Evidence map›Paper›PMID 27059652›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2016

Checkpoints for Autoreactive B Cells in the Peripheral Blood of Lupus Patients Assessed by Flow Cytometry.

Susan Malkiel, Venkatesh Jeganathan, Stacey Wolfson, Nataly Manjarrez Orduño, Emiliano Marasco, Cynthia Aranow, Meggan Mackay, Peter K Gregersen, Betty Diamond

Open access · greenAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 80 citations in OpenAlex.

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  11. IgDPathogens (Basel, Switzerland) · 2024
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  13. Increased development of T-betClinical immunology (Orlando, Fla.) · 2023
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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

9 authors at 2 institutions in 1 country.

Susan Malkiel
Venkatesh Jeganathan
Stacey Wolfson
Nataly Manjarrez Orduño
Emiliano Marasco
Cynthia AranowFeinstein Institute for Medical Research, Northwell Health, Manhasset, New York.
Meggan MackayFeinstein Institute for Medical Research, Northwell Health, Manhasset, New York.
Peter K GregersenFeinstein Institute for Medical Research, Northwell Health, Manhasset, New York.
Betty DiamondFeinstein Institute for Medical Research, Northwell Health, Manhasset, New York.
Feinstein Institute for Medical Research · USNorthwell Health · US

Funding

The Monoclonal Antibody and Reagent CoreP01AI073693 · NIAID · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI Czeslawa Helena Kowal · 2008 to 2026
$45.8M
Toward a new approach to SLE therapyR01AR057084 · NIAMS · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI DIAMOND, BETTY · 2010 to 2014
$1.8M
NIAID NIH HHS P01 AI073693NIAMS NIH HHS R01 AR057084
6 · The paper itself

Abstract

objectiveAntinuclear antibodies (ANAs) are diagnostic in several autoimmune disorders, yet the failure to achieve B cell tolerance in these diseases is still poorly understood. Although secreted ANAs detected by an indirect immunofluorescence assay are the gold standard for autoreactivity, there has been no convenient assay with which to measure the frequency of circulating B cells that recognize nuclear antigens (ANA+ B cells) in patients. The aim of this study was to generate an assay to easily identify these B cells and to examine its utility in a study of autoreactive B cells in systemic lupus erythematosus (SLE).

methodsWe developed and validated a novel flow cytometry-based assay that identifies ANA+ B cells using biotinylated nuclear extracts, and utilized it to examine B cell tolerance checkpoints in peripheral blood mononuclear cells obtained from SLE patients and healthy controls.

resultsWe observed progressive selection against ANA+ B cells as they matured from transitional to naive to CD27+IgD- and CD27+IgD+ memory cells in both healthy subjects and SLE patients; however, ANA+ naive B cells in SLE patients were not anergized to the same extent as in healthy individuals. We also showed that anergy induction is restored in SLE patients treated with belimumab, an inhibitor of BAFF.

conclusionThis assay will enable studies of large populations to identify potential genetic or environmental factors affecting B cell tolerance checkpoints in healthy subjects and patients with autoimmune disease and permit monitoring of the B cell response to therapeutic interventions.

Indexed as

AdultB-LymphocytesFemaleFlow CytometryHumansImmune ToleranceLupus Erythematosus, SystemicMaleMiddle Aged

Identifiers

PMID27059652
PMCPMC5523861
OpenAlexW2339788350

What OpenQuestion holds

Textmetadata
LicenceTDM
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.