Evidence map›Paper›PMID 36587195›Full record

ArticleJournal of neuroinflammation2022

Expansion of regulatory T cells by CD28 superagonistic antibodies attenuates neurodegeneration in A53T-α-synuclein Parkinson's disease mice.

Mohammad Badr, Rhonda L McFleder, Jingjing Wu, Susanne Knorr, James B Koprich, Thomas Hünig, Jonathan M Brotchie, Jens Volkmann, Manfred B Lutz, Chi Wang Ip

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

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  16. Brain regulatory T cells.Nature reviews. Immunology · 2024
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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

10 authors at 4 institutions in 2 countries.

Mohammad Badr *Department of Neurology, University Hospital of Würzburg, Würzburg, Germany.
Rhonda L McFleder *Department of Neurology, University Hospital of Würzburg, Würzburg, Germany.
Jingjing WuDepartment of Neurology, University Hospital of Würzburg, Würzburg, Germany.
Susanne KnorrDepartment of Neurology, University Hospital of Würzburg, Würzburg, Germany.
James B KoprichKrembil Research Institute, Toronto Western Hospital, University Health Network, Toronto, ON, Canada.
Thomas HünigInstitute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
Jonathan M BrotchieKrembil Research Institute, Toronto Western Hospital, University Health Network, Toronto, ON, Canada.
Jens VolkmannDepartment of Neurology, University Hospital of Würzburg, Würzburg, Germany.
Manfred B LutzInstitute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
Chi Wang IpDepartment of Neurology, University Hospital of Würzburg, Würzburg, Germany. ip_c@ukw.de.
Universitätsklinikum Würzburg · DEUniversity of Würzburg · DEKrembil Research InstituteToronto Western Hospital · CA

Funding

Deutsche Forschungsgemeinschaft 424778381-TRR 295 (A06) (A01)Interdisziplinäres Zentrum für Klinische Forschung, Universitätsklinikum Würzburg A-303; A-421; N-362
6 · The paper itself

Abstract

backgroundRegulatory CD4

methodsUsing the AAV1/2-A53T-α-synuclein Parkinson's disease mouse model that overexpresses the pathogenic human A53T-α-synuclein (hαSyn) variant in dopaminergic neurons of the substantia nigra, we assessed the neuroprotective and disease-modifying efficacy of a single intraperitoneal dose of CD28SA given at an early disease stage.

resultsCD28SA led to Treg expansion 3 days after delivery in hαSyn Parkinson's disease mice. At this timepoint, an early pro-inflammation was observed in vehicle-treated hαSyn Parkinson's disease mice with elevated percentages of CD8

conclusionsOur data indicate that immune modulation by Treg expansion at a timepoint of overt inflammation is effective for treatment of hαSyn Parkinson's disease mice and suggest that the concept of early immune therapy could pose a disease-modifying option for Parkinson's disease patients.

Indexed as

Parkinson Diseasealpha-SynucleinAnimalsAntibodiesCD28 AntigensCD8-Positive T-LymphocytesDisease Models, AnimalDopamineDopaminergic NeuronsHumansMiceMice, Inbred C57BLSubstantia NigraT-Lymphocytes, Regulatoryalpha-SynucleinAntibodiesCD28 AntigensDopamineNeuroinflammationNeuroprotectionParkinson’s diseaseRegulatory T cellsT cells

Identifiers

PMID36587195
PMCPMC9805693
OpenAlexW4313335453

What Socratic 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 Socratic graph.