Evidence map›Paper›PMID 36901798›Full record

ArticleInternational journal of molecular sciences2023

Co-Transplantation of Barcoded Lymphoid-Primed Multipotent (LMPP) and Common Lymphocyte (CLP) Progenitors Reveals a Major Contribution of LMPP to the Lymphoid Lineage.

Victoria Michaels, Smahane Chalabi, Agnes Legrand, Julie Renard, Emmanuel Tejerina, Marina Daouya, Sylvie Fabrega, Jérôme Megret, Robert Olaso, Anne Boland and 4 more

Full text read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

14 authors.

Victoria MichaelsUniversité Paris Cité, CNRS, INSERM, Institut Necker Enfants Malades-INEM, 75015 Paris, France.
Smahane ChalabiUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057 Evry, France.ORCID 0000-0002-2203-3722
Agnes LegrandUniversité Paris Cité, CNRS, INSERM, Institut Necker Enfants Malades-INEM, 75015 Paris, France.ORCID 0000-0002-1063-2816
Julie RenardAtomic Energy and Alternative Energies Agency (CEA), Department of Research in Hemato-Immunology (SRHI), Saint-Louis Hospital, 75010 Paris, France.
Emmanuel TejerinaUniversité Paris Cité, CNRS, INSERM, Institut Necker Enfants Malades-INEM, 75015 Paris, France.ORCID 0000-0001-8673-1493
Marina DaouyaAtomic Energy and Alternative Energies Agency (CEA), Department of Research in Hemato-Immunology (SRHI), Saint-Louis Hospital, 75010 Paris, France.ORCID 0000-0002-4002-9401
Sylvie FabregaSFR Necker-US24/UAR 3633/-Structure Fédérative de Recherche Necker Plateformes Vecteurs Viraux et Transfert de Gènes et Cytométrie, Faculté de Médecine de Necker, 75015 Paris, France.ORCID 0000-0002-4145-5488
Jérôme MegretSFR Necker-US24/UAR 3633/-Structure Fédérative de Recherche Necker Plateformes Vecteurs Viraux et Transfert de Gènes et Cytométrie, Faculté de Médecine de Necker, 75015 Paris, France.
Robert OlasoUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057 Evry, France.
Anne BolandUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057 Evry, France.
Jean-François DeleuzeUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057 Evry, France.
Christophe BattailUniversité Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057 Evry, France.ORCID 0000-0001-6849-7824
Diana Tronik-Le RouxAtomic Energy and Alternative Energies Agency (CEA), Department of Research in Hemato-Immunology (SRHI), Saint-Louis Hospital, 75010 Paris, France.
Sophie EzineUniversité Paris Cité, CNRS, INSERM, Institut Necker Enfants Malades-INEM, 75015 Paris, France.

Funding

Fondation de la Recherche Médicale (FRM) Bioinformatics Analysis for Biology Research program DBI20131228570
6 · The paper itself

Abstract

T cells have the potential to maintain immunological memory and self-tolerance by recognizing antigens from pathogens or tumors. In pathological situations, failure to generate de novo T cells causes immunodeficiency resulting in acute infections and complications. Hematopoietic stem cells (HSC) transplantation constitutes a valuable option to restore proper immune function. However, delayed T cell reconstitution is observed compared to other lineages. To overcome this difficulty, we developed a new approach to identify populations with efficient lymphoid reconstitution properties. To this end, we use a DNA barcoding strategy based on the insertion into a cell chromosome of a lentivirus (LV) carrying a non-coding DNA fragment named barcode (BC). These will segregate through cell divisions and be present in cells' progeny. The remarkable characteristic of the method is that different cell types can be tracked simultaneously in the same mouse. Thus, we in vivo barcoded LMPP and CLP progenitors to test their ability to reconstitute the lymphoid lineage. Barcoded progenitors were co-grafted in immuno-compromised mice and their fate analyzed by evaluating the BC composition in transplanted mice. The results highlight the predominant role of LMPP progenitors for lymphoid generation and reveal valuable novel insights to be reconsidered in clinical transplantation assays.

Indexed as

Hematopoietic Stem Cell TransplantationLymphocytesAnimalsCell DifferentiationCell LineageHematopoietic Stem CellsMiceT-Lymphocytesbone marrow graftcell labelingcytometrydifferentiationgenome barcodinghigh-throughput DNA-sequencinglentiviruslymphoid progenitorsthymus

Identifiers

PMID36901798
PMCPMC10002536

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Textfull text, public
LicenceCC BY
measurements read58
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.