Evidence map›Paper›PMID 31680058›Full record

ArticleStem cell reports2019

Drug Discovery Platform Targeting M. tuberculosis with Human Embryonic Stem Cell-Derived Macrophages.

Hyo-Won Han, Hyang-Hee Seo, Hye-Yeong Jo, Hyeong-Jun Han, Virgínia C A Falcão, Vincent Delorme, Jinyeong Heo, David Shum, Jang-Hoon Choi, Jin-Moo Lee and 6 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell reports, 2019. 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
2.3field-weighted citation impact, top 11% 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, 47 citations in OpenAlex.

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  11. Nanoscaled Discovery of a Shunt Rifamycin fromACS infectious diseases · 2023
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  16. Review
  17. Human Pluripotent Stem Cell-Derived Alveolar Organoid with Macrophages.International journal of molecular sciences · 2022
    Article
  18. Review
  19. Article
  20. 10-DEBC Hydrochloride as a Promising New Agent against Infection ofInternational journal of molecular sciences · 2022
    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

16 authors at 6 institutions in 2 countries.

Hyo-Won HanDivision of Intractable Diseases, Center for Biomedical Sciences, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea; National Stem Cell Bank of Korea, Korea Institute of Health, Cheongju 28160, Republic of Korea.
Hyang-Hee SeoDivision of Intractable Diseases, Center for Biomedical Sciences, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea; National Stem Cell Bank of Korea, Korea Institute of Health, Cheongju 28160, Republic of Korea.
Hye-Yeong JoDivision of Intractable Diseases, Center for Biomedical Sciences, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea; National Stem Cell Bank of Korea, Korea Institute of Health, Cheongju 28160, Republic of Korea.
Hyeong-Jun HanDivision of Intractable Diseases, Center for Biomedical Sciences, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea.
Virgínia C A FalcãoTuberculosis Research Laboratory, Discovery Biology, Institute Pasteur Korea, Seongnam 13488, Republic of Korea.
Vincent DelormeTuberculosis Research Laboratory, Discovery Biology, Institute Pasteur Korea, Seongnam 13488, Republic of Korea.
Jinyeong HeoScreening Discovery Platform, Screening Sciences and Novel Assay Technologies, Institute Pasteur Korea, Seongnam 13488, Republic of Korea.
David ShumScreening Discovery Platform, Screening Sciences and Novel Assay Technologies, Institute Pasteur Korea, Seongnam 13488, Republic of Korea.
Jang-Hoon ChoiDivision of Viral Disease Research, Center for Infectious Diseases Research, National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea.
Jin-Moo LeeDivision of Viral Disease Research, Center for Infectious Diseases Research, National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea.
Seung Hun LeeDivision of Bacterial Disease Research, Center for Infectious Disease Research, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea.
Hye-Ryeon HeoDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Republic of Korea.
Seok-Ho HongDepartment of Internal Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Republic of Korea.
Mi-Hyun ParkDivision of Intractable Diseases, Center for Biomedical Sciences, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea; National Stem Cell Bank of Korea, Korea Institute of Health, Cheongju 28160, Republic of Korea.
Rajesh K ThimmulappaDepartment of Biochemistry, Center of Excellence in Molecular Biology and Regenerative Medicine, JSS Medical College, JSS Academy of Higher Education & Research, Mysuru 570015, India.
Jung-Hyun KimDivision of Intractable Diseases, Center for Biomedical Sciences, Korea National Institute of Health, Korea Centers for Disease Control and Prevention, Cheongju 28159, Republic of Korea; National Stem Cell Bank of Korea, Korea Institute of Health, Cheongju 28160, Republic of Korea. Electronic address: kjhcorea@korea.kr.
Korea Center for Disease Control and Prevention · KRInstitut Pasteur Korea · KRKorea Disease Control and Prevention Agency · KRKangwon National University · KRJSS Academy of Higher Education and Research · INKorea National Institute of Health · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major limitation in anti-tuberculosis drug screening is the lack of reliable and scalable models for homogeneous human primary macrophage cells of non-cancer origin. Here we report a modified protocol for generating homogeneous populations of macrophage-like cells from human embryonic stem cells. The induced macrophages, referred to as iMACs, presented similar transcriptomic profiles and characteristic immunological features of classical macrophages and were permissive to viral and bacterial infection, in particular Mycobacterium tuberculosis (Mtb). More importantly, iMAC production was amenable to scale up. To evaluate iMAC efficiency in high-throughput anti-tuberculosis drug screening, we performed a phenotypic screening against intracellular Mtb, involving a library of 3,716 compounds that included FDA-approved drugs and other bioactive compounds. Our primary screen identified 120 hits, which were validated in a secondary screen by dose-intracellular and -extracellular Mtb assays. Our confirmatory studies identified a novel anti-Mtb compound, 10-DEBC, also showing activity against drug-resistant strains.

Indexed as

Antitubercular AgentsCell Culture TechniquesCell DifferentiationCell LineCells, CulturedDrug DiscoveryDrug Evaluation, PreclinicalGene Expression ProfilingHuman Embryonic Stem CellsHumansMacrophagesMycobacterium tuberculosisPhagocytosisSmall Molecule LibrariesAntitubercular AgentsSmall Molecule Librariesanti-tuberculosis compounddrug discovery platformhuman embryonic stem cell-derived induced macrophage-like cells (iMACs)Mycobacterium tuberculosis (Mtb)

Identifiers

PMID31680058
PMCPMC6915848
OpenAlexW2982627553

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.