Evidence map›Paper›PMID 31130183›Full record

ReviewCellular immunology2019

The role of B cells in multiple sclerosis: Current and future therapies.

Austin Negron, Rachel R Robinson, Olaf Stüve, Thomas G Forsthuber

Abstract readReview
In one paragraph

Review in Cellular immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Article
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  20. Intrathecally produced CXCL13: A predictive biomarker in multiple sclerosis.Multiple sclerosis journal - experimental, translational and clinical
    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

4 authors.

Austin NegronDepartment of Biology, University of Texas at San Antonio, TX 78249, USA.
Rachel R RobinsonDepartment of Biology, University of Texas at San Antonio, TX 78249, USA.
Olaf StüveDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, TX, USA; Neurology Section, VA North Texas Health Care System, Medical Service, Dallas, TX, USA.
Thomas G ForsthuberDepartment of Biology, University of Texas at San Antonio, TX 78249, USA. Electronic address: thomas.forsthuber@utsa.edu.

Funding

UTSA RISE Research Training ProgramR25GM060655 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI BAREA-RODRIGUEZ, EDWIN J · 2000 to 2022
$21.6M
RCMI Center for Interdiscplinary Health Research CIHRG12MD007591 · NIMHD · UNIVERSITY OF TEXAS SAN ANTONIO · PI PERRY, GEORGE · 2012 to 2016
$10.4M
Avidity Maturation of T Cells in Mutiple SclerosisR01NS042809 · NINDS · UNIVERSITY OF TEXAS SAN ANTONIO · PI FORSTHUBER, THOMAS G. · 2002 to 2005
$1.0M
Eliminating autoantibody-producing plasma cells in neuroinflammation via ERK inhibitionR21AI144731 · NIAID · UNIVERSITY OF TEXAS SAN ANTONIO · PI FORSTHUBER, THOMAS G. · 2019 to 2020
$411k
Predictive biomarkers for EAE developmentR21NS084201 · NINDS · UNIVERSITY OF TEXAS SAN ANTONIO · PI FORSTHUBER, THOMAS G. · 2014 to 2015
$404k
NIAID NIH HHS R21 AI144731NIGMS NIH HHS R25 GM060655NIMHD NIH HHS G12 MD007591NINDS NIH HHS R01 NS042809NINDS NIH HHS R21 NS084201
6 · The paper itself

Abstract

While it was long held that T cells were the primary mediators of multiple sclerosis (MS) pathogenesis, the beneficial effects observed in response to treatment with Rituximab (RTX), a monoclonal antibody (mAb) targeting CD20, shed light on a key contributor to MS that had been previously underappreciated: B cells. This has been reaffirmed by results from clinical trials testing the efficacy of subsequently developed B cell-depleting mAbs targeting CD20 as well as studies revisiting the effects of previous disease-modifying therapies (DMTs) on B cell subsets thought to modulate disease severity. In this review, we summarize current knowledge regarding the complex roles of B cells in MS pathogenesis and current and potential future B cell-directed therapies.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CD20B-Lymphocyte SubsetsHumansMultiple SclerosisRituximabAntibodies, MonoclonalAntigens, CD20Rituximab

Identifiers

PMID31130183
PMCPMC6540809

What OpenQuestion holds

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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.