Evidence map›Paper›PMID 36591990›Full record

ArticleJournal of visualized experiments : JoVE2022

Testing Cancer Immunotherapeutics in a Humanized Mouse Model Bearing Human Tumors.

Jordi M Lanis, Matthew S Lewis, Hannah Strassburger, Kristina Larsen, Stacey M Bagby, Adrian T A Dominguez, Juan A Marín-Jiménez, Roberta Pelanda, Todd M Pitts, Julie Lang

Erratum issuedOpen access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Jordi M Lanis *Department of Immunology and Microbiology, School of Medicine, University of Colorado Denver Anschutz Medical Campus.
Matthew S Lewis *Department of Immunology and Microbiology, School of Medicine, University of Colorado Denver Anschutz Medical Campus.
Hannah StrassburgerDepartment of Immunology and Microbiology, School of Medicine, University of Colorado Denver Anschutz Medical Campus.
Kristina LarsenDepartment of Immunology and Microbiology, School of Medicine, University of Colorado Denver Anschutz Medical Campus.
Stacey M BagbyDivision of Oncology, School of Medicine, University of Colorado Denver Anschutz Medical Campus.
Adrian T A DominguezDivision of Oncology, School of Medicine, University of Colorado Denver Anschutz Medical Campus.
Juan A Marín-JiménezDepartment of Medical Oncology, Catalan Institute of Oncology (ICO-L'Hospitalet).
Roberta PelandaDepartment of Immunology and Microbiology, School of Medicine, University of Colorado Denver Anschutz Medical Campus.
Todd M PittsDivision of Oncology, School of Medicine, University of Colorado Denver Anschutz Medical Campus.
Julie LangDepartment of Immunology and Microbiology, School of Medicine, University of Colorado Denver Anschutz Medical Campus; Julie.Lang@cuanschutz.edu.
University of Colorado Anschutz Medical Campus · USInstitut Català d'Oncologia · ESUniversity of Colorado Denver · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
CHARACTERIZING AND IMPROVING HUMANIZED IMMUNE SYSTEM MOUSE MODELS (IMM-HIS)75N93020C00058 · NIAID · UNIVERSITY OF COLORADO DENVER · PI LANG, JULIE · 2020 to 2020
$2.0M
NCI NIH HHS P30 CA046934NIAID NIH HHS 75N93020C00058
6 · The paper itself

Abstract

Reversing the immunosuppressive nature of the tumor microenvironment is critical for the successful treatment of cancers with immunotherapy drugs. Murine cancer models are extremely limited in their diversity and suffer from poor translation to the clinic. To serve as a more physiological preclinical model for immunotherapy studies, this protocol has been developed to evaluate the treatment of human tumors in a mouse reconstituted with a human immune system. This unique protocol demonstrates the development of human immune system (HIS, "humanized") mice, followed by implantation of a human tumor, either a cell-line derived xenograft (CDX) or a patient derived xenograft (PDX). HIS mice are generated by injecting CD34+ human hematopoietic stem cells isolated from umbilical cord blood into neonatal BRGS (BALB/c Rag2

Indexed as

NeoplasmsAnimalsDisease Models, AnimalHumansImmunotherapyMiceMice, Inbred NODTransplantation, HeterologousTumor MicroenvironmentXenograft Model Antitumor Assays

Identifiers

PMID36591990
PMCPMC11167650
OpenAlexW4311690570

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.