Evidence map›Paper›PMID 42549226›Full record

ArticleJournal of asthma and allergy2026

Circulating TFH2 Cell Expansion and GZMK

Jiejun He, Yueqi Sun, Yang Chen, Yinyan Lai, Han Lei, Jianbo Shi, Wenxiang Gao

Abstract read
In one paragraph

Article in Journal of asthma and allergy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Jiejun He *Department of Otolaryngology, Otorhinolaryngology Hospital, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, People's Republic of China.
Yueqi Sun *Department of Otolaryngology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, People's Republic of China.
Yang ChenDepartment of Otolaryngology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, People's Republic of China.
Yinyan LaiDepartment of Otolaryngology, Otorhinolaryngology Hospital, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, People's Republic of China.
Han LeiDepartment of Otolaryngology, Otorhinolaryngology Hospital, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, People's Republic of China.
Jianbo ShiDepartment of Otolaryngology, Otorhinolaryngology Hospital, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, People's Republic of China.
Wenxiang GaoDepartment of Otolaryngology, Otorhinolaryngology Hospital, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, People's Republic of China.ORCID 0000-0002-5048-3907

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Allergic rhinitis (AR) is a prevalent condition characterized by an immunoglobulin E (IgE)-mediated immune response. T follicular helper (TFH) cells regulate B-cell differentiation and antibody production, and circulating TFH2 cells are closely associated with type 2 humoral immunity and IgE-related responses in AR. However, whether AR is marked by isolated TFH2 expansion or broader remodeling of circulating TFH (cTFH) subsets, including TFH1-related heterogeneity, remains unclear. Methods: A total of 56 participants were enrolled, including 39 patients with AR and 17 healthy controls (HC). Flow cytometry was performed in 36 patients with AR and 14 HC to quantify cTFH subsets and activation states. Single-cell RNA sequencing (scRNA-seq) was conducted in an independent exploratory cohort comprising 3 patients with AR and 3 HC to characterize TFH transcriptional heterogeneity, based on canonical transcriptional programs. Results: Flow cytometry demonstrated that cTFH2 cell frequencies were significantly increased in patients with AR and positively correlated with disease severity. Activated CCR7^low PD-1^high cTFH cells were also elevated, indicating enhanced TFH activation. Further scRNA-seq analysis identified six transcriptionally distinct TFH clusters, with TFH2-like transcriptional signatures enriched in patients with AR, consistent with flow cytometric findings. Notably, a GZMK Conclusion: This study demonstrates the expansion of cTFH2 and GZMK

Indexed as

allergic diseasesGZMKsingle-cell RNA sequencingT follicular helper cells

Identifiers

PMID42549226
PMCPMC13431438

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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.