Evidence map›Paper›PMID 24828435›Full record

Trial reportmAbs

Suppression of innate and adaptive B cell activation pathways by antibody coengagement of FcγRIIb and CD19.

Dániel Szili, Marcell Cserhalmi, Zsuzsanna Bankó, György Nagy, David E Szymkowski, Gabriella Sármay

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in mAbs. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
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  11. Review
  12. Article
  13. Review
  14. Rituximab resistance in ITP and beyond.Frontiers in immunology · 2023
    Review
  15. Review
  16. IMGTAntibodies (Basel, Switzerland) · 2022
    Article
  17. B Cell Aberrance in Lupus: the Ringleader and the Solution.Clinical reviews in allergy & immunology · 2022
    Review
  18. Review
  19. Inhibition of B cell activation followingJournal of translational autoimmunity · 2021
    Article
  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 at 3 institutions in 4 countries.

Dániel SziliDepartment of Immunology; Eötvös Loránd University; Budapest, Hungary.
Marcell CserhalmiDepartment of Immunology; Eötvös Loránd University; Budapest, Hungary.
Zsuzsanna BankóDepartment of Immunology; Eötvös Loránd University; Budapest, Hungary.
György NagyDepartment of Rheumatology; Polyclinic of the Hospitaller Brothers of St. John of God; Budapest, Hungary.
David E Szymkowski
Gabriella Sármay
Eötvös Loránd University · HUHospital of the Brothers of St. John of God · ATXencor (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Fc receptor (FcγRIIb) inhibits B cell responses when coengaged with B cell receptor (BCR), and has become a target for new autoimmune disease therapeutics. For example, BCR and FcγRIIb coengagement via the Fc-engineered anti-CD19 XmAb5871 suppresses humoral immune responses. We now assess effects of XmAb5871 on other activation pathways, including the pathogen-associated molecular pattern receptor, TLR9. Since TLR9 signaling is implicated in autoimmune diseases, we asked if XmAb5871 could inhibit TLR9 costimulation. We show that XmAb5871 decreases ERK and AKT activation, cell proliferation, cytokine, and IgG production induced by BCR and/or TLR9 signals. XmAb5871 also inhibited differentiation of citrullinated peptide-specific plasma cells from rheumatoid arthritis patients. XmAb5871 may therefore have potential to suppress pathogenic B cells in autoimmune diseases.

Indexed as

Antigens, CD19AdultAgedAntibodies, MonoclonalB-LymphocytesCell ProliferationCytokinesFemaleHumansImmunity, InnateImmunoglobulin GImmunosuppressive AgentsLymphocyte ActivationMaleMAP Kinase Signaling SystemMiddle AgedAntibodies, MonoclonalAntigens, CD19CytokinesFCGR2B protein, humanImmunoglobulin GImmunosuppressive AgentsReceptors, Antigen, B-CellReceptors, IgGTLR9 protein, humanToll-Like Receptor 9antibody therapyautoimmuneB cellFc-engineeredhumanized antibodyrheumatoid arthritissignalingTLR

Identifiers

PMID24828435
PMCPMC4171032
OpenAlexW2059213205

What OpenQuestion holds

Textmetadata
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.