Evidence map›Paper›PMID 36168923›Full record

ArticleBritish journal of haematology2023

Truncated CSF3 receptors induce pro-inflammatory responses in severe congenital neutropenia.

Patricia A Olofsen, Dennis A Bosch, Hans W J de Looper, Paulina M H van Strien, Remco M Hoogenboezem, Onno Roovers, Vincent H J van der Velden, Eric M J Bindels, Emma M De Pater, Ivo P Touw

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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  9. The role of GATA2 in adult hematopoiesis and cell fate determination.Frontiers in cell and developmental biology · 2023
    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

10 authors at 1 institution in 1 country.

Patricia A OlofsenDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0002-6100-9290
Dennis A BoschDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Hans W J de LooperDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Paulina M H van StrienDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Remco M HoogenboezemDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Onno RooversDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Vincent H J van der VeldenDepartment of Immunology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Eric M J BindelsDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Emma M De PaterDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.
Ivo P TouwDepartment of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0002-4773-4074
Erasmus MC · NL

Funding

Daniel den Hoed FoundationKWF Kankerbestrijding EMCR 2013-6080KWF Kankerbestrijding EMCR 2014-6780
6 · The paper itself

Abstract

Severe congenital neutropenia (SCN) patients are prone to develop myelodysplastic syndrome (MDS) or acute myeloid leukaemia (AML). Leukaemic progression of SCN is associated with the early acquisition of CSF3R mutations in haematopoietic progenitor cells (HPCs), which truncate the colony-stimulating factor 3 receptor (CSF3R). These mutant clones may arise years before MDS/AML becomes overt. Introduction and activation of CSF3R truncation mutants in normal HPCs causes a clonally dominant myeloproliferative state in mice treated with CSF3. Paradoxically, in SCN patients receiving CSF3 therapy, clonal dominance of CSF3R mutant clones usually occurs only after the acquisition of additional mutations shortly before frank MDS or AML is diagnosed. To seek an explanation for this discrepancy, we introduced a patient-derived CSF3R-truncating mutation in ELANE-SCN and HAX1-SCN derived and control induced pluripotent stem cells and compared the CSF3 responses of HPCs generated from these lines. In contrast to CSF3R-mutant control HPCs, CSF3R-mutant HPCs from SCN patients do not show increased proliferation but display elevated levels of inflammatory signalling. Thus, activation of the truncated CSF3R in SCN-HPCs does not evoke clonal outgrowth but causes a sustained pro-inflammatory state, which has ramifications for how these CSF3R mutants contribute to the leukaemic transformation of SCN.

Indexed as

Leukemia, Myeloid, AcuteMyelodysplastic SyndromesAnimalsCongenital Bone Marrow Failure SyndromesMiceMutationNeutropeniaCSF3R mutationleukaemiapro-inflammatory signallingsevere congenital neutropenia

Identifiers

PMID36168923
PMCPMC10087386
OpenAlexW4297463314

What OpenQuestion holds

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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.