Evidence map›Paper›PMID 29296797›Full record

ArticleBlood advances2017

Patient-derived antibody recognizes a unique CD43 epitope expressed on all AML and has antileukemia activity in mice.

Marijn A Gillissen, Greta de Jong, Martijn Kedde, Etsuko Yasuda, Sophie E Levie, Gemma Moiset, Paul J Hensbergen, Arjen Q Bakker, Koen Wagner, Jullien Villaudy and 3 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 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, 31 citations in OpenAlex.

  1. Review
  2. Sialylated CD43 is a glyco-immune checkpoint for macrophage phagocytosis.bioRxiv : the preprint server for biology · 2025
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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

13 authors at 3 institutions in 1 country.

Marijn A GillissenAIMM Therapeutics, Amsterdam, The Netherlands.
Greta de JongAIMM Therapeutics, Amsterdam, The Netherlands.
Martijn KeddeAIMM Therapeutics, Amsterdam, The Netherlands.
Etsuko YasudaAIMM Therapeutics, Amsterdam, The Netherlands.
Sophie E LevieAIMM Therapeutics, Amsterdam, The Netherlands.
Gemma MoisetAIMM Therapeutics, Amsterdam, The Netherlands.
Paul J HensbergenCenter for Proteomics and Metabolomics, University Medical Center, Leiden, The Netherlands; and.
Arjen Q BakkerAIMM Therapeutics, Amsterdam, The Netherlands.
Koen WagnerAIMM Therapeutics, Amsterdam, The Netherlands.
Jullien VillaudyAIMM Therapeutics, Amsterdam, The Netherlands.
Pauline M van HeldenAIMM Therapeutics, Amsterdam, The Netherlands.
Hergen SpitsAIMM Therapeutics, Amsterdam, The Netherlands.
Mette D HazenbergDepartment of Hematology, Academic Medical Center, Amsterdam, The Netherlands.
AIMM Therapeutics (Netherlands) · NLAcademic Medical Center · NLNetherlands Metabolomics Centre · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy has proven beneficial in many hematologic and nonhematologic malignancies, but immunotherapy for acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) is hampered by the lack of tumor-specific targets. We took advantage of the tumor-immunotherapeutic effect of allogeneic hematopoietic stem cell transplantation and searched the B-cell repertoire of a patient with a lasting and potent graft-versus-AML response for the presence of AML-specific antibodies. We identified an antibody, AT1413, that was of donor origin and that specifically recognizes a novel sialylated epitope on CD43 (CD43s). Strikingly, CD43s is expressed on all World Health Organization 2008 types of AML and MDS. AT1413 induced antibody-dependent cell-mediated cytotoxicity and complement-dependent cytotoxicity of AML cells in vitro. Of note, AT1413 was highly efficacious against AML cells in a humanized mouse model without affecting nonmalignant human myeloid cells, suggesting AT1413 has potential as a therapeutic antibody.

Identifiers

PMID29296797
PMCPMC5728470
OpenAlexW2748393501

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.