Evidence map›Paper›PMID 32237074›Full record

ReviewCNS neuroscience & therapeutics2020

Spleen participation in partial MHC class II construct neuroprotection in stroke.

John Brown, Chase Kingsbury, Jea-Young Lee, Arthur A Vandenbark, Roberto Meza-Romero, Halina Offner, Cesar V Borlongan

Open access · goldAbstract readReview
In one paragraph

Review in CNS neuroscience & therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Updates of the role of B-cells in ischemic stroke.Frontiers in cellular neuroscience · 2024
    Review
  4. Review
  5. Reversal of the detrimental effects of social isolation on ischemic cerebral injury and stroke-associated pneumonia by inhibiting small intestinalJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Article
  6. CNS-peripheral immune interactions in hemorrhagic stroke.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Review
  7. RAGE-mediated T cell metabolic reprogramming shapes T cell inflammatory response after stroke.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. 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

7 authors at 2 institutions in 1 country.

John BrownDepartment of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, University of South Florida College of Medicine, Tampa, FL, USA.
Chase KingsburyDepartment of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, University of South Florida College of Medicine, Tampa, FL, USA.
Jea-Young LeeDepartment of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, University of South Florida College of Medicine, Tampa, FL, USA.
Arthur A VandenbarkNeuroimmunology Research R&D-31, VA Portland Health Care System, Portland, OR, USA.
Roberto Meza-RomeroNeuroimmunology Research R&D-31, VA Portland Health Care System, Portland, OR, USA.
Halina OffnerNeuroimmunology Research R&D-31, VA Portland Health Care System, Portland, OR, USA.
Cesar V BorlonganDepartment of Neurosurgery and Brain Repair, Center of Excellence for Aging and Brain Repair, University of South Florida College of Medicine, Tampa, FL, USA.ORCID 0000-0002-2966-9782
University of South Florida · USOregon Health & Science University · US

Funding

Development of DRα1-MOG-35-55 for treatment of DR2 negative MS subjectsR42AI122574 · NIAID · VIROGENOMICS BIODEVELOPMENT, INC. · PI VANDENBARK, ARTHUR A. · 2017 to 2018
$1.5M
BLRD VA I01 BX000226BLRD VA I01 BX005112BLRD VA IK6 BX004209NIAID NIH HHS R42 AI122574
6 · The paper itself

Abstract

Pathological progression of stroke in the peripheral and central nervous systems (PNS and CNS) is characterized by multiple converging signalling pathways that exacerbate neuroinflammation-mediated secondary cell death. This creates a need for a novel type of immunotherapy capable of simultaneously lowering the synergistic inflammatory responses in the PNS and CNS, specifically the spleen and brain. Previously, we demonstrated that partial major histocompatibility complex (MHC) class II constructs can be administered subcutaneously to promote histological and behavioural effects that alleviate common symptoms found in a murine model of transient stroke. This MHC class II manipulates T cell cytokine expression in both PNS and CNS, resulting in dampened inflammation. In our long-standing efforts towards translational research, we recently demonstrated that a potent next generation mouse-based partial MHC class II construct named DRmQ (DRa1

Indexed as

AnimalsHistocompatibility Antigens Class IIHumansImmunityNeuroprotectionSpleenStrokeHistocompatibility Antigens Class IIcerebral ischaemiacytokinesimmune responsemajor histocompatibility complex class IImiddle cerebral artery occlusionregenerative medicinespleen

Identifiers

PMID32237074
PMCPMC7298973
OpenAlexW3014345075

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.