransductionStrokebraincommunicationgut microbiotaimmune systemneuronal regenerationperipheralstroke

Identifiers

PMID33042113
PMCPMC7530165
OpenAlexW3087015595

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.