Sign in
ImmunologybioRxiv
Preprint

Transcriptional reprogramming of tumor-infiltrating T cells during PD-1 blockade revealed through gene regulatory network and trajectory inference in squamous cell carcinoma

Roger Casals-FranchiD, Jordi Villà­-FreixaiD, Lara NonelliD, Adrián López García de LomanaiD

Abstract

Understanding the tumor microenvironment is crucial for optimizing anti-cancer immune responses. At single-cell resolution, trajectory inference methods can reconstruct the dynamic transitions between cell states during differentiation. Immune checkpoint blockade (ICB) therapies, such as PD-1/PD-L1 inhibitors, are used across multiple cancers, including non-melanoma skin cancers (NMSCs), yet the transcriptional mechanisms that shape T cell responses in this context remain unclear. Here, we analyzed a publicly available squamous cell carcinoma (SCC) single-cell RNA-seq dataset comprising 25,581 tumor-infiltrating T-cell profiles to map differentiation trajectories before and after anti-PD-1 therapy. In CD8+ T cells, therapy enhanced the transition from memory to activated states, prominently involving IL-12-associated pathways, and revealed a distinct memory-to-exhaustion trajectory driven by EOMES and TCF7 regulatory activity. Gene regulatory network inference further revealed therapy-induced transcriptional rewiring distinguishing precursor exhausted (Tpex) from terminally exhausted (Tex) states. CD4+ T cell populations also underwent substantial reshaping, with trajectory and functional analyses highlighting therapy-driven programs that enhanced CXCL13+ Tfh responses while generating fewer but more transcriptionally active Tregs. Together, these findings reveal a dual remodeling of helper and cytotoxic T cell compartments upon PD-1 blockade, define key transcriptional regulators controlling cell-state transitions, and identify potential molecular targets and biomarkers to predict and enhance treatment response.

PDFDOI

02 /Specification & Classification

Click any tag to browse matching papers

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.