Evidence map›Paper›PMID 37143660›Full record

ArticleFrontiers in immunology2023

Deciphering the maturation of tertiary lymphoid structures in cancer and inflammatory diseases of the digestive tract using imaging mass cytometry.

Marion Le Rochais, Patrice Hémon, Danivanh Ben-Guigui, Soizic Garaud, Christelle Le Dantec, Jacques-Olivier Pers, Divi Cornec, Arnaud Uguen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

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  20. Maturation of Tertiary Lymphoid Structures.Methods in molecular biology (Clifton, N.J.) · 2025
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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.

Marion Le RochaisLymphocytes B, Autoimmunité et Immunothérapies (LBAI), Unité Mixte de Recherche (UMR)51227, Univ Brest, Inserm, Brest, France.
Patrice HémonLymphocytes B, Autoimmunité et Immunothérapies (LBAI), Unité Mixte de Recherche (UMR)51227, Univ Brest, Inserm, Brest, France.
Danivanh Ben-GuiguiLymphocytes B, Autoimmunité et Immunothérapies (LBAI), Unité Mixte de Recherche (UMR)51227, Univ Brest, Inserm, Brest, France.
Soizic GaraudLymphocytes B, Autoimmunité et Immunothérapies (LBAI), Unité Mixte de Recherche (UMR)51227, Univ Brest, Inserm, Brest, France.
Christelle Le DantecLymphocytes B, Autoimmunité et Immunothérapies (LBAI), Unité Mixte de Recherche (UMR)51227, Univ Brest, Inserm, Brest, France.
Jacques-Olivier PersLymphocytes B, Autoimmunité et Immunothérapies (LBAI), Unité Mixte de Recherche (UMR)51227, Univ Brest, Inserm, Brest, France.
Divi CornecLymphocytes B, Autoimmunité et Immunothérapies (LBAI), Unité Mixte de Recherche (UMR)51227, Univ Brest, Inserm, Brest, France.
Arnaud UguenLymphocytes B, Autoimmunité et Immunothérapies (LBAI), Unité Mixte de Recherche (UMR)51227, Univ Brest, Inserm, Brest, France.
Université de Bretagne Occidentale · FRCentre Hospitalier Régional Universitaire de Brest · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent inflammation can promote the development of tertiary lymphoid structures (TLS) within tissues resembling secondary lymphoid organs (SLO) such as lymph nodes (LN). The composition of TLS across different organs and diseases could be of pathophysiological and medical interest. In this work, we compared TLS to SLO in cancers of the digestive tract and in inflammatory bowel diseases. Colorectal and gastric tissues with different inflammatory diseases and cancers from the department of pathology of CHU Brest were analyzed based on 39 markers using imaging mass cytometry (IMC). Unsupervised and supervised clustering analyses of IMC images were used to compare SLO and TLS. Unsupervised analyses tended to group TLS per patient but not per disease. Supervised analyses of IMC images revealed that LN had a more organized structure than TLS and non-encapsulated SLO Peyer's patches. TLS followed a maturation spectrum with close correlations between germinal center (GC) markers' evolution. The correlations between organizational and functional markers made relevant the previously proposed TLS division into three stages: lymphoid-aggregates (LA) (CD20+CD21-CD23-) had neither organization nor GC functionality, non-GC TLS (CD20+CD21+CD23-) were organized but lacked GC's functionality and GC-like TLS (CD20+CD21+CD23+) had GC's organization and functionality. This architectural and functional maturation grading of TLS pointed to differences across diseases. TLS architectural and functional maturation grading is accessible with few markers allowing future diagnostic, prognostic, and predictive studies on the value of TLS grading, quantification and location within pathological tissues in cancers and inflammatory diseases.

Indexed as

NeoplasmsTertiary Lymphoid StructuresGastrointestinal TractHumansImage CytometryPrognosiscancerHyperionimaging mass cytometryinflammationtertiary lymphoid structures

Identifiers

PMID37143660
PMCPMC10151544
OpenAlexW4366293315

What OpenQuestion 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 OpenQuestion graph.