Evidence map›Paper›PMID 29630967›Full record

ArticleJournal of immunological methods2018

Inducible disruption of the c-myb gene allows allogeneic bone marrow transplantation without irradiation.

C Stremmel, R Schuchert, V Schneider, T Weinberger, R Thaler, D Messerer, S Helmer, F Geissmann, J Frampton, S Massberg and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of immunological methods, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Two populations of self-maintaining monocyte-independent macrophages exist in adult epididymis and testis.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  4. Article
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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

11 authors at 5 institutions in 3 countries.

C StremmelMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany.
R SchuchertMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany.
V SchneiderMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany.
T WeinbergerMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany.
R ThalerMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany.
D MessererMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany.
S HelmerMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany.
F GeissmannImmunology Program, Memorial Sloan Kettering Cancer Center (MSKCC), New York, NY 10065, USA.
J FramptonInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
S MassbergMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; DZHK (German Center for Cardiovascular Research), Partner Site Munich Heart Alliance, Biedersteiner Strasse 29, Munich 80802, Germany.
C SchulzMedizinische Klinik und Poliklinik I, Klinikum der Universität, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; Walter-Brendel-Center for Experimental Medicine, Ludwig Maximilians-Universität, Marchioninistrasse 15, Munich 81377, Germany; DZHK (German Center for Cardiovascular Research), Partner Site Munich Heart Alliance, Biedersteiner Strasse 29, Munich 80802, Germany. Electronic address: christian.schulz@med.uni-muenchen.de.
Ludwig-Maximilians-Universität München · DELMU Klinikum · DEGerman Centre for Cardiovascular Research · DEMemorial Sloan Kettering Cancer Center · USUniversity of Birmingham · GB

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Macrophage development and specification in mice.R01AI130345 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI Frederic Geissmann · 2017 to 2026
$5.7M
Lineages and pathophysiology of clonal histiocytic disordersR01HL138090 · NHLBI · SLOAN-KETTERING INST CAN RESEARCH · PI GEISSMANN, FREDERIC · 2017 to 2020
$2.9M
NCI NIH HHS P30 CA008748NHLBI NIH HHS R01 HL138090NIAID NIH HHS R01 AI130345
6 · The paper itself

Abstract

Allogeneic bone marrow (BM) transplantation enables the in vivo functional assessment of hematopoietic cells. As pre-conditioning, ionizing radiation is commonly applied to induce BM depletion, however, it exerts adverse effects on the animal and can limit experimental outcome. Here, we provide an alternative method that harnesses conditional gene deletion to ablate c-myb and thereby deplete BM cells, hence allowing BM substitution without other pre-conditioning. The protocol results in a high level of blood chimerism after allogeneic BM transplantation, whereas immune cells in peripheral tissues such as resident macrophages are not replaced. Further, mice featuring a low chimerism after initial transplantation can undergo a second induction cycle for efficient deletion of residual BM cells without the necessity to re-apply donor cells. In summary, we present an effective c-myb-dependent genetic technique to generate BM chimeras in the absence of irradiation or other methods for pre-conditioning.

Indexed as

Gene DeletionTransplantation ChimeraAnimalsBone Marrow TransplantationFemaleGenes, mybHematopoietic Stem Cell TransplantationImmune ToleranceMaleMiceMice, Inbred C57BLPoly I-CRadiation, IonizingTransplantation ConditioningTransplantation, HomologousPoly I-CBone marrowChimeraC-mybConditional deletionHematopoietic stem cellsTransplantation

Identifiers

PMID29630967
PMCPMC6022737
OpenAlexW2795559730

What OpenQuestion holds

Textmetadata
LicenceTDM
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.