Evidence map›Paper›PMID 36997299›Full record

ArticleImmunology and cell biology2023

Mutation of the TGN1412 anti-CD28 monoclonal antibody lower hinge confers specific FcγRIIb binding and retention of super-agonist activity.

Alicia M Chenoweth, Sandra Esparon, Bruce D Wines, Janine Schuurman, Aran F Labrijn, P Mark Hogarth

Open access · hybridAbstract read
In one paragraph

Article in Immunology and cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
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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

6 authors at 2 institutions in 2 countries.

Alicia M ChenowethImmune Therapies Group, Burnet Institute, Melbourne, VIC, Australia.
Sandra EsparonImmune Therapies Group, Burnet Institute, Melbourne, VIC, Australia.
Bruce D WinesImmune Therapies Group, Burnet Institute, Melbourne, VIC, Australia.
Janine SchuurmanGenmab, Utrecht, The Netherlands.
Aran F LabrijnGenmab, Utrecht, The Netherlands.ORCID 0000-0001-9239-8439
P Mark HogarthImmune Therapies Group, Burnet Institute, Melbourne, VIC, Australia.
Burnet Institute · AUGenmab (Netherlands) · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The agonistic action of several immunomodulatory monoclonal antibodies (mAbs) requires both target antigen binding and clustering of this mAb:target complex by the Fcs interacting with Fcγ receptors (FcγRs), in particular FcγRIIb, on neighboring bystander cells. Fc mutations were made in the immunoglobulin G4 (IgG4)-based TGN1412 anti-CD28 mAb to define the role of FcγR interactions in its "super-agonist" activity. The dual mutation, IgG4-ED

Indexed as

Immunoglobulin GReceptors, IgGAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedHumansMutationAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedImmunoglobulin GReceptors, IgGTGN-1412antibody Fc engineeringCD28 super-agonismcytokine release syndromeinhibitory FcRmonoclonal antibody therapeutics

Identifiers

PMID36997299
PMCPMC10952187
OpenAlexW4361243414

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.