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A time-resolved meta-analysis of consensus gene expression profiles during human T-cell activation.

Authors :
Rade M
Böhlen S
Neuhaus V
Löffler D
Blumert C
Merz M
Köhl U
Dehmel S
Sewald K
Reiche K
Source :
Genome biology [Genome Biol] 2023 Dec 14; Vol. 24 (1), pp. 287. Date of Electronic Publication: 2023 Dec 14.
Publication Year :
2023

Abstract

Background: The coordinated transcriptional regulation of activated T-cells is based on a complex dynamic behavior of signaling networks. Given an external stimulus, T-cell gene expression is characterized by impulse and sustained patterns over the course. Here, we analyze the temporal pattern of activation across different T-cell populations to develop consensus gene signatures for T-cell activation.<br />Results: Here, we identify and verify general biomarker signatures robustly evaluating T-cell activation in a time-resolved manner. We identify time-resolved gene expression profiles comprising 521 genes of up to 10 disjunct time points during activation and different polarization conditions. The gene signatures include central transcriptional regulators of T-cell activation, representing successive waves as well as sustained patterns of induction. They cover sustained repressed, intermediate, and late response expression rates across multiple T-cell populations, thus defining consensus biomarker signatures for T-cell activation. In addition, intermediate and late response activation signatures in CAR T-cell infusion products are correlated to immune effector cell-associated neurotoxicity syndrome.<br />Conclusion: This study is the first to describe temporally resolved gene expression patterns across T-cell populations. These biomarker signatures are a valuable source, e.g., monitoring transcriptional changes during T-cell activation with a reasonable number of genes, annotating T-cell states in single-cell transcriptome studies, or assessing dysregulated functions of human T-cell immunity.<br /> (© 2023. The Author(s).)

Details

Language :
English
ISSN :
1474-760X
Volume :
24
Issue :
1
Database :
MEDLINE
Journal :
Genome biology
Publication Type :
Academic Journal
Accession number :
38098113
Full Text :
https://doi.org/10.1186/s13059-023-03120-7