Evidence map›Paper›PMID 28848067›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Aiolos Overexpression in Systemic Lupus Erythematosus B Cell Subtypes and BAFF-Induced Memory B Cell Differentiation Are Reduced by CC-220 Modulation of Cereblon Activity.

Yumi Nakayama, Jolanta Kosek, Lori Capone, Eun Mi Hur, Peter H Schafer, Garth E Ringheim

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03161483 (A PHASE 2, MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF CC-220 IN SUBJECTS WITH ACTIVE SYSTEMIC LUPUS ERYTHEMATOSUS), which is not on this map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
4.2field-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.

NCT03161483 phase2completednot on this map

A phase 2, multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of cc-220 in subjects with active systemic lupus erythematosus

TypeinterventionalSponsorCelgeneRan2017 to 2021Enrolled289ConditionsLupus Erythematosus, SystemicArmsCC-220, Placebo
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Review
  9. Neddylation Regulation of Immune Responses.Research (Washington, D.C.) · 2023
    Review
  10. NF-kB's contribution to B cell fate decisions.Frontiers in immunology · 2023
    Review
  11. Review
  12. Article
  13. B Cell Aberrance in Lupus: the Ringleader and the Solution.Clinical reviews in allergy & immunology · 2022
    Review
  14. Cereblon: promise and challenges for combating human diseases.Pflugers Archiv : European journal of physiology · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

6 authors.

Yumi NakayamaInflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ 07901.
Jolanta KosekInflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ 07901.
Lori CaponeInflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ 07901.
Eun Mi HurInflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ 07901.ORCID 0000-0003-1179-6625
Peter H SchaferInflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ 07901.
Garth E RingheimInflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ 07901 gringheim@celgene.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BAFF is a B cell survival and maturation factor implicated in the pathogenesis of systemic lupus erythematosus (SLE). In this in vitro study, we describe that soluble BAFF in combination with IL-2 and IL-21 is a T cell contact-independent inducer of human B cell proliferation, plasmablast differentiation, and IgG secretion from circulating CD27

Indexed as

Immunologic MemoryAdaptor Proteins, Signal TransducingAntibody FormationB-Cell Activating FactorB-Lymphocyte SubsetsCD40 LigandCell DifferentiationHeterocyclic Compounds, 4 or More RingsHumansIkaros Transcription FactorInterleukin-2Interleukin-21InterleukinsLupus Erythematosus, SystemicMorpholinesPeptide HydrolasesAdaptor Proteins, Signal TransducingB-Cell Activating FactorCD40 LigandCRBN protein, humanHeterocyclic Compounds, 4 or More RingsiberdomideIkaros Transcription FactorIKZF1 protein, humanIKZF3 protein, humanInterleukin-2Interleukin-21InterleukinsMorpholinesPeptide HydrolasesPhthalimidesPiperidonesTNFSF13B protein, humanTumor Necrosis Factor Receptor Superfamily, Member 7Ubiquitin-Protein Ligases

Identifiers

PMID28848067
PMCPMC5602157
OpenAlexW2752652435

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.