Evidence map›Paper›PMID 35416319›Full record

ArticleImmunology and cell biology2022

Peripheral B-cell dysregulation is associated with relapse after long-term quiescence in patients with multiple sclerosis.

Felix Marsh-Wakefield, Pierre Juillard, Thomas M Ashhurst, Annette Juillard, Diana Shinko, Givanna H Putri, Mark N Read, Helen M McGuire, Scott N Byrne, Simon Hawke and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Immunology and cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. A unique cytotoxic CD4Clinical & translational immunology · 2023
    Article
  7. Article
  8. Article
  9. Circulating CCR6Clinical & translational immunology · 2022
    Article
  10. 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

11 authors at 1 institution in 1 country.

Felix Marsh-WakefieldVascular Immunology Unit, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.ORCID 0000-0002-6839-7628
Pierre JuillardVascular Immunology Unit, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
Thomas M AshhurstSydney Cytometry Core Research Facility, The University of Sydney, Sydney, NSW, Australia.ORCID 0000-0001-7269-7773
Annette JuillardVascular Immunology Unit, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
Diana ShinkoSydney Cytometry Core Research Facility, The University of Sydney, Sydney, NSW, Australia.
Givanna H PutriSchool of Computer Science, The University of Sydney, Sydney, NSW, Australia.
Mark N ReadSchool of Computer Science, The University of Sydney, Sydney, NSW, Australia.
Helen M McGuireRamaciotti Facility for Human Systems Biology, The University of Sydney, Sydney, NSW, Australia.ORCID 0000-0003-2047-6543
Scott N ByrneSchool of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.ORCID 0000-0003-3029-1710
Simon HawkeVascular Immunology Unit, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
Georges E GrauVascular Immunology Unit, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia.
The University of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B cells play a major role in multiple sclerosis (MS), with many successful therapeutics capable of removing them from circulation. One such therapy, alemtuzumab, is thought to reset the immune system without the need for ongoing therapy in a proportion of patients. The exact cells contributing to disease pathogenesis and quiescence remain to be identified. We utilized mass cytometry to analyze B cells from the blood of patients with relapse-remitting MS (RRMS) before and after alemtuzumab treatment, and during relapse. A complementary RRMS cohort was analyzed by single-cell RNA sequencing. The R package "Spectre" was used to analyze these data, incorporating FlowSOM clustering, sparse partial least squares-discriminant analysis and permutational multivariate analysis of variance. Immunoglobulin (Ig)A

Indexed as

Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingAlemtuzumabChronic DiseaseHumansImmunoglobulin AImmunoglobulin GRecurrenceAlemtuzumabImmunoglobulin AImmunoglobulin GAlemtuzumabB cellsmass cytometrymultiple sclerosis

Identifiers

PMID35416319
PMCPMC9322415
OpenAlexW4223478935

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.