Evidence map›Paper›PMID 31748274›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Anti-CD20 therapy depletes activated myelin-specific CD8

Joseph J Sabatino, Michael R Wilson, Peter A Calabresi, Stephen L Hauser, Jonathan P Schneck, Scott S Zamvil

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed, 1 pooled it
4.1field-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

79 citing papers in PubMed, 1 synthesis or guideline pooled it, 109 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Observational
  5. Article
  6. Article
  7. Evolving role of CD8Frontiers in immunology · 2026
    Review
  8. Neuron-reactive KIRNature communications · 2025
    Article
  9. In-Depth Characterization of L1CAMInternational journal of molecular sciences · 2025
    Article
  10. TDP-43 pathology induces CD8bioRxiv : the preprint server for biology · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Current Knowledge about CD3International journal of molecular sciences · 2024
    Review
  17. Article
  18. Review
  19. Ocrelizumab Alters Cytotoxic Lymphocyte Function While Reducing EBV-Specific CD8Neurology(R) neuroimmunology & neuroinflammation · 2024
    Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Joseph J SabatinoDepartment of Neurology, University of California, San Francisco, CA 94158; jsabatino@ucsf.neuroimmunol.org zamvil@ucsf.neuroimmunol.org.ORCID 0000-0002-6804-7441
Michael R WilsonDepartment of Neurology, University of California, San Francisco, CA 94158.ORCID 0000-0002-8705-5084
Peter A CalabresiDepartment of Neurology, Johns Hopkins School of Medicine, Baltimore, MD 21205.ORCID 0000-0002-7776-6472
Stephen L HauserDepartment of Neurology, University of California, San Francisco, CA 94158.
Jonathan P SchneckDepartment of Pathology, Johns Hopkins School of Medicine, Baltimore, MD 21287.
Scott S ZamvilDepartment of Neurology, University of California, San Francisco, CA 94158; jsabatino@ucsf.neuroimmunol.org zamvil@ucsf.neuroimmunol.org.ORCID 0000-0003-2720-9915
University of California, San Francisco · USJohns Hopkins University · US

Funding

The Role of B cells in the Origin and Progression of Multiple SclerosisR35NS111644 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI STEPHEN L HAUSER · 2019 to 2026
$9.1M
NINDS Research Education Programs for Residents and Fellows in Neurology, Neurosurgery, Neuropathology, Neuroradiology and Emergency Medicine (R25)R25NS070680 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JOSEPHSON, SCOTT ANDREW · 2010 to 2023
$6.8M
Mechanisms by which effector T cells modulate endogenous remyelinationR37NS041435 · NINDS · JOHNS HOPKINS UNIVERSITY · PI CALABRESI, PETER A · 2013 to 2019
$3.0M
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
Disease relevance of CD20 expression on T cells in multiple sclerosis patientsR01NS092835 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HAUSER, STEPHEN L · 2015 to 2018
$1.7M
Detection of disease-relevant CD8+ T cells in Multiple SclerosisK08NS107619 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SABATINO, JOSEPH JOHN · 2019 to 2023
$1.0M
BD FACSAria II Flow CytometerS10RR028962 · NCRR · J. DAVID GLADSTONE INSTITUTES · PI CAVROIS, MARIELLE · 2011 to 2011
$544k
Influence of NMO gut microbiota on CNS autoantigen-specific T cell responsesR21NS108159 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZAMVIL, SCOTT S · 2018 to 2019
$451k
Single cell RNA-Seq and clonal analysis of CD8+ T cells in MSR21AI142186 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZAMVIL, SCOTT S · 2019 to 2020
$443k
NCRR NIH HHS S10 RR028962NIAID NIH HHS R01 AI131624NIAID NIH HHS R21 AI142186NINDS NIH HHS K08 NS107619NINDS NIH HHS R01 NS092835NINDS NIH HHS R21 NS108159NINDS NIH HHS R25 NS070680NINDS NIH HHS R35 NS111644NINDS NIH HHS R37 NS041435
6 · The paper itself

Abstract

CD8

Indexed as

Antigens, CD20CD8-Positive T-LymphocytesMultiple SclerosisAdolescentAdultAntibodies, MonoclonalCells, CulturedFemaleHumansMaleMiddle AgedMyelin ProteinsYoung AdultAntibodies, MonoclonalAntigens, CD20Myelin Proteinsanti-CD20 therapyCD8+ T cellsmultiple sclerosismyelin antigen

Identifiers

PMID31748274
PMCPMC6926057
OpenAlexW2989833866

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.