Evidence map›Paper›PMID 24248605›Full record

ReviewImmunologic research2013

Humanized mice: novel model for studying mechanisms of human immune-based therapies.

Louis Gonzalez, Natasa Strbo, Eckhard R Podack

Open access · greenAbstract readReview
In one paragraph

Review in Immunologic research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

23 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Rat and Mouse Brain Tumor Models for Experimental Neuro-Oncology Research.Journal of neuropathology and experimental neurology · 2022
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Animal models of tuberculosis: Lesson learnt.The Indian journal of medical research · 2018
    Review
  15. Antiretroviral Drug Metabolism in Humanized PXR-CAR-CYP3A-NOG Mice.The Journal of pharmacology and experimental therapeutics · 2018
    Article
  16. Article
  17. CD38 as a PET Imaging Target in Lung Cancer.Molecular pharmaceutics · 2017
    Article
  18. Article
  19. Review
  20. Article
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

3 authors at 1 institution in 1 country.

Louis GonzalezDepartment of Microbiology and Immunology, Miller School of Medicine, University of Miami, Miami, FL, USA.
Natasa Strbo
Eckhard R Podack
University of Miami · US

Funding

Miami Clinical and Translational Science InstituteUL1TR000460 · NCATS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SACCO, RALPH L. · 2012 to 2016
$16.9M
REGULATION OF ANTI-TUMOR IMMUNITYP01CA109094 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI CRAY, CAROLYN · 2007 to 2011
$6.2M
BIOPSYCHOSOCIAL RESEARCH TRAINING IN IMMUNOLOGY AND AIDST32MH018917 · NIMH · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SCHNEIDERMAN, NEIL · 1989 to 2013
$3.5M
Miami Clinical and Translational Science InstituteKL2TR000461 · NCATS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI SACCO, RALPH L. · 2012 to 2016
$2.1M
Response to and protection by gp96SIVIg/TNFSF13 and gp96SIVIg/TNFSF15 vaccinesP01AI096396 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PODACK, ECKHARD R · 2011 to 2011
$2.0M
Induction of mucosal SIV immunity in non human primates by secreted Hsp-Gp96R33AI073234 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PODACK, ECKHARD R · 2009 to 2011
$1.7M
Induction of mucosal SIV immunity in non human primates by secreted Hsp-Gp96R21AI073234 · NIAID · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI PODACK, ECKHARD R · 2007 to 2008
$415k
NCATS NIH HHS 1KL2TR000461NCATS NIH HHS KL2 TR000461NCATS NIH HHS NCATS NIH UL1TR000460NCATS NIH HHS UL1 TR000460NCI NIH HHS P01 CA109094NIAID NIH HHS P01 AI096396NIAID NIH HHS R21 AI073234NIAID NIH HHS R33 AI073234NIMH NIH HHS AIDS 5T32MH018917-22NIMH NIH HHS T32 MH018917PHS HHS NIAID R33 AI073234PHS HHS NIH P30A1073961
6 · The paper itself

Abstract

The lack of relevant animal models is the major bottleneck for understanding human immunology and immunopathology. In the last few years, a novel model of humanized mouse has been successfully employed to investigate some of the most critical questions in human immunology. We have set up and tested in our laboratory the latest technology for generating mice with a human immune system by reconstituting newborn immunodeficient NOD/SCID-γ(c)(-/-) mice with human fetal liver-derived hematopoietic stem cells. These humanized mice have been deemed most competent as human models in a thorough comparative study with other humanized mouse technologies. Lymphocytes in these mice are of human origin while other hematopoietic cells are chimeric, partly of mouse and partly of human origin. We demonstrate that human CD8 T lymphocytes in humanized mice are fully responsive to our novel cell-based secreted heat shock protein gp96(HIV)-Ig vaccine. We also show that the gp96(HIV)-Ig vaccine induces powerful mucosal immune responses in the rectum and the vagina, which are thought to be required for protection from HIV infection. We posit the hypothesis that vaccine approaches tested in humanized mouse models can generate data rapidly, economically and with great flexibility (genetic manipulations are possible), to be subsequently tested in larger nonhuman primate models and humans.

Indexed as

Immune SystemImmunotherapyMiceModels, AnimalAnimalsDisease Models, AnimalHematopoietic Stem Cell TransplantationHumansMice, Inbred NODMice, SCID

Identifiers

PMID24248605
PMCPMC3966553
OpenAlexW1985264178

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.