Evidence map›Paper›PMID 34057741›Full record

ArticleJournal of leukocyte biology2022

A novel clinically relevant graft-versus-leukemia model in humanized mice.

Bei Jia, Chenchen Zhao, Michael Bayerl, Hiroko Shike, David F Claxton, W Christopher Ehmann, Shin Mineishi, Todd D Schell, Pan Zheng, Yi Zhang and 4 more

Open access · greenAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2022. 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
0.7field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. 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 at 5 institutions in 1 country.

Bei JiaPenn State Cancer Institute, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Chenchen ZhaoPenn State Cancer Institute, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Michael BayerlDepartment of Pathology, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Hiroko ShikeDepartment of Pathology, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
David F ClaxtonPenn State Cancer Institute, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
W Christopher EhmannPenn State Cancer Institute, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Shin MineishiPenn State Cancer Institute, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Todd D SchellPenn State Cancer Institute, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Pan ZhengDepartment of Surgery, Division of Immunotherapy, Institute of Human Virology, University of Maryland Baltimore School of Medicine, Baltimore, Maryland, USA.
Yi ZhangDepartment of Microbiology and Immunology, Fels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, Pennsylvania, USA.
Leonard D ShultzDepartment of Immunology, The Jackson Laboratory, Bar Harbor, Maine, USA.
K Sandeep PrabhuDepartment of Veterinary and Biomedical Sciences, Penn State University, University Park, Pennsylvania, USA.
Robert F PaulsonDepartment of Veterinary and Biomedical Sciences, Penn State University, University Park, Pennsylvania, USA.
Hong ZhengPenn State Cancer Institute, Penn State University College of Medicine, Hershey, Pennsylvania, USA.
Pennsylvania State University · USPenn State Milton S. Hershey Medical Center · USJackson Laboratory · USTemple University · USUniversity of Maryland, Baltimore · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Pathology CoreP50CA254897 · NCI · CORIELL INSTITUTE FOR MEDICAL RESEARCH · PI ISSA, JEAN-PIERRE J. · 2021 to 2025
$11.9M
NCI NIH HHS P30 CA034196NCI NIH HHS P50 CA254897
6 · The paper itself

Abstract

The prognosis for acute myeloid leukemia (AML) relapse post allogeneic hematopoietic stem cell transplantation (alloSCT) is dismal. Novel effective treatment is urgently needed. Clinical benefit of alloSCT greatly relies on the graft-versus-leukemia (GVL) effect. The mechanisms that mediate immune escape of leukemia (thus causing GVL failure) remain poorly understood. Studies of human GVL have been hindered by the lack of optimal clinically relevant models. Here, using our large, longitudinal clinical tissue bank that include AML cells and G-CSF mobilized donor hematopoietic stem cells (HSCs), we successfully established a novel GVL model in humanized mice. Donor HSCs were injected into immune-deficient NOD-Cg-Prkdc

Indexed as

Disease Models, AnimalAnimalsGraft vs Leukemia EffectGranulocyte Colony-Stimulating FactorHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMiceMice, Inbred NODMice, SCIDTransplantation, HomologousGranulocyte Colony-Stimulating FactorAMLGVLNSGT cells

Identifiers

PMID34057741
PMCPMC8922387
OpenAlexW3165835525

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.