Evidence map›Paper›PMID 30194232›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Functional characterization of reappearing B cells after anti-CD20 treatment of CNS autoimmune disease.

Darius Häusler, Silke Häusser-Kinzel, Linda Feldmann, Sebastian Torke, Gildas Lepennetier, Claude C A Bernard, Scott S Zamvil, Wolfgang Brück, Klaus Lehmann-Horn, Martin S Weber

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

67 citing papers in PubMed, 1 synthesis or guideline pooled it, 105 citations in OpenAlex.

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

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

10 authors at 4 institutions in 3 countries.

Darius HäuslerInstitute of Neuropathology, University Medical Center, 37099 Göttingen, Germany.
Silke Häusser-KinzelInstitute of Neuropathology, University Medical Center, 37099 Göttingen, Germany.
Linda FeldmannInstitute of Neuropathology, University Medical Center, 37099 Göttingen, Germany.
Sebastian TorkeInstitute of Neuropathology, University Medical Center, 37099 Göttingen, Germany.
Gildas LepennetierDepartment of Neurology, Klinikum rechts der Isar, Technische Universität München, 81675 Munich, Germany.ORCID 0000-0002-1899-3149
Claude C A BernardMonash Regenerative Medicine Institute, Monash University, 3800 Melbourne, Australia.
Scott S ZamvilDepartment of Neurology, University of California, San Francisco, CA 94158.
Wolfgang BrückInstitute of Neuropathology, University Medical Center, 37099 Göttingen, Germany.
Klaus Lehmann-HornDepartment of Neurology, Klinikum rechts der Isar, Technische Universität München, 81675 Munich, Germany.
Martin S WeberInstitute of Neuropathology, University Medical Center, 37099 Göttingen, Germany; martin.weber@med.uni-goettingen.de.
University of Göttingen · DETUM Klinikum · DEAustralian Regenerative Medicine Institute · AUUniversity of California, San Francisco · US

Funding

Repertoire selection of AQP4-specific T cells that cause CNS autoimmunediseaseR01AI131624 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZAMVIL, SCOTT S · 2019 to 2023
$2.2M
NIAID NIH HHS R01 AI131624
6 · The paper itself

Abstract

The anti-CD20 antibody ocrelizumab, approved for treatment of multiple sclerosis, leads to rapid elimination of B cells from the blood. The extent of B cell depletion and kinetics of their recovery in different immune compartments is largely unknown. Here, we studied how anti-CD20 treatment influences B cells in bone marrow, blood, lymph nodes, and spleen in models of experimental autoimmune encephalomyelitis (EAE). Anti-CD20 reduced mature B cells in all compartments examined, although a subpopulation of antigen-experienced B cells persisted in splenic follicles. Upon treatment cessation, CD20

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CD20B-LymphocytesBone Marrow CellsEncephalomyelitis, Autoimmune, ExperimentalLymph NodesMiceMice, Inbred C57BLMyelin SheathSpleenAntibodies, MonoclonalAntigens, CD20anti-CD20B cell recoveryexperimental autoimmune encephalomyelitismultiple sclerosissecondary lymphoid organ

Identifiers

PMID30194232
PMCPMC6166805
OpenAlexW2892267648

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.