Evidence map›Paper›PMID 41695367›Full record

ArticleFrontiers in oncology2026

Identification of a neoplastic Tfh-like cellular subset in a mouse model of angioimmunoblastic T cell lymphoma.

Saba Mohammaei, Jiyeon Lee, Antoine Bouchard, Evany Bernal Ballesteros, Nikoletta Diamantopoulos, Lifei Hou, Eileen Remold, Junhun Cho, Woong-Kyung Suh

Abstract read
In one paragraph

Article in Frontiers in oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Saba MohammaeiInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, QC, Canada.
Jiyeon LeeDepartment of Pathology, Samsung Medical Center, Seoul, Republic of Korea.
Antoine BouchardInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, QC, Canada.
Evany Bernal BallesterosInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, QC, Canada.
Nikoletta DiamantopoulosInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, QC, Canada.
Lifei HouEdelweiss Immune Inc, Brookline, MA, United States.
Eileen RemoldEdelweiss Immune Inc, Brookline, MA, United States.
Junhun ChoDepartment of Pathology, Samsung Medical Center, Seoul, Republic of Korea.
Woong-Kyung SuhInstitut de Recherches Cliniques de Montréal (IRCM), Montréal, QC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nodal T-follicular helper cell lymphoma, angioimmunoblastic type (nTFHL-AI, or AITL), is an aggressive peripheral T cell lymphoma without effective treatments. It has been shown that genetic and epigenetic changes lead to the expansion of neoplastic CD4 Methods: Through single-cell transcriptome analysis of Tfh-like cells isolated from the spontaneously arising AITL-like tumors in Results: DE Tfh cells expressed higher levels of Ki-67 and enhancer of zeste homolog 2 (EZH2) and proliferated more rapidly compared to other Tfh cells in an IL-18 and EZH2 dependent manner. Furthermore, DE Tfh cells engrafted better than non-DE Tfh cells and could cause B cell expansion when adoptively transferred into lymphopenic recipients. On the other hand, depletion of DE Tfh cells via Conclusions: Our study identified a pathogenic Tfh-like subset essential for AITL tumor progression in a mouse model and suggests that identifying and targeting a DE Tfh-like subset in AITL patients might be an effective strategy.

Indexed as

AITLangioimmunoblastic T cell lymphomaCXCR6EZH2IL-18RsanroqueTFHT follicular helper cell

Identifiers

PMID41695367
PMCPMC12900724

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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.