Evidence map›Paper›PMID 37635627›Full record

ArticleEMBO molecular medicine2023

M-CSF directs myeloid and NK cell differentiation to protect from CMV after hematopoietic cell transplantation.

Prashanth K Kandalla, Julien Subburayalu, Clément Cocita, Bérengère de Laval, Elena Tomasello, Johanna Iacono, Jessica Nitsche, Maria M Canali, Wilfried Cathou, Gilles Bessou and 9 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 18 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 2 countries.

Prashanth K Kandalla *Center for Regenerative Therapies Dresden (CRTD), Technical University Dresden, Dresden, Germany.
Julien Subburayalu *Center for Regenerative Therapies Dresden (CRTD), Technical University Dresden, Dresden, Germany.ORCID 0000-0001-9243-0558
Clément Cocita *Aix Marseille University, CNRS, INSERM, CIML, Marseille, France.
Bérengère de Laval *Aix Marseille University, CNRS, INSERM, CIML, Marseille, France.
Elena TomaselloAix Marseille University, CNRS, INSERM, CIML, Marseille, France.
Johanna IaconoAix Marseille University, CNRS, INSERM, CIML, Marseille, France.
Jessica NitscheCenter for Regenerative Therapies Dresden (CRTD), Technical University Dresden, Dresden, Germany.ORCID 0009-0002-7267-7857
Maria M CanaliAix Marseille University, CNRS, INSERM, CIML, Marseille, France.ORCID 0000-0002-5787-7909
Wilfried CathouAix Marseille University, CNRS, INSERM, CIML, Marseille, France.
Gilles BessouAix Marseille University, CNRS, INSERM, CIML, Marseille, France.
Noushin Mossadegh-KellerAix Marseille University, CNRS, INSERM, CIML, Marseille, France.ORCID 0000-0002-7088-3676
Caroline HuberAix Marseille University, CNRS, INSERM, CIML, Marseille, France.
Guy MouchiroudInstitut NeuroMyoGene, UMR CNRS 5310, INSERM, Lyon, France.ORCID 0000-0002-7823-7353
Roland P BouretteCNRS, INSERM, CHU Lille, University Lille, UMR9020-U1277 - CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, Lille, France.ORCID 0000-0003-2074-4878
Marie-France GrassetCNRS UMR5534, Claude Bernard Lyon 1 University, Villeurbanne, France.
Martin BornhäuserCenter for Regenerative Therapies Dresden (CRTD), Technical University Dresden, Dresden, Germany.ORCID 0000-0002-5916-3029
Sandrine SarrazinCenter for Regenerative Therapies Dresden (CRTD), Technical University Dresden, Dresden, Germany.ORCID 0000-0001-6435-0913
Marc Dalod *Aix Marseille University, CNRS, INSERM, CIML, Marseille, France.ORCID 0000-0002-6436-7966
Michael H Sieweke *Center for Regenerative Therapies Dresden (CRTD), Technical University Dresden, Dresden, Germany.ORCID 0000-0002-3228-9537
Centre National de la Recherche Scientifique · FRNational Center for Tumor Diseases · DETechnische Universität Dresden · DEUniversité Claude Bernard Lyon 1 · FRUniversity Hospital Carl Gustav Carus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapies reconstituting autologous antiviral immunocompetence may represent an important prophylaxis and treatment for immunosuppressed individuals. Following hematopoietic cell transplantation (HCT), patients are susceptible to Herpesviridae including cytomegalovirus (CMV). We show in a murine model of HCT that macrophage colony-stimulating factor (M-CSF) promoted rapid antiviral activity and protection from viremia caused by murine CMV. M-CSF given at transplantation stimulated sequential myeloid and natural killer (NK) cell differentiation culminating in increased NK cell numbers, production of granzyme B and interferon-γ. This depended upon M-CSF-induced myelopoiesis leading to IL15Rα-mediated presentation of IL-15 on monocytes, augmented by type I interferons from plasmacytoid dendritic cells. Demonstrating relevance to human HCT, M-CSF induced myelomonocytic IL15Rα expression and numbers of functional NK cells in G-CSF-mobilized hematopoietic stem and progenitor cells. Together, M-CSF-induced myelopoiesis triggered an integrated differentiation of myeloid and NK cells to protect HCT recipients from CMV. Thus, our results identify a rationale for the therapeutic use of M-CSF to rapidly reconstitute antiviral activity in immunocompromised individuals, which may provide a general paradigm to boost innate antiviral immunocompetence using host-directed therapies.

Indexed as

Cytomegalovirus InfectionsHematopoietic Stem Cell TransplantationAnimalsAntiviral AgentsCell DifferentiationCytomegalovirusHematopoiesisHumansMacrophage Colony-Stimulating FactorMiceAntiviral AgentsMacrophage Colony-Stimulating FactorCMV (prophylaxis)HCThost-directed therapyM-CSF (CSF-1)NK cell

Identifiers

PMID37635627
PMCPMC10630876
OpenAlexW4386208899

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.