Evidence map›Paper›PMID 19557869›Full record

ArticleAnnals of neurology2009

Antibodies produced by clonally expanded plasma cells in multiple sclerosis cerebrospinal fluid.

Gregory P Owens, Jeffrey L Bennett, Hans Lassmann, Kevin C O'Connor, Alanna M Ritchie, Andrew Shearer, Chiwah Lam, Xiaoli Yu, Marius Birlea, Cecily DuPree and 4 more

Abstract readComparative Study
In one paragraph

Article in Annals of neurology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed, 1 pooled it
–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

103 citing papers in PubMed, 1 synthesis or guideline pooled it.

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43 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Gregory P OwensDepartment of Neurology, University of Colorado Denver School of Medicine, Denver, CO 80045, USA.
Jeffrey L Bennett
Hans Lassmann
Kevin C O'Connor
Alanna M Ritchie
Andrew Shearer
Chiwah Lam
Xiaoli Yu
Marius Birlea
Cecily DuPree
R Anthony Williamson
David A Hafler
Mark P Burgoon
Don Gilden

Funding

Varicella Zoster Virus Latency in Human GangliaP01NS032623 · NINDS · UNIVERSITY OF COLORADO DENVER · PI MAHLAINGAM, RAVI · 1993 to 2008
$12.3M
Antigen Identification in Inflammatory CNS DiseaseR01NS041549 · NINDS · UNIVERSITY OF COLORADO DENVER · PI BURGOON, MARK P · 2002 to 2014
$3.1M
Antigen Identification in Occult ChorioretinopathiesR03EY014573 · NEI · UNIVERSITY OF COLORADO DENVER · PI BENNETT, JEFFREY L · 2004 to 2006
$458k
NEI NIH HHS EY014573NEI NIH HHS R03 EY014573NINDS NIH HHS NS041549NINDS NIH HHS NS32623NINDS NIH HHS P01 NS032623NINDS NIH HHS R01 NS041549
6 · The paper itself

Abstract

objectiveIntrathecal IgG synthesis, persistence of bands of oligoclonal IgG, and memory B-cell clonal expansion are well-characterized features of the humoral response in multiple sclerosis (MS). Nevertheless, the target antigen of this response remains enigmatic.

methodsWe produced 53 different human IgG1 monoclonal recombinant antibodies (rAbs) by coexpressing paired heavy- and light-chain variable region sequences of 51 plasma cell clones and 2 B-lymphocyte clones from MS cerebrospinal fluid in human tissue culture cells. Chimeric control rAbs were generated from anti-myelin hybridomas in which murine variable region sequences were fused to human constant region sequences. Purified rAbs were exhaustively assayed for reactivity against myelin basic protein, proteolipid protein, and myelin oligodendrocyte glycoprotein by immunostaining of transfected cells expressing individual myelin proteins, by protein immunoblotting, and by immunostaining of human brain tissue sections.

resultsWhereas humanized control rAbs derived from anti-myelin hybridomas and anti-myelin monoclonal antibodies readily detected myelin antigens in multiple immunoassays, none of the rAbs derived from MS cerebrospinal fluid displayed immunoreactivity to the three myelin antigens tested. Immunocytochemical analysis of tissue sections from MS and control brain demonstrated only weak staining with a few rAbs against nuclei or cytoplasmic granules in neurons, glia, and inflammatory cells.

interpretationThe oligoclonal B-cell response in MS cerebrospinal fluid is not targeted to the well-characterized myelin antigens myelin basic protein, proteolipid protein, or myelin oligodendrocyte glycoprotein.

Indexed as

Cell ProliferationAnimalsAntibodies, MonoclonalB-Lymphocyte SubsetsCell LineClone CellsHumansImmunoglobulin GMiceMice, Inbred BALB CMultiple SclerosisPlasma CellsRecombinant ProteinsAntibodies, MonoclonalImmunoglobulin GRecombinant Proteins

Identifiers

PMID19557869
PMCPMC2843543

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Registered trials

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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.