Evidence map›Paper›PMID 28506291›Full record

ArticleArthritis research & therapy2017

Targeting CD22 with the monoclonal antibody epratuzumab modulates human B-cell maturation and cytokine production in response to Toll-like receptor 7 (TLR7) and B-cell receptor (BCR) signaling.

Natalia V Giltiay, Geraldine L Shu, Anthony Shock, Edward A Clark

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

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  10. Targeted Therapy for Primary Sjögren's Syndrome: Where are We Now?BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2021
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  12. Leptin: an unappreciated key player in SLE.Clinical rheumatology · 2020
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  14. HighFrontiers in immunology · 2019
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. miR-155 Regulates IL-10-Producing CD24Frontiers in immunology · 2017
    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

4 authors at 2 institutions in 2 countries.

Natalia V GiltiayDivision of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, 98109, USA. giltiayn@uw.edu.
Geraldine L ShuDepartment of Immunology, University of Washington, Seattle, WA, 98109, USA.
Anthony ShockUCB Celltech, Slough, UK.
Edward A ClarkDivision of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, 98109, USA.
University of Washington · USUCB Pharma (United Kingdom) · GB

Funding

FDRC1 AND FOLLICULAR DENDRITIC CELL SIGNALING PATHWAYSR37AI044257 · NIAID · UNIVERSITY OF WASHINGTON · PI CLARK, EDWARD A · 2004 to 2013
$4.0M
Role of B cell activating factor (BAFF) in B cell responses and autoimmunityR01AI044257 · NIAID · UNIVERSITY OF WASHINGTON · PI GILTIAY, NATALIA V · 1999 to 2020
$3.7M
NIAID NIH HHS R01 AI044257NIAID NIH HHS R37 AI044257
6 · The paper itself

Abstract

backgroundAbnormal B-cell activation is implicated in the pathogenesis of autoimmune diseases, including systemic lupus erythematosus (SLE). The B-cell surface molecule CD22, which regulates activation through the B-cell receptor (BCR), is a potential target for inhibiting pathogenic B cells; however, the regulatory functions of CD22 remain poorly understood. In this study, we determined how targeting of CD22 with epratuzumab (Emab), a humanized anti-CD22 IgG1 monoclonal antibody, affects the activation of human B-cell subsets in response to Toll-like receptor 7 (TLR7) and BCR engagement.

methodsB-cell subsets were isolated from human tonsils and stimulated with F(ab')

resultsPretreatment of phenotypically naïve CD19

conclusionsEmab can both regulate cytokine expression and block Blimp1-dependent B-cell differentiation, although the effects of Emab may depend on the stage of B-cell development or activation. In addition, Emab inhibits the activation of CD27

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedB-LymphocytesCells, CulturedCell SurvivalCytokinesDrug Delivery SystemsHumansPositive Regulatory Domain I-Binding Factor 1Sialic Acid Binding Ig-like Lectin 2Toll-Like Receptor 7Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedCD22 protein, humanCytokinesepratuzumabPositive Regulatory Domain I-Binding Factor 1PRDM1 protein, humanSialic Acid Binding Ig-like Lectin 2TLR7 protein, humanToll-Like Receptor 7AntibodiesB cellsB-cell targeted therapyCD22EpratuzumabIL-10IL-6Systemic lupus erythematosusTLR7

Identifiers

PMID28506291
PMCPMC5433084
OpenAlexW2614577379

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.