The transcription factor Helios restrains the anti-tumor capacity of CD8+ T cells
Year: 2025
Type: article
Abstract: Immunotherapy has revolutionized cancer treatment, but it lacks efficacy in a sizable fraction of patients. Therefore, understanding the transcriptional networks that limit CD8 + T cell anti-tumor responses is fundamental. Here, we show that the transcription factor Helios is induced in tumor-infiltrating CD8 + T cells in human and murine cancer. Genetic deletion of Helios in CD8 + T cells reduces tumor growth, decreases the number of intratumoral terminally exhausted CD8 + T cells, and increases the frequency of cells with a transcriptional profile indicative of progenitor capacity. These changes are associated with increased chromatin accessibility in loci encoding stemness-related genes. The combination of Helios and PD-1 deficiencies robustly improves the anti-tumoral capacity of CD8 + T cells. A Helios inhibitor, identified in a small-molecule screen, improves the anti-tumoral effects of PD-1 deficiency. These results demonstrate that Helios represents a therapeutic target that can boost anti-cancer immunotherapy.
Source: Cell Reports
Authors: Rosa M. Rubio, Gerardo Suárez-Rojas, Adrián Albarrán-Godínez, Saraí G. De León-Rodríguez, Cristina Aguilar-Flores, Marco Fonseca-Montaño, Michelle Téllez-Sütterlin, Sofia V. de los Santos-Carmona, Karla Guzmán-Barrenechea, Fernando Candanedo-González, Enrique Soto-Perez-de-Celis, Laura Gómez-Romero, Diego Cortez, Marysol González-Yañez, Laura C. Bonifaz, Iris K. Madera-Salcedo, José C. Crispín, Florencia Rosetti
Language: English
Subfield: Oncology
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $5,620
OpenAlex ID: W4417256432
