Evidence map›Paper›PMID 38857395›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Engineering an inducible leukemia-associated fusion protein enables large-scale ex vivo production of functional human phagocytes.

Roland Windisch, Sarah Soliman, Adrian Hoffmann, Linping Chen-Wichmann, Anna Danese, Sebastian Vosberg, Jimena Bravo, Sebastian Lutz, Christian Kellner, Alexander Fischer and 18 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Engineering an inducible leukemia-associated fusion protein enables large-scale ex vivo production of functional human phagocytes.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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

28 authors.

Roland WindischDivision of Transfusion Medicine, Cell Therapeutics and Haemostaseology, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.ORCID 0000-0003-1294-5151
Sarah SolimanDivision of Transfusion Medicine, Cell Therapeutics and Haemostaseology, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Adrian HoffmannVascular Biology, Institute for Stroke and Dementia Research, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Linping Chen-WichmannDivision of Transfusion Medicine, Cell Therapeutics and Haemostaseology, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.ORCID 0009-0003-8439-8107
Anna DaneseBiomedical Center, Department of Physiological Genomics, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Sebastian VosbergDepartment of Medicine III, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.ORCID 0000-0002-8464-1483
Jimena BravoGeorg-Speyer-Haus, Institute for Tumor Biology and Experimental Therapy, Frankfurt am Main 60596, Germany.
Sebastian LutzDivision of Transfusion Medicine, Cell Therapeutics and Haemostaseology, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Christian KellnerDivision of Transfusion Medicine, Cell Therapeutics and Haemostaseology, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.ORCID 0000-0002-2562-6902
Alexander FischerDepartment of Internal Medicine III, University Hospital Regensburg, Regensburg 93053, Germany.ORCID 0000-0001-8876-5566
Claudia GebhardLeibniz Institute for Immunotherapy, Regensburg 93053, Germany.ORCID 0000-0002-5459-8381
Enric Redondo MonteDepartment of Medicine III, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Luise HartmannDepartment of Medicine III, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Stephanie SchneiderDepartment of Medicine III, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Fabian BeierDepartment of Hematology, Oncology, Hemostaseology and Stem Cell Transplantation, Medical Faculty University Hospital Aachen, Rheinisch-Westfälische Technische Hochschule Aachen, Aachen 52074, Germany.ORCID 0000-0002-3718-8217
Carolin Dorothea StroblDepartment of Medicine III, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.ORCID 0000-0003-2257-6281
Oliver WeigertDepartment of Medicine III, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.ORCID 0000-0002-0987-7373
Matthias PeippDivision of Antibody-Based Immunotherapy, Department of Medicine II, Christian Albrechts University of Kiel, Kiel 24105, Germany.
Michael SchündelnPediatric Hematology and Oncology, Department of Pediatrics III, University Hospital Essen and the University of Duisburg-Essen, Essen 45147, Germany.ORCID 0000-0001-7495-9060
Stefan H StrickerBiomedical Center, Department of Physiological Genomics, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Michael RehliDepartment of Internal Medicine III, University Hospital Regensburg, Regensburg 93053, Germany.ORCID 0000-0003-3992-932X
Jürgen BernhagenVascular Biology, Institute for Stroke and Dementia Research, Ludwig-Maximilians-Universität München, Munich 81377, Germany.ORCID 0000-0003-2996-2652
Andreas HumpeDivision of Transfusion Medicine, Cell Therapeutics and Haemostaseology, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.
Hannes KlumpInstitute for Transfusion Medicine, University Hospital Essen, Essen 45147, Germany.ORCID 0000-0003-3536-1212
Christian BrendelDivision of Pediatric Hematology/Oncology, Boston Children's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115.ORCID 0000-0003-4081-4351
Daniela S KrauseGeorg-Speyer-Haus, Institute for Tumor Biology and Experimental Therapy, Frankfurt am Main 60596, Germany.ORCID 0000-0003-3603-1119
Philipp A Greif *Department of Medicine III, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.ORCID 0000-0002-3744-7936
Christian Wichmann *Division of Transfusion Medicine, Cell Therapeutics and Haemostaseology, University Hospital, Ludwig-Maximilians-Universität München, Munich 81377, Germany.

Funding

Deutsche Forschungsgemeinschaft (DFG) DFG STR 1385/5-1Deutsche Forschungsgemeinschaft (DFG) SFB1123-A3DFG under Germany's Excellence Strategy within the framework of the Munich Cluster for Systems Neurology EXC 2145 SyNergy-ID 390857198Friedrich-Baur-Stiftung (Friedrich Baur Stiftung) FB 20/17Friedrich-Baur-Stiftung (Friedrich Baur Stiftung) FB 25/16Friedrich-Baur-Stiftung (Friedrich Baur Stiftung) FB 72/20José Carreras Leukämie-Stiftung (DJCLS) DJCLS 05 FN/2019Metiphys programMunich Clinician Scientist ProgramVolkswagen Foundation (VolkswagenStiftung) 97103Wilhelm Sander-Stiftung (Wilhelm Sander Foundation) 2014.162.2Wilhelm Sander-Stiftung (Wilhelm Sander Foundation) 2014.162.3
6 · The paper itself

Abstract

Ex vivo expansion of human CD34+ hematopoietic stem and progenitor cells remains a challenge due to rapid differentiation after detachment from the bone marrow niche. In this study, we assessed the capacity of an inducible fusion protein to enable sustained ex vivo proliferation of hematopoietic precursors and their capacity to differentiate into functional phagocytes. We fused the coding sequences of an FK506-Binding Protein 12 (FKBP12)-derived destabilization domain (DD) to the myeloid/lymphoid lineage leukemia/eleven nineteen leukemia (MLL-ENL) fusion gene to generate the fusion protein DD-MLL-ENL and retrovirally expressed the protein switch in human CD34+ progenitors. Using Shield1, a chemical inhibitor of DD fusion protein degradation, we established large-scale and long-term expansion of late monocytic precursors. Upon Shield1 removal, the cells lost self-renewal capacity and spontaneously differentiated, even after 2.5 y of continuous ex vivo expansion. In the absence of Shield1, stimulation with IFN-γ, LPS, and GM-CSF triggered terminal differentiation. Gene expression analysis of the obtained phagocytes revealed marked similarity with naïve monocytes. In functional assays, the novel phagocytes migrated toward CCL2, attached to VCAM-1 under shear stress, produced reactive oxygen species, and engulfed bacterial particles, cellular particles, and apoptotic cells. Finally, we demonstrated Fcγ receptor recognition and phagocytosis of opsonized lymphoma cells in an antibody-dependent manner. Overall, we have established an engineered protein that, as a single factor, is useful for large-scale ex vivo production of human phagocytes. Such adjustable proteins have the potential to be applied as molecular tools to produce functional immune cells for experimental cell-based approaches.

Indexed as

Cell DifferentiationPhagocytesHematopoietic Stem CellsHumansLeukemiaMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionPhagocytosisProtein EngineeringRecombinant Fusion ProteinsMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionRecombinant Fusion ProteinsCD34+cellular differentiationhuman blood progenitorsmacrophagesMLL1

Identifiers

PMID38857395
PMCPMC11194515

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