Evidence map›Paper›PMID 33058566›Full record

ReviewStem cells translational medicine2021

Advances in preclinical hematopoietic stem cell models and possible implications for improving therapeutic transplantation.

Ellen Fraint, Bianca A Ulloa, María Feliz Norberto, Kathryn S Potts, Teresa V Bowman

Abstract readReview
In one paragraph

Review in Stem cells translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Phenylethanoid Glycosides fromInternational journal of molecular sciences · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. An Overview of Autophagy in Hematopoietic Stem Cell Transplantation.Frontiers in bioengineering and biotechnology · 2022
    Review
  11. Article
  12. Basic and Preclinical Research for Personalized Medicine.Journal of personalized medicine · 2021
    Review
  13. 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

5 authors.

Ellen FraintDepartment of Pediatrics, Children's Hospital at Montefiore, Bronx, New York, USA.ORCID 0000-0001-5548-0206
Bianca A UlloaDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York, USA.ORCID 0000-0003-2020-0141
María Feliz NorbertoDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York, USA.ORCID 0000-0003-2447-6647
Kathryn S PottsDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York, USA.ORCID 0000-0002-3246-9597
Teresa V BowmanDepartment of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York, USA.ORCID 0000-0002-6103-6862

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007288 · NIGMS · YESHIVA UNIVERSITY · PI AKABAS, MYLES H. · 1985 to 2022
$35.6M
Einstein Postbaccalaureate Research Education ProgramR25GM104547 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI AKABAS, MYLES H. · 2013 to 2023
$4.0M
Deciphering the development of hematopoietic stem and progenitor cell self-renewal and differentiationF31HL152562 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI ULLOA, BIANCA A · 2020 to 2023
$206k
Crosstalk of Splicing and Signaling during HSC FormationR56DK121738 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BOWMAN, TERESA V · 2019 to 2019
$100k
NHLBI NIH HHS F31 HL152562NIDDK NIH HHS R56 DK121738NIGMS NIH HHS R25 GM104547NIGMS NIH HHS T32 GM007288
6 · The paper itself

Abstract

Hematopoietic stem cell transplantation (HSCT) is a treatment for many malignant, congenital, and acquired hematologic diseases. Some outstanding challenges in the HSCT field include the paucity of immunologically-matched donors, our inability to effectively expand hematopoeitic stem cells (HSCs) ex vivo, and the high infection risk during engraftment. Scientists are striving to develop protocols to generate, expand, and maintain HSCs ex vivo, however these are not yet ready for clinical application. Given these problems, advancing our understanding of HSC specification, regulation, and differentiation in preclinical models is essential to improve the therapeutic utility of HSCT. In this review, we link biomedical researchers and transplantation clinicians by discussing the potential therapeutic implications of recent fundamental HSC research in model organisms. We consider deficiencies in current HSCT practice, such as problems achieving adequate cell dose for successful and rapid engraftment, immense inflammatory cascade activation after myeloablation, and graft-vs-host disease. Furthermore, we discuss recent advances in the field of HSC biology and transplantation made in preclinical models of zebrafish, mouse, and nonhuman primates that could inform emerging practice for clinical application.

Indexed as

Disease Models, AnimalHematopoietic Stem Cell TransplantationAnimalsGraft vs Host DiseaseHematopoietic Stem CellsMicePrimatesTransplantation ConditioningZebrafishgraft-vs-host diseasehematopoietic stem cellslineage tracingpreclinical modelstransplantation

Identifiers

PMID33058566
PMCPMC7900582

What Socratic 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 Socratic graph.