Evidence map›Paper›PMID 35959876›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2022

Enhanced development of functional human NK cells in NOD-scid-IL2rg

Ken-Edwin Aryee, Lisa M Burzenski, Li-Chin Yao, James G Keck, Dale L Greiner, Leonard D Shultz, Michael A Brehm

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  7. Humanized immune system animal models and their recent applications.Animal models and experimental medicine · 2026
    Review
  8. Article
  9. Article
  10. Humanized mice enableMolecular therapy. Advances · 2026
    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

7 authors at 2 institutions in 1 country.

Ken-Edwin AryeeProgram in Molecular Medicine, Diabetes Center of Excellence, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Lisa M BurzenskiThe Jackson Laboratory, Bar Harbor, Massachusetts, USA.
Li-Chin YaoThe Jackson Laboratory, Sacramento, California, USA.
James G KeckThe Jackson Laboratory, Sacramento, California, USA.
Dale L GreinerProgram in Molecular Medicine, Diabetes Center of Excellence, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Leonard D ShultzThe Jackson Laboratory, Bar Harbor, Massachusetts, USA.
Michael A BrehmProgram in Molecular Medicine, Diabetes Center of Excellence, University of Massachusetts Chan Medical School, Worcester, Massachusetts, USA.
Jackson Laboratory · USUniversity of Massachusetts Chan Medical School · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Humanized Mouse Avatars for T1DU01DK104218 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, GREINER, DALE LESLIE · 2019 to 2023
$4.5M
Novel humanized mouse model developed from cord blood CD34 positive HSC and autologous iPS cell derived thymusR01AI132963 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, MAEHR, RENE · 2017 to 2021
$4.4M
Live imaging of SARS-CoV-2 infection in novel humanized miceR24OD026440 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, EMERSON, CHARLES P. · 2019 to 2022
$4.2M
Humanized Mouse Avatars for T1DUC4DK104218 · NIDDK · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, DALEY, GEORGE Q · 2014 to 2014
$4.1M
Development and Validation of Novel NSG Mouse Models for Human Stem Cell TherapyR24OD018259 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BREHM, MICHAEL ALLEN, GREINER, DALE LESLIE · 2014 to 2017
$3.0M
NCI NIH HHS P30 CA034196NIAID NIH HHS R01 AI132963NIDDK NIH HHS U01 DK104218NIDDK NIH HHS UC4 DK104218NIH HHS R24 OD018259NIH HHS R24 OD026440
6 · The paper itself

Abstract

Human innate immunity plays a critical role in tumor surveillance and in immunoregulation within the tumor microenvironment. Natural killer (NK) cells are innate lymphoid cells that have opposing roles in the tumor microenvironment, including NK cell subsets that mediate tumor cell cytotoxicity and subsets with regulatory function that contribute to the tumor immune suppressive environment. The balance between effector and regulatory NK cell subsets has been studied extensively in murine models of cancer, but there is a paucity of models to study human NK cell function in tumorigenesis. Humanized mice are a powerful alternative to syngeneic mouse tumor models for the study of human immuno-oncology and have proven effective tools to test immunotherapies targeting T cells. However, human NK cell development and survival in humanized NOD-scid-IL2rg

Indexed as

Immunity, InnateInterleukin-15AnimalsDisease Models, AnimalHumansInterleukin Receptor Common gamma SubunitKiller Cells, NaturalMiceMice, Inbred NODMice, KnockoutMice, SCIDIL2RG protein, humanIl2rg protein, mouseInterleukin-15Interleukin Receptor Common gamma SubunitHu-IL15humanized miceNK cellsNSGtransgenic

Identifiers

PMID35959876
PMCPMC9383543
OpenAlexW4293374782

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.