Evidence map›Paper›PMID 30664659›Full record

ArticleNature communications2019

A highly efficient and faithful MDS patient-derived xenotransplantation model for pre-clinical studies.

Yuanbin Song, Anthony Rongvaux, Ashley Taylor, Tingting Jiang, Toma Tebaldi, Kunthavai Balasubramanian, Arun Bagale, Yunus Kasim Terzi, Rana Gbyli, Xiaman Wang and 13 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
9.0field-weighted citation impact, top 2% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Humanized mouse models in MDS.Cell death & disease · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Discovery of U2AF1 neoantigens in myeloid neoplasms.Journal for immunotherapy of cancer · 2023
    Article
  18. IL-6 trans-signaling in a humanized mouse model of scleroderma.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Article
  20. 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

23 authors at 6 institutions in 5 countries.

Yuanbin SongSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-5580-5998
Anthony RongvauxDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-7142-6533
Ashley TaylorSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
Tingting JiangDepartment of Pathology, Yale University School of Medicine, New Haven, CT, USA.
Toma TebaldiSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-0625-1631
Kunthavai BalasubramanianSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
Arun BagaleSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0003-2304-6610
Yunus Kasim TerziSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-5612-9696
Rana GbyliSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
Xiaman WangSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
Xiaoying FuSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
Yimeng GaoSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0003-2954-2789
Jun ZhaoDepartment of Pathology, Yale University School of Medicine, New Haven, CT, USA.
Nikolai PodoltsevSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-3657-778X
Mina XuDepartment of Pathology, Yale University School of Medicine, New Haven, CT, USA.
Natalia NeparidzeSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
Ellice WongSection of Hematology/Oncology, VA Medical Center, West Haven, CT, USA.
Richard TorresDepartment of Laboratory Medicine, Yale University School of Medicine, New Haven, CT, USA.
Emanuela M BrusciaDepartment of Pediatrics, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0003-2149-4057
Yuval KlugerDepartment of Pathology, Yale University School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-3035-071X
Markus G ManzHematology, University Hospital and University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-4676-7931
Richard A FlavellDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA. richard.flavell@yale.edu.ORCID http://orcid.org/0000-0003-4461-0778
Stephanie HaleneSection of Hematology, Department of Internal Medicine and Yale Comprehensive Cancer Center, Yale University School of Medicine, New Haven, CT, USA. stephanie.halene@yale.edu.ORCID http://orcid.org/0000-0002-2737-9810
Yale Cancer Center · USYale University · USBaşkent University · TRHoward Hughes Medical Institute · USUniversity of Trento · ITUniversity of Zurich · CH

Funding

Yale Cooperative Hematology Specialized Core CenterU54DK106857 · NIDDK · YALE UNIVERSITY · PI JOHN HWA, Diane S Krause · 2015 to 2026
$9.7M
Understanding Hemotopoietic Neoplasias using Humanized MiceR01CA156689 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V, FLAVELL, RICHARD A · 2010 to 2014
$5.0M
CFTR and Toll-Like Receptor SignalingR01HL123851 · NHLBI · YALE UNIVERSITY · PI BRUSCIA, EMANUELA MARINA · 2016 to 2019
$1.7M
The role of mutant splicing factor SRSF2 in MyelodysplasiaR01DK102792 · NIDDK · YALE UNIVERSITY · PI HALENE, STEPHANIE · 2016 to 2019
$1.5M
EFFICIENT SPECTRAL APPROACHES FOR FINDING UNDERLYING STRUCTURES IN BIG DATAR01HG008383 · NHGRI · YALE UNIVERSITY · PI KLUGER, YUVAL · 2016 to 2018
$1.2M
Assessing nuclear morphology in thick tissues using fLCIR21CA120128 · NCI · DUKE UNIVERSITY · PI WAX, ADAM · 2006 to 2007
$255k
NCI NIH HHS R01 CA156689NCI NIH HHS R21 CA120128NHGRI NIH HHS R01 HG008383NHLBI NIH HHS R01 HL123851NIDDK NIH HHS R01 DK102792NIDDK NIH HHS U54 DK106857
6 · The paper itself

Abstract

Comprehensive preclinical studies of Myelodysplastic Syndromes (MDS) have been elusive due to limited ability of MDS stem cells to engraft current immunodeficient murine hosts. Here we report a MDS patient-derived xenotransplantation model in cytokine-humanized immunodeficient "MISTRG" mice that provides efficient and faithful disease representation across all MDS subtypes. MISTRG MDS patient-derived xenografts (PDX) reproduce patients' dysplastic morphology with multi-lineage representation, including erythro- and megakaryopoiesis. MISTRG MDS-PDX replicate the original sample's genetic complexity and can be propagated via serial transplantation. MISTRG MDS-PDX demonstrate the cytotoxic and differentiation potential of targeted therapeutics providing superior readouts of drug mechanism of action and therapeutic efficacy. Physiologic humanization of the hematopoietic stem cell niche proves critical to MDS stem cell propagation and function in vivo. The MISTRG MDS-PDX model opens novel avenues of research and long-awaited opportunities in MDS research.

Indexed as

Disease Models, AnimalGraft SurvivalAnimalsAntigens, CDBiomarkersCytokinesGene ExpressionGene Knock-In TechniquesHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansMiceMice, TransgenicMyelodysplastic SyndromesStem Cell NicheTransplantation, HeterologousAntigens, CDBiomarkersCytokines

Identifiers

PMID30664659
PMCPMC6341122
OpenAlexW2949496869

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.