Evidence map›Paper›PMID 36446955›Full record

ReviewSeminars in immunopathology2023

The immunopathology of B lymphocytes during stroke-induced injury and repair.

Mary K Malone, Thomas A Ujas, Daimen R S Britsch, Katherine M Cotter, Katie Poinsatte, Ann M Stowe

Open access · hybridAbstract readReview
In one paragraph

Review in Seminars in immunopathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 36 citations in OpenAlex.

  1. Systemic inflammatory profiles associated with early EEG abnormalities following ischemic stroke: a cohort study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
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  18. CD19Frontiers in immunology · 2025
    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

6 authors at 2 institutions in 1 country.

Mary K MaloneDepartment of Neuroscience, The University of Kentucky, Lexington, KY, USA.ORCID 0000-0003-0183-6427
Thomas A UjasDepartment of Neuroscience, The University of Kentucky, Lexington, KY, USA.ORCID 0000-0001-8512-8369
Daimen R S BritschDepartment of Neuroscience, The University of Kentucky, Lexington, KY, USA.
Katherine M CotterDepartment of Neuroscience, The University of Kentucky, Lexington, KY, USA.
Katie PoinsatteDepartment of Neurology & Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Ann M StoweDepartment of Neuroscience, The University of Kentucky, Lexington, KY, USA. ann.stowe@uky.edu.ORCID 0000-0001-8111-4429
University of Kentucky · USThe University of Texas Southwestern Medical Center · US

Funding

University of Kentucky Alzheimer's Disease Research CenterP30AG072946 · NIA · UNIVERSITY OF KENTUCKY · PI LINDA J VAN ELDIK · 2021 to 2026
$23.5M
B Cells Directly Alter Adaptive Plasticity to Support Functional Recovery After StrokeR01NS088555 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI STOWE, ANN MARIE · 2015 to 2025
$2.8M
Neurobiology of CNS Injury and RepairT32NS077889 · NINDS · UNIVERSITY OF KENTUCKY · PI Warren Joseph Alilain, JOHN C GENSEL · 2012 to 2026
$2.4M
Training in Translational Research in Alzheimer's and Related Dementias (TRIAD)T32AG078110 · NIA · UNIVERSITY OF KENTUCKY · PI Michael Paul Murphy, LINDA J VAN ELDIK · 2022 to 2026
$2.3M
Training in Translational Research in Alzheimer's and Related Dementias (TRIAD)T32AG057461 · NIA · UNIVERSITY OF KENTUCKY · PI MURPHY, MICHAEL PAUL, VAN ELDIK, LINDA J · 2017 to 2021
$2.1M
Diversity Supplement: B Cells Directly Alter Adaptive Plasticity to Support Functional Recovery After StrokeRF1NS088555 · NINDS · UNIVERSITY OF KENTUCKY · PI STOWE, ANN MARIE · 2021 to 2023
$1.3M
NIA NIH HHS P30 AG072946NIA NIH HHS T32 AG057461NIA NIH HHS T32 AG078110NINDS NIH HHS R01 NS088555NINDS NIH HHS RF1 NS088555NINDS NIH HHS T32 NS077889
6 · The paper itself

Abstract

B cells, also known as B lymphocytes or lymphoid lineage cells, are a historically understudied cell population with regard to brain-related injuries and diseases. However, an increasing number of publications have begun to elucidate the different phenotypes and roles B cells can undertake during central nervous system (CNS) pathology, including following ischemic and hemorrhagic stroke. B cell phenotype is intrinsically linked to function following stroke, as they may be beneficial or detrimental depending on the subset, timing, and microenvironment. Factors such as age, sex, and presence of co-morbidity also influence the behavior of post-stroke B cells. The following review will briefly describe B cells from origination to senescence, explore B cell function by integrating decades of stroke research, differentiate between the known B cell subtypes and their respective activity, discuss some of the physiological influences on B cells as well as the influence of B cells on certain physiological functions, and highlight the differences between B cells in healthy and disease states with particular emphasis in the context of ischemic stroke.

Indexed as

StrokeB-LymphocytesHumansAdaptive immunityAge-associated B cellsAntibodiesIschemic strokeMeningesNeuroimmune

Identifiers

PMID36446955
PMCPMC9708141
OpenAlexW4310458578

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.