Evidence map›Paper›PMID 40976713›Full record

ReviewThe FEBS journal2026

Lung organoids as a human system for Mycobacteria infection modeling and drug testing.

Stephen Adonai Leon-Icaza, Romain Vergé, Raoul Mazars, Laurence Berry, Céline Cougoule

Abstract readReview
In one paragraph

Review in The FEBS journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Human lung organoids model for assessing host response toFrontiers in cellular and infection microbiology · 2026
    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

5 authors.

Stephen Adonai Leon-IcazaInstitut de Pharmacologie et Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, France.
Romain VergéInstitut de Pharmacologie et Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, France.
Raoul MazarsInstitut de Pharmacologie et Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, France.
Laurence BerryLaboratory of Pathogen Host Interactions (LPHI), Université Montpellier, CNRS, France.
Céline CougouleInstitut de Pharmacologie et Biologie Structurale (IPBS), Université de Toulouse, CNRS, UPS, France.ORCID 0000-0002-6795-5448

Funding

Agence Nationale de Recherches sur le Sida et les Hépatites Virales 21402; AO 2021-2 CSS 11Association Grégory Lemarchal RF20210502852/1/1/48Association Grégory Lemarchal RF20230503250Association Vaincre la Mucoviscidose RF20210502852/1/1/48Association Vaincre la Mucoviscidose RF20230503250HORIZON EUROPE Health 101080462
6 · The paper itself

Abstract

Mycobacterial infections remain a global public health challenge. Each year, high rates of morbidity and mortality worldwide are a consequence of chronic respiratory infections due to Mycobacteria. According to the World Health Organization (WHO), in 2023, 10.8 million individuals fell ill with Mycobacterium tuberculosis (Mtb), resulting in an estimated 1.25 million deaths. This positions tuberculosis (TB) as the leading cause of death from a single pathogen worldwide after the coronavirus disease (COVID-19) pandemic. On the other hand, the cases of people affected by nontuberculous mycobacteria (NTM) have risen globally, but the precise incidence and prevalence of both pulmonary and extrapulmonary disease remain unknown. In Europe, nontuberculous mycobacterial pulmonary diseases affect between 0.2 and 2.9 per 100 000 individuals, mainly patients with cystic fibrosis (CF) and non-CF bronchiectasis. The diagnosis and treatment of mycobacterial infections are challenging and complex, frequently requiring long-duration treatments with several antibiotics, which in most cases leads to poor patient outcomes. As the role of immune cells has been extensively assessed, in this Review, we summarize the current knowledge about the contribution of epithelial cells in the early steps of Mycobacteria infections. Additionally, we describe how human lung organoid technology provides new tools to better understand host-Mycobacteria interactions in the airways and test new therapeutic targets.

Indexed as

LungMycobacterium Infections, NontuberculousOrganoidsCOVID-19HumansMycobacterium tuberculosisSARS-CoV-2airway defense mechanismshost‐directed therapiesinfection modelinglung organoidsMycobacteria

Identifiers

PMID40976713
PMCPMC12998197

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.