Evidence map›Paper›PMID 32582159›Full record

ArticleFrontiers in immunology2020

Macrophages Derived From Human Induced Pluripotent Stem Cells Are Low-Activated "Naïve-Like" Cells Capable of Restricting Mycobacteria Growth.

Tatiana Nenasheva, Tatiana Gerasimova, Yana Serdyuk, Elena Grigor'eva, George Kosmiadi, Alexander Nikolaev, Erdem Dashinimaev, Irina Lyadova

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 41 citations in OpenAlex.

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  7. High-throughput screening of small molecules targetingAntimicrobial agents and chemotherapy · 2025
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  15. A Model of iPSC-Derived Macrophages withInternational journal of molecular sciences · 2023
    Article
  16. Functional genomics in stem cell models: considerations and applications.Frontiers in cell and developmental biology · 2023
    Review
  17. 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

8 authors at 3 institutions in 1 country.

Tatiana NenashevaLaboratory of Cellular and Molecular Basis of Histogenesis, Koltzov Institute of Developmental Biology of the Russian Academy of Sciences, Moscow, Russia.
Tatiana GerasimovaLaboratory of Cellular and Molecular Basis of Histogenesis, Koltzov Institute of Developmental Biology of the Russian Academy of Sciences, Moscow, Russia.
Yana SerdyukLaboratory of Cellular and Molecular Basis of Histogenesis, Koltzov Institute of Developmental Biology of the Russian Academy of Sciences, Moscow, Russia.
Elena Grigor'evaLaboratory of Developmental Epigenetics, Federal Research Center Institute of Cytology and Genetics, The Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.
George KosmiadiLaboratory of Biotechnology, Department of Immunology, Central Tuberculosis Research Institute, Moscow, Russia.
Alexander NikolaevLaboratory of Biotechnology, Department of Immunology, Central Tuberculosis Research Institute, Moscow, Russia.
Erdem DashinimaevCenter for Genome Technologies, Pirogov Russian National Research Medical University, Moscow, Russia.
Irina LyadovaLaboratory of Cellular and Molecular Basis of Histogenesis, Koltzov Institute of Developmental Biology of the Russian Academy of Sciences, Moscow, Russia.
Koltzov Institute of Developmental Biology · RUCentral Scientific Research Institute of Tuberculosis Russian Academy of Medical Sciences · RUInstitute of Cytology and Genetics · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In peripheral tissues, immune protection critically depends on the activity of tissue resident macrophages, which makes our understanding of the biology of these cells of great significance. Until recently, human macrophage studies were largely based on the analysis of monocyte-derived macrophages that differ from tissue resident macrophages by many characteristics. To model tissue resident macrophages, methods of generating macrophages from pluripotent stem cells have been developed. However, the immunological properties of macrophages derived from pluripotent stem cells remain under-investigated. In this study, we aimed to perform the multifarious immunological characteristics of macrophages generated from human induced pluripotent stem cells (iMϕs), including an analysis of their phenotype, secretory and antibacterial activities, as well as their comparison with macrophages derived from blood monocytes and infected lung tissue. We report that iMϕs displayed the morphology and the CD11b

Indexed as

Antigens, CDCell Culture TechniquesCell DifferentiationCells, CulturedCytokinesHumansImmunophenotypingInduced Pluripotent Stem CellsInflammationLungMacrophage ActivationMacrophagesMycobacterium tuberculosisPhagocytosisTuberculosisAntigens, CDCytokinesCD16chemokinescytokinesHLA-DRinduced pluripotent stem cell derived macrophagesM1 and M2 macrophagesMycobacterium tuberculosis

Identifiers

PMID32582159
PMCPMC7287118
OpenAlexW3033031190

What OpenQuestion holds

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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.