Evidence map›Paper›PMID 31715458›Full record

ArticleJournal of neuroimmunology2020

B cell function impacts the efficacy of IFN-β therapy in EAE.

Agnieshka M Agasing, Saurabh Gawde, Gaurav Kumar, Emma Turner, Robert C Axtell

Open access · hybridAbstract read
In one paragraph

Article in Journal of neuroimmunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-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

9 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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  9. Human CommensalFrontiers in immunology · 2020
    Article
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

5 authors at 3 institutions in 1 country.

Agnieshka M AgasingDepartment of Arthritis and Clinical Immunology Research, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA; Department of Microbiology and Immunology, Oklahoma University Health Science Center, Oklahoma City, OK, USA.
Saurabh GawdeDepartment of Arthritis and Clinical Immunology Research, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA; Department of Microbiology and Immunology, Oklahoma University Health Science Center, Oklahoma City, OK, USA.
Gaurav KumarDepartment of Microbiology and Immunology, Oklahoma University Health Science Center, Oklahoma City, OK, USA.
Emma TurnerDepartment of Microbiology and Immunology, Oklahoma University Health Science Center, Oklahoma City, OK, USA.
Robert C AxtellDepartment of Microbiology and Immunology, Oklahoma University Health Science Center, Oklahoma City, OK, USA. Electronic address: bob-axtell@omrf.org.
University of Oklahoma Health Sciences Center · USOklahoma Medical Research Foundation · USOU Health

Funding

Understanding the roles type I Interferon and TH17 play in Neuromyelitis Optica and other autoimmune diseases.R01AI137047 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI AXTELL, ROBERT C · 2018 to 2021
$2.8M
Pathogenic B cell and T helper cell interactions in Neuromyelitis OpticaR01EY027346 · NEI · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI AXTELL, ROBERT C · 2017 to 2021
$2.2M
NEI NIH HHS R01 EY027346NIAID NIH HHS R01 AI137047
6 · The paper itself

Abstract

Recent studies identified that interferon beta (IFN-β) treatment skews B-cells towards a regulatory phenotype in multiple sclerosis. To assess B cell involvement during IFN-β therapy, we compared IFN-β treatment in a B cell-independent model and a B cell-dependent model of experimental autoimmune encephalomyelitis (EAE). We show that in B cell-independent EAE, IFN-β ameliorates neuroinflammation. Conversely, in B cell-dependent EAE, IFN-β has no effect on disease. Effective IFN-β therapy in B cell-independent EAE was associated with reduced inflammatory T cells in the CNS and skewed splenic B cells towards an immature population and away from a germinal center population. These immune cell populations were unchanged in B cell-dependent EAE. Finally, we found that IFN-β increased marginal zone B cells in both EAE models. These findings indicate that B cell function impacts IFN-β efficacy during neuroinflammation.

Indexed as

AnimalsB-LymphocytesEncephalomyelitis, Autoimmune, ExperimentalFemaleInterferon-betaMiceMice, Inbred C57BLMyelin-Oligodendrocyte GlycoproteinInterferon-betaMyelin-Oligodendrocyte Glycoprotein

Identifiers

PMID31715458
PMCPMC6911824
OpenAlexW2983543527

What OpenQuestion holds

Textmetadata
LicenceTDM
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.