Evidence map›Paper›PMID 26581581›Full record

ArticleJournal of neuroinflammation2015

Endogenous IFN-β signaling exerts anti-inflammatory actions in experimentally induced focal cerebral ischemia.

Ana R Inácio, Yawei Liu, Bettina H Clausen, Martina Svensson, Krzysztof Kucharz, Yiyi Yang, Totte Stankovich, Reza Khorooshi, Kate L Lambertsen, Shohreh Issazadeh-Navikas and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Inflammatory Responses After Ischemic Stroke.Seminars in immunopathology · 2022
    Review
  11. Article
  12. Gene Expression Profile ofFrontiers in medicine · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Current advances in ischemic stroke research and therapies.Biochimica et biophysica acta. Molecular basis of disease · 2020
    Review
  18. Review
  19. Article
  20. Therapeutic spectrum of interferon-β in ischemic stroke.Journal of neuroscience research · 2019
    Review
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

11 authors at 4 institutions in 3 countries.

Ana R InácioLaboratory for Experimental Brain Research, Department of Clinical Sciences, Lund University, BMC A13, Sölvegatan 17, 22184, Lund, Sweden. ana.inacio@inserm.fr.
Yawei LiuNeuroinflammation Unit, Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.
Bettina H ClausenDepartment of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, JB Winsloewsvej 21, st + 25, 2, 5000, Odense C, Denmark.
Martina SvenssonExperimental Neuroinflammation Laboratory, Department of Experimental Medical Sciences, Lund University, BMC B11, Sölvegatan 19, 22184, Lund, Sweden.
Krzysztof KucharzLaboratory for Experimental Brain Research, Department of Clinical Sciences, Lund University, BMC A13, Sölvegatan 17, 22184, Lund, Sweden.
Yiyi YangExperimental Neuroinflammation Laboratory, Department of Experimental Medical Sciences, Lund University, BMC B11, Sölvegatan 19, 22184, Lund, Sweden.
Totte StankovichLaboratory for Experimental Brain Research, Department of Clinical Sciences, Lund University, BMC A13, Sölvegatan 17, 22184, Lund, Sweden.
Reza KhorooshiDepartment of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, JB Winsloewsvej 21, st + 25, 2, 5000, Odense C, Denmark.
Kate L LambertsenDepartment of Neurobiology Research, Institute of Molecular Medicine, University of Southern Denmark, JB Winsloewsvej 21, st + 25, 2, 5000, Odense C, Denmark.
Shohreh Issazadeh-NavikasNeuroinflammation Unit, Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark. shohreh.issazadeh@bric.ku.dk.
Tomas DeierborgLaboratory for Experimental Brain Research, Department of Clinical Sciences, Lund University, BMC A13, Sölvegatan 17, 22184, Lund, Sweden.
Lund University · SEUniversity of Southern Denmark · DKUniversity of Copenhagen · DKCentre d’Immunologie de Marseille-Luminy · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInterferon (IFN)-β exerts anti-inflammatory effects, coupled to remarkable neurological improvements in multiple sclerosis, a neuroinflammatory condition of the central nervous system. Analogously, it has been hypothesized that IFN-β, by limiting inflammation, decreases neuronal death and promotes functional recovery after stroke. However, the core actions of endogenous IFN-β signaling in stroke are unclear.

methodsTo address this question, we used two clinically relevant models of focal cerebral ischemia, transient and permanent middle cerebral artery occlusion, and two genetically modified mouse lines, lacking either IFN-β or its receptor, the IFN-α/β receptor. Subsets of inflammatory and immune cells isolated from the brain, blood, and spleen were studied using flow cytometry. Sensorimotor deficits were assessed by a modified composite neuroscore, the rotating pole and grip strength tests, and cerebral infarct volumes were given by lack of neuronal nuclei immunoreactivity.

resultsHere, we report alterations in local and systemic inflammation in IFN-β knockout (IFN-βKO) mice over 8 days after induction of focal cerebral ischemia. Notably, IFN-βKO mice showed a higher number of infiltrating leukocytes in the brain 2 days after stroke. Concomitantly, in the blood of IFN-βKO mice, we found a higher percentage of total B cells but a similar percentage of mature and activated B cells, collectively indicating a higher proliferation rate. The additional differential regulation of circulating cytokines and splenic immune cell populations in wild-type and IFN-βKO mice further supports an important immunoregulatory function of IFN-β in stroke. Moreover, we observed a significant weight loss 2-3 days and a reduction in grip strength 2 days after stroke in the IFN-βKO group, while endogenous IFN-β signaling did not affect the infarct volume.

conclusionsWe conclude that endogenous IFN-β signaling attenuates local inflammation, regulates peripheral immune cells, and, thereby, may contribute positively to stroke outcome.

Indexed as

Interferon-betaAnimalsB-LymphocytesBrainBrain IschemiaCytokinesHand StrengthInfarction, Middle Cerebral ArteryInflammationIschemic Attack, TransientLeukocytesLymphocyte CountMaleMiceMice, Inbred C57BLMice, KnockoutCytokinesInterferon-betaReceptors, Interferon

Identifiers

PMID26581581
PMCPMC4652356
OpenAlexW2176625493

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LicenceCC BY
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Registered trials

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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.