Evidence map›Paper›PMID 41478939›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Humanized Murine Model with Peripheral Blood Mononuclear Cells as a Strategy to Translate Experimental Biomedical Research.

Matheus R Gonçalves, Victor R M Costa, Jennifer R Martins, Viviane L Batista, Jéssica A B Pereira, Fernanda L Tana, Walison Nunes Silva, Pedro P G Guimarães, Barbara Maximino Rezende, Vanessa Pinho and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Matheus R GonçalvesDepartamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0009-0008-0798-9778
Victor R M CostaDepartamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0009-0004-4525-7907
Jennifer R MartinsDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0002-2916-2631
Viviane L BatistaDepartamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0002-7821-9841
Jéssica A B PereiraDepartamento de Fisiologia e Biofísica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0009-0003-3309-5042
Fernanda L TanaDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0002-4692-0836
Walison Nunes SilvaDepartamento de Fisiologia e Biofísica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0003-2654-7795
Pedro P G GuimarãesDepartamento de Fisiologia e Biofísica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0003-4534-2779
Barbara Maximino RezendeDepartamento de Patologia Geral, Programa de Pós-Graduação em Biologia Celular, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0001-7959-7732
Vanessa PinhoDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0003-1038-2324
Mauro Martins TeixeiraDepartamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0002-6944-3008
Jordana G A Coelho-Dos-ReisDepartamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0003-2591-0679
Celso Martins Queiroz-JuniorDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil.ORCID https://orcid.org/0000-0002-7884-7709
Vivian V CostaDepartamento de Morfologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte-MG, Brazil. vivianvcosta@ufmg.br.ORCID https://orcid.org/0000-0002-0175-642X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the main limitations to developing new therapies for human diseases and understanding their pathogenicity mechanisms is difficulty to translate the results obtained in animal models to the clinic. Factors such as the existence of pathogens with unique tropism for human cells and the evolutionary differences between human and animal models often limit the effectiveness of the studies. On the other hand, animal models have been widely used to investigate disease mechanisms due to their shorter lifespans, small size, and easy maintenance. Many advances in the understanding of physiology and genetic architecture enable the development of new models and strategies to overcome species limitations. In this context, humanized mice have emerged as a powerful tool for the investigation of human diseases. Animal models without functional immune system allow the engraftment of human cells and tissues to study human infectious pathogens, tissue transplantation, as well as the human immune system function and ontogeny. Although this model can be limited by the onset of graft-versus-host disease (GVHD), it allows the investigation of this specific disease. Here in this chapter, we describe an experimental platform of peripheral blood mononuclear cell (PBMC) humanized mice and methods related to the model.

Indexed as

Disease Models, AnimalLeukocytes, MononuclearTranslational Research, BiomedicalAnimalsGraft vs Host DiseaseHumansMiceMice, SCIDAnimal modelHuman diseasesHumanized micePBMC

Identifiers

PMID41478939

What OpenQuestion holds

Textmetadata
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.