Evidence map›Paper›PMID 40185986›Full record

ArticleCommunications biology2025

Single-cell transcriptional responses of T cells during microsporidia infection.

Yunlin Tang, Lu Cao, Jiangyan Jin, Tangxin Li, Yebo Chen, Yishan Lu, Tian Li, Louis M Weiss, Guoqing Pan, Jialing Bao and 1 more

Abstract read
In one paragraph

Article in Communications biology, 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. 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

11 authors.

Yunlin TangState Key Laboratory of Resource Insects, Southwest University, Chongqing, China.ORCID http://orcid.org/0009-0006-3721-0169
Lu CaoState Key Laboratory of Resource Insects, Southwest University, Chongqing, China.
Jiangyan JinState Key Laboratory of Resource Insects, Southwest University, Chongqing, China.
Tangxin LiState Key Laboratory of Resource Insects, Southwest University, Chongqing, China.
Yebo ChenState Key Laboratory of Resource Insects, Southwest University, Chongqing, China.
Yishan LuState Key Laboratory of Resource Insects, Southwest University, Chongqing, China.
Tian LiState Key Laboratory of Resource Insects, Southwest University, Chongqing, China.
Louis M WeissDepartment of Pathology, Albert Einstein College of Medicine, New York, NY, USA.
Guoqing PanState Key Laboratory of Resource Insects, Southwest University, Chongqing, China.
Jialing BaoState Key Laboratory of Resource Insects, Southwest University, Chongqing, China. baojl@swu.edu.cn.ORCID http://orcid.org/0000-0002-0686-3435
Zeyang ZhouState Key Laboratory of Resource Insects, Southwest University, Chongqing, China. zyzhou@swu.edu.cn.ORCID http://orcid.org/0000-0003-2296-0742

Funding

National Natural Science Foundation of China (National Science Foundation of China) 31802141Southwest University (SWU) SWU-XDJH202322Southwest University (SWU) XDJK2020B005
6 · The paper itself

Abstract

T cells have been reported to play critical roles in preventing of microsporidia dissemination. However, there roles and functions of each subset remain unclear. Here in the study, we performed a thorough analysis of murine splenic T-cell response analysis via single-cell RNA sequencing during microsporidia E. cuniculi infection. We demonstrated that Type I T helper (Th1) cells, T follicular helper (Tfh) cells, effector CD8 + T cells and proliferating CD8 + T cells were activated and expanded after infection. Activated Th1 cells and Tfh cells presented significantly upregulated gene expression of Ifng and Il21, respectively. A subcluster of Th1 cells with high Csf1 expression was detected after infection. Subsets of activated CD8 + T cells were markedly enriched with high expression of cytotoxic-function related genes such as Gzma and Gzmb, whereas some active CD8 T cells were enriched with proliferation-function related genes Mki67 and Stmn1. Other subsets of T cells including NK T cells, Myb+ T cells, γδ T cells and Cxcr6+ T cells, were also analyzed in this study yet no expansion was observed. In summary, our findings provide in-depth and comprehensive insights into T-cell responses during microsporidia infection, which will be valuable for further investigations.

Indexed as

MicrosporidiaMicrosporidiosisAnimalsCD8-Positive T-LymphocytesLymphocyte ActivationMiceMice, Inbred C57BLSingle-Cell Analysis

Identifiers

PMID40185986
PMCPMC11971339

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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.