Androgen receptor-mediated CD8+ T cell stemness programs drive sex differences in antitumor immunity

Most non-reproductive human cancers exhibit sex differences, but the underlying immunological mechanism remains unknown. Yang et  al. identify that AR signaling accelerates the transition from stem cell-like CD8+ T cells to terminally exhausted CD8+ T cells in males, leading to sex-biased antitumor immunity, whereas AR signaling inhibition reprograms CD8+ T cells into a stem cell-like state to potentiate cancer immunother apy.
Source: Immunity - Category: Allergy & Immunology Authors: Tags: Article Source Type: research