RT Journal Article SR Electronic T1 Differential Sensitivity to IL-12 Drives Sex-Specific Differences in the CD8+ T Cell Response to Infection JF ImmunoHorizons FD American Association of Immunologists SP 121 OP 132 DO 10.4049/immunohorizons.1800066 VO 3 IS 4 A1 Yee Mon, Kristel Joy A1 Goldsmith, Elizabeth A1 Watson, Neva B. A1 Wang, Jocelyn A1 Smith, Norah L. A1 Rudd, Brian D. YR 2019 UL http://www.immunohorizons.org/content/3/4/121.abstract AB It is well known that males and females respond differently to intracellular pathogens. Females mount a more robust immune response than males, which decreases their susceptibility to infection but comes at the cost of increasing immunopathology. However, the underlying basis for sex-specific differences in the CD8+ T cell response to infection remains poorly understood. In this study, we show that female CD8+ T cells have an intrinsic propensity to become short-lived effectors, whereas male CD8+ T cells give rise to more memory precursor effector cells after murine infection with either a virus (vaccinia virus) or bacteria (Listeria monocytogenes). Interestingly, we found that the propensity of female CD8+ T cells to form short-lived effectors is not because they respond to lower amounts of cognate Ag but rather because they have an enhanced capacity to respond to IL-12, which facilitates more effector cell differentiation at each round of cell division. Our findings provide key insights into the sex-based immunological differences that underlie variations in the susceptibility to infection in males and females.