PT  - JOURNAL ARTICLE
AU  - Maurice, Nicholas J
AU  - Dalzell, Talia S
AU  - Jarjour, Nicholas N
AU  - DePauw, Taylor A
AU  - Jameson, Stephen C
TI  - Steady-state, therapeutic, and helminth-induced IL-4 compromise protective CD8 T cell bystander activation
AID  - 10.1101/2024.06.10.598293
DP  - 2024 Jan 01
TA  - bioRxiv
PG  - 2024.06.10.598293
4099  - http://biorxiv.org/content/early/2024/06/12/2024.06.10.598293.short
4100  - http://biorxiv.org/content/early/2024/06/12/2024.06.10.598293.full
AB  - Memory CD8 T cells (Tmem) can be activated into innate-like killers by cytokines like IL-12, IL-15, and/or IL-18; but mechanisms regulating this phenomenon (termed bystander activation) are not fully resolved. We found strain-intrinsic deficiencies in bystander activation using specific pathogen-free mice, whereby basal IL-4 signals antagonize IL-18 sensing. We show that therapeutic and helminth-induced IL-4 impairs protective bystander-mediated responses against pathogens. However, this IL-4/IL-18 axis does not completely abolish bystander activation but rather tunes the expression of direct versus indirect mediators of cytotoxicity (granzymes and interferon-γ, respectively). We show that antigen-experience overrides strain-specific deficiencies in bystander activation, leading to uniform IL-18 receptor expression and enhanced capacity for bystander activation/cytotoxicity. Our data highlight that bystander activation is not a binary process but tuned/deregulated by other cytokines that are elevated by contemporaneous infections. Further, our findings underscore the importance of antigen-experienced Tmem to dissect the contributions of bystander Tmem in health and disease.Competing Interest StatementThe authors have declared no competing interest.