Evidence map›Paper›PMID 31138214›Full record

ArticleJournal of neuroinflammation2019

Contribution of LTi and T

Verena Schropp, Jörn Rohde, Damiano M Rovituso, Samir Jabari, Richa Bharti, Stefanie Kuerten

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  5. DEPs Induce Local Ige Class Switching Independent of Their Ability to Stimulate iBALT de Novo Formation.International journal of environmental research and public health · 2022
    Article
  6. Review
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  8. Article
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  11. Bcl6 controls meningeal Th17-B cell interaction in murine neuroinflammation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Review
  13. 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 3 institutions in 1 country.

Verena SchroppInstitute of Anatomy, Chair of Anatomy and Cell Biology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Jörn RohdeInstitute of Anatomy and Cell Biology, University of Würzburg, Würzburg, Germany.
Damiano M RovitusoInstitute of Anatomy and Cell Biology, University of Würzburg, Würzburg, Germany.
Samir JabariInstitute of Anatomy, Chair of Anatomy and Cell Biology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany.
Richa BhartiCore Unit Systems Medicine, University Hospitals of Würzburg, Würzburg, Germany.
Stefanie KuertenInstitute of Anatomy, Chair of Anatomy and Cell Biology, Friedrich-Alexander University Erlangen-Nürnberg (FAU), Erlangen, Germany. stefanie.kuerten@fau.de.ORCID http://orcid.org/0000-0001-6119-605X
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversity of Würzburg · DEUniversitätsklinikum Würzburg · DE

Funding

Deutsche Forschungsgemeinschaft KU2760/4-1
6 · The paper itself

Abstract

backgroundIn a subgroup of patients suffering from progressive multiple sclerosis (MS), which is an inflammation-mediated neurodegenerative disease of the central nervous system (CNS), B cell aggregates were discovered within the meninges. Occurrence of these structures was associated with a more severe disease course and cortical histopathology. We have developed the B cell-dependent MP4-induced experimental autoimmune encephalomyelitis (EAE) as a mouse model to mimic this trait of the human disease. The aim of this study was to determine a potential role of lymphoid tissue inducer (LTi) and T

methodsWe performed flow cytometry of cerebellar and splenic tissue of MP4-immunized mice in the acute and chronic stage of the disease to analyze the presence of CD3

resultsWhile we were able to detect LTi cells in the embryonic spleen and adult intestine, which served as positive controls, there was no evidence for the existence of such a population in acute or chronic EAE in neither of the two models. Yet, we detected CD3

conclusionThe absence of LTi cells in the cerebellum suggests that other cells might take over the function as an initiator of lymphoid tissue formation in the CNS. Overall, the development of ectopic lymphoid organs is a complex process based on an interplay between several molecules and signals. Here, we propose some potential candidates, which might be involved in the formation of B cell aggregates in the CNS of MP4-immunized mice.

Indexed as

Disease Models, AnimalAnimalsB-LymphocytesCell AggregationCentral Nervous SystemEncephalomyelitis, Autoimmune, ExperimentalFemaleImmunity, InnateLymphoid TissueMiceMice, Inbred C57BLMultiple SclerosisPregnancyTh17 CellsEAELTi cellsMP4MSTH17 cells

Identifiers

PMID31138214
PMCPMC6540524
OpenAlexW2947434135

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.