Evidence map›Paper›PMID 33854497›Full record

ArticleFrontiers in immunology2021

Testing Cancer Immunotherapy in a Human Immune System Mouse Model: Correlating Treatment Responses to Human Chimerism, Therapeutic Variables and Immune Cell Phenotypes.

Juan A Marín-Jiménez, Anna Capasso, Matthew S Lewis, Stacey M Bagby, Sarah J Hartman, Jeremy Shulman, Natalie M Navarro, Hui Yu, Chris J Rivard, Xiaoguang Wang and 21 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Trial
  2. Humanized immune system animal models and their recent applications.Animal models and experimental medicine · 2026
    Review
  3. Article
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  9. Article
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  13. Fetal liver CD34Stem cell research & therapy · 2024
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Humanized mouse models for immuno-oncology research.Nature reviews. Clinical oncology · 2023
    Review
  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

31 authors at 6 institutions in 2 countries.

Juan A Marín-JiménezDepartment of Medical Oncology, Catalan Institute of Oncology (ICO-L'Hospitalet), Barcelona, Spain.
Anna CapassoDepartment of Oncology, Livestrong Cancer Institutes, Dell Medical School, University of Texas at Austin, Austin, TX, United States.
Matthew S LewisDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
Stacey M BagbyDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Sarah J HartmanDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Jeremy ShulmanDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
Natalie M NavarroDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Hui YuDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Chris J RivardDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Xiaoguang WangDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
Jessica C BarkowDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
Degui GengDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Adwitiya KarDivision of Endocrinology, School of Medicine, University of Colorado, Aurora, CO, United States.
Ashley YingstDepartment of Pediatrics, School of Medicine, University of Colorado, Aurora, CO, United States.
Dejene M TufaDepartment of Pediatrics, School of Medicine, University of Colorado, Aurora, CO, United States.
James T DolanRocky Vista College of Osteopathic Medicine - OMS3, Rocky Vista University, Parker, CO, United States.
Patrick J BlatchfordDepartment of Biostatistics and Informatics, Colorado School of Public Health, University of Colorado Denver, Aurora, CO, United States.
Brian M FreedDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
Raul M TorresDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
Eduardo DavilaDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Jill E SlanskyDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
Roberta PelandaDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
S Gail EckhardtDepartment of Oncology, Livestrong Cancer Institutes, Dell Medical School, University of Texas at Austin, Austin, TX, United States.
Wells A MessersmithDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Jennifer R DiamondDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Christopher H LieuDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Michael R VernerisDepartment of Pediatrics, School of Medicine, University of Colorado, Aurora, CO, United States.
Jing H WangDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
Katja Kiseljak-VassiliadesUniversity of Colorado Cancer Center, Aurora, CO, United States.
Todd M PittsDivision of Medical Oncology, School of Medicine, University of Colorado, Aurora, CO, United States.
Julie LangDepartment of Immunology and Microbiology, School of Medicine, University of Colorado, Aurora, CO, United States.
University of Colorado Anschutz Medical Campus · USUniversity of Colorado Cancer Center · USLivestrong Foundation · USColorado School of Public Health · USInstitut Català d'Oncologia · ESRocky Vista University · US

Funding

Lysophosphatidic Acid Regulation of CD8 T cell activation and functionR01AI143261 · NIAID · UNIVERSITY OF COLORADO DENVER · PI TORRES, RAUL MARTIN · 2020 to 2024
$2.6M
Developing newly combined therapeutic strategies for mature B cell lymphomaR01CA229174 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JING HONG · 2019 to 2023
$2.5M
Studies of human B cell tolerance, from a humanized mouse model to human beingsR01AI124474 · NIAID · UNIVERSITY OF COLORADO DENVER · PI PELANDA, ROBERTA · 2016 to 2020
$2.3M
Utilizing MEK Inhibition to Sensitize Microsatellite Stable Colorectal Cancer to Immune Checkpoint TherapyR01CA229259 · NCI · UNIVERSITY OF COLORADO DENVER · PI LIEU, CHRISTOPHER HANYOUNG · 2018 to 2020
$1.3M
Noninvasive detection of circulating RNAs for lung cancer early detection and prognosisR33CA191245 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI WU, YUN · 2015 to 2018
$1.3M
Identifying and Characterizing Therapeutic Targets in Adrenal CancerK08CA222620 · NCI · UNIVERSITY OF COLORADO DENVER · PI KISELJAKVASSILIADES, KATJA · 2018 to 2022
$1.0M
BLRD VA I01 BX004665NCI NIH HHS K08 CA222620NCI NIH HHS R01 CA229174NCI NIH HHS R01 CA229259NCI NIH HHS R33 CA191245NIAID NIH HHS R01 AI124474NIAID NIH HHS R01 AI143261
6 · The paper itself

Abstract

Over the past decade, immunotherapies have revolutionized the treatment of cancer. Although the success of immunotherapy is remarkable, it is still limited to a subset of patients. More than 1500 clinical trials are currently ongoing with a goal of improving the efficacy of immunotherapy through co-administration of other agents. Preclinical, small-animal models are strongly desired to increase the pace of scientific discovery, while reducing the cost of combination drug testing in humans. Human immune system (HIS) mice are highly immune-deficient mouse recipients rtpeconstituted with human hematopoietic stem cells. These HIS-mice are capable of growing human tumor cell lines and patient-derived tumor xenografts. This model allows rapid testing of multiple, immune-related therapeutics for tumors originating from unique clinical samples. Using a cord blood-derived HIS-BALB/c-Rag2

Indexed as

Disease Models, AnimalHeterograftsImmune SystemImmunotherapyAnimalsChimerismHematopoietic Stem Cell TransplantationHumansLymphocyte SubsetsLymphoid TissueMiceMice, Inbred NODMice, KnockoutMice, SCIDNeoplasmsPhenotypecheckpoint blockadecombination testinghumanized miceimmune correlatesimmunotherapyPDX (patient derived xenograft)preclinical modelTME (tumor microenvironment)

Identifiers

PMID33854497
PMCPMC8040953
OpenAlexW3143803822

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.