Evidence map›Paper›PMID 36635380›Full record

ArticleNature biotechnology2023

Control of acute myeloid leukemia by a trifunctional NKp46-CD16a-NK cell engager targeting CD123.

Laurent Gauthier, Angela Virone-Oddos, Jochen Beninga, Benjamin Rossi, Céline Nicolazzi, Céline Amara, Audrey Blanchard-Alvarez, Nicolas Gourdin, Jacqueline Courta, Alexandra Basset and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Nature biotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
16.1field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 98 citations in OpenAlex.

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  15. Engineering antibody-drug conjugates targeting an adhesion GPCR, CD97.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  16. Nanoscale restructuring of the immune synapse with an engager enhances NK cell function.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  17. Article
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  20. Killing the killers: Natural killer cell therapy targeting glioma stem cells in high-grade glioma.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review

2 more citing papers are in PubMed but not listed here.

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

19 authors at 4 institutions in 2 countries.

Laurent Gauthier *Innate Pharma, Marseille, France. laurent.gauthier@innate-pharma.fr.ORCID http://orcid.org/0000-0003-3225-4825
Angela Virone-Oddos *Sanofi Immuno-Oncology Research, Vitry sur-Seine, France. Angela.Virone-Oddos@sanofi.com.ORCID http://orcid.org/0000-0002-4511-0612
Jochen BeningaSanofi Large Molecules Research, Frankfurt, Germany.
Benjamin RossiInnate Pharma, Marseille, France.
Céline NicolazziSanofi Immuno-Oncology Research, Vitry sur-Seine, France.
Céline AmaraSanofi Drug Metabolism and Pharmacokinetics, Chilly Mazarin, France.
Audrey Blanchard-AlvarezInnate Pharma, Marseille, France.
Nicolas GourdinInnate Pharma, Marseille, France.
Jacqueline CourtaSanofi TMED Biomarkers and Clinical Bioanalysis, Chilly Mazarin, France.
Alexandra BassetSanofi Preclinical Safety, Chilly Mazarin, France.
Magali AgnelSanofi Global Project Management, Vitry sur-Seine, France.
Franceline GuillotInnate Pharma, Marseille, France.
Gwendoline GrondinInnate Pharma, Marseille, France.
Hélène BonnevauxSanofi Immuno-Oncology Research, Vitry sur-Seine, France.ORCID http://orcid.org/0000-0002-4491-669X
Anne-Laure BauchetSanofi Global Project Management, Vitry sur-Seine, France.
Ariane MorelInnate Pharma, Marseille, France.
Yannis MorelInnate Pharma, Marseille, France.
Marielle ChironSanofi Immuno-Oncology Research, Vitry sur-Seine, France.
Eric VivierInnate Pharma, Marseille, France. eric.vivier@innate-pharma.fr.ORCID http://orcid.org/0000-0001-7022-8287
Sanofi (France) · FRInnate Pharma (France) · FRCentre National de la Recherche Scientifique · FRSanofi (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD123, the alpha chain of the IL-3 receptor, is an attractive target for acute myeloid leukemia (AML) treatment. However, cytotoxic antibodies or T cell engagers targeting CD123 had insufficient efficacy or safety in clinical trials. We show that expression of CD64, the high-affinity receptor for human IgG, on AML blasts confers resistance to anti-CD123 antibody-dependent cell cytotoxicity (ADCC) in vitro. We engineer a trifunctional natural killer cell engager (NKCE) that targets CD123 on AML blasts and NKp46 and CD16a on NK cells (CD123-NKCE). CD123-NKCE has potent antitumor activity against primary AML blasts regardless of CD64 expression and induces NK cell activation and cytokine secretion only in the presence of AML cells. Its antitumor activity in a mouse CD123

Indexed as

Leukemia, Myeloid, AcuteAnimalsAntibody-Dependent Cell CytotoxicityCytokinesHumansInterleukin-3 Receptor alpha SubunitKiller Cells, NaturalMiceT-LymphocytesCytokinesInterleukin-3 Receptor alpha Subunit

Identifiers

PMID36635380
PMCPMC10497414
OpenAlexW4315707363

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.