Evidence mapPaperPMID 41514641Full record

ArticleCancers2025

Colorectal Air-Liquid Interface Organoids Preserve Tumour-Immune Architecture and Reveal Local Treg Expansion After PD-1 Blockade.

Laura Córdoba, Francisco J Cueto, Ramón Cantero-Cid, Rebeca Abad-Moret, Esteban Díaz, Jaime Álvarez-Benayas, Jesús Fernández-Felipe, Jesús Jiménez-Rodríguez, Daniel Arvelo-Rosario, Pablo Mata-Martínez and 16 more

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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

26 authors.

Laura CórdobaBiobank Platform, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0001-5549-4093
Francisco J CuetoThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0002-7457-9583
Ramón Cantero-CidDigestive Surgery Service, La Paz University Hospital, 28046 Madrid, Spain.
Rebeca Abad-MoretDigestive Surgery Service, La Paz University Hospital, 28046 Madrid, Spain.
Esteban DíazDigestive Surgery Service, La Paz University Hospital, 28046 Madrid, Spain.
Jaime Álvarez-BenayasARIES Research Group, Universidad Antonio de Nebrija, 28248 Madrid, Spain.ORCID 0000-0002-1922-7681
Jesús Fernández-FelipeThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Jesús Jiménez-RodríguezBiobank Platform, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Daniel Arvelo-RosarioThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Pablo Mata-MartínezThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Marina Arranz-ÁlvarezBiobank Platform, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Yaiza Pedroche-JustBiobank Platform, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Sandra Nieto-TorreroBiobank Platform, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Jaime Valentín-QuirogaThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Verónica Terrón-ArcosThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Jaime Fernández-PascualThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Paloma Gómez-CampeloBiobank Platform, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Nieves Cubo-MateoARIES Research Group, Universidad Antonio de Nebrija, 28248 Madrid, Spain.ORCID 0000-0002-0717-3049
Olivia Fernández-MedinaThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Laura Hurtado-NavarroThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Gonzalo Sáenz de Santa MaríaThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Julia Del Prado-MonteroThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Agustín L SantosBiobank Platform, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.
Roberto Lozano-RodríguezThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0003-0093-9707
Carlos Del FresnoThe Innate Immune Response Group, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0003-1771-7254
Eduardo López-CollazoBiobank Platform, IdiPAZ, La Paz University Hospital, 28046 Madrid, Spain.ORCID 0000-0003-1957-877X

Funding

European Biobanking Infrastructure 829 (BBMRI-ERIC) PT20/00004Instituto de Salud Carlos III (ISCIII) FORT23/00006Instituto de Salud Carlos III (ISCIII) PI21/00869
6 · The paper itself

Abstract

BACKGROUND/

objectivesInteractions between colorectal tumours and their immune microenvironment critically influence disease progression and response to immunotherapy. However, most organoid systems fail to preserve the complex architecture and immune composition of the original tissue. Here, we applied the air-liquid interface (ALI) organoid model to paired tumour and perilesional colon tissues from colorectal cancer patients to evaluate its ability to retain immune and genetic features and to reproduce responses to chemotherapy and immune checkpoint blockade.

methodsFresh human tumour and matched healthy colon tissues were processed to generate ALI organoids. Their histological organization, immune cell composition (including CD45

resultsALI organoids faithfully preserved the three-dimensional architecture, native immune infiltrates, and somatic mutational landscape of the source tissues. Importantly, upon PD-1 blockade with nivolumab, ALI organoids consistently exhibited a local expansion of regulatory T cells (Tregs), a phenomenon that could contribute to adaptive immune resistance. This response was not reproduced in PBMC-Matrigel co-culture systems, highlighting the importance of preserving endogenous tumour-immune interactions.

conclusionsPatient-derived ALI organoids represent a physiologically relevant platform that conserves key structural, immunological, and genomic hallmarks of colorectal cancer. By capturing clinically relevant immune remodeling events, such as Treg expansion following PD-1 blockade, this model provides a powerful tool for dissecting tumour-immune interactions.

Indexed as

air–liquid interface organoidsimmune infiltratesMatrigel organoidsnivolumabregulatory T cells

Identifiers

PMID41514641
PMCPMC12784706

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.