Evidence map›Paper›PMID 26511623›Full record

ArticleActa neuropathologica2015

Antibodies produced by clonally expanded plasma cells in multiple sclerosis cerebrospinal fluid cause demyelination of spinal cord explants.

Kevin Blauth, John Soltys, Adeline Matschulat, Cory R Reiter, Alanna Ritchie, Nicholas L Baird, Jeffrey L Bennett, Gregory P Owens

Open access · greenAbstract read
In one paragraph

Article in Acta neuropathologica, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

58 citing papers in PubMed, 93 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Kevin BlauthDepartment of Neurology, University of Colorado Denver, Aurora, CO, USA.
John SoltysDepartment of Neurology, University of Colorado Denver, Aurora, CO, USA.
Adeline MatschulatDepartment of Neurology, University of Colorado Denver, Aurora, CO, USA.
Cory R ReiterDepartment of Neurology, University of Colorado Denver, Aurora, CO, USA.
Alanna RitchieDepartment of Neurology, University of Colorado Denver, Aurora, CO, USA.
Nicholas L BairdDepartment of Neurology, University of Colorado Denver, Aurora, CO, USA.
Jeffrey L BennettDepartment of Neurology, University of Colorado Denver, Aurora, CO, USA.
Gregory P OwensDepartment of Neurology, University of Colorado Denver, Aurora, CO, USA. greg.owens@ucdenver.edu.
University of Colorado Denver · US

Funding

Colorado Clinical and Translational Sciences InstituteUL1TR001082 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2013 to 2017
$48.0M
Medical Scientist Training ProgramT32GM008497 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI WILSON, CARA C. · 1993 to 2022
$15.2M
ZEBRAFISH TRANSGENIC CORE - ROCKY MOUNTAIN NEUROLOGICAL DISORDERS CORE CENTERP30NS048154 · NINDS · UNIVERSITY OF COLORADO DENVER · PI RIBERA, ANGELES BADELL · 2004 to 2020
$10.1M
Humoral Immunity, Astrocyte Injury, and Demyelination in Neuromyelitis OpticaR01EY022936 · NEI · UNIVERSITY OF COLORADO DENVER · PI BENNETT, JEFFREY L · 2013 to 2022
$3.8M
NEUROVIROLOGY-MOLECULAR BIOLOGYT32NS007321 · NINDS · UNIVERSITY OF COLORADO DENVER · PI GILDEN, DONALD · 1988 to 2014
$2.3M
The Role of Intrathecal Plasma Cell Clones in MS PathogenesisR01NS072141 · NINDS · UNIVERSITY OF COLORADO DENVER · PI OWENS, GREGORY PARKS · 2011 to 2015
$1.3M
NCATS NIH HHS UL1 TR001082NEI NIH HHS EY022936NEI NIH HHS R01 EY022936NIGMS NIH HHS T32 GM008497NINDS NIH HHS NS007321NINDS NIH HHS NS072141NINDS NIH HHS P30 NS048154NINDS NIH HHS R01 NS072141NINDS NIH HHS T32 NS007321
6 · The paper itself

Abstract

B cells are implicated in the etiology of multiple sclerosis (MS). Intrathecal IgG synthesis, cerebrospinal fluid (CSF) oligoclonal bands and lesional IgG deposition suggest a role for antibody-mediated pathology. We examined the binding of IgG1 monoclonal recombinant antibodies (rAbs) derived from MS patient CSF expanded B cell clones to central nervous system (CNS) tissue. MS rAbs displaying CNS binding to mouse and human CNS tissue were further tested for their ability to induce complement-mediated tissue injury in ex vivo spinal cord explant cultures. The staining of CNS tissue, primary human astrocytes and human neurons revealed a measurable bias in MS rAb binding to antigens preferentially expressed on astrocytes and neurons. MS rAbs that recognize myelin-enriched antigens were rarely detected. Both myelin-specific and some astrocyte/neuronal-specific MS rAbs caused significant myelin loss and astrocyte activation when applied to spinal cord explant cultures in the presence of complement. Overall, the intrathecal B cell response in multiple sclerosis binds to both glial and neuronal targets and produces demyelination in spinal cord explant cultures implicating intrathecal IgG in MS pathogenesis.

Indexed as

AdultAnimalsAnimals, Outbred StrainsAntibodies, MonoclonalAstrocytesAutoantibodiesCell Line, TumorCells, CulturedCerebral CortexDemyelinating DiseasesFemaleHumansImmunoglobulin GInduced Pluripotent Stem CellsMice, Inbred C57BLMultiple SclerosisAntibodies, MonoclonalAutoantibodiesImmunoglobulin GRecombinant ProteinsAutoimmunityDemyelinationMonoclonal antibodyMultiple sclerosisNeuroimmunologySpinal cord slice cultures

Identifiers

PMID26511623
PMCPMC4655138
OpenAlexW2206947362

What OpenQuestion holds

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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.