The SKI proto-oncogene restrains the resident CD103 + CD8 + T cell response in viral clearance

Acute viral infection causes illness and death. In addition, an infection often results in increased susceptibility to a secondary infection, but the mechanisms behind this susceptibility are poorly understood. Since its initial identification as a marker for resident memory CD8 + T cells in barrier tissues, the function and regulation of CD103 integrin (encoded by ITGAE gene) have been extensively investigated. Nonetheless, the function and regulation of the resident CD103 + CD8 + T cell response to acute viral infection remain unclear. Although TGFβ signaling is essential for CD103 expression, the precise molecular mechanism behind this regulation is elusive. Here, we reveal a TGFβ–SKI–Smad4 pathway that critically and specifically directs resident CD103 + CD8 + T cell generation for protective immunity against primary and secondary viral infection. We found that resident CD103 + CD8 + T cells are abundant in both lymphoid and nonlymphoid tissues from uninfected mice. CD103 acts as a costimulation signal to produce an optimal antigenic CD8 + T cell response to acute viral infection. There is a reduction in resident CD103 + CD8 + T cells following primary infection that results in increased susceptibility of the host to secondary infection. Intriguingly, CD103 expression inversely and specifically correlates with SKI proto-oncogene (SKI) expression but not R-Smad2/3 activation. Ectopic expression of SKI restricts CD103 expression in CD8 + T cells in vitro and in vivo to hamper viral clearance. Mechanistically, SKI is recruited to the Itgae loci to directly suppress CD103 transcription by regulating histone acetylation in a Smad4-dependent manner. Our study therefore reveals that resident CD103 + CD8 + T cells dictate protective immunity during primary and secondary infection. Interfering with SKI function may amplify the resident CD103 + CD8 + T cell response to promote protective immunity.