ADAP plays a pivotal role in CD4+ T cell activation but is only marginally involved in CD8+ T cell activation

The adhesion and degranulation promoting adaptor protein (ADAP) is a multifunctional scaffold involved in many different signaling pathways that are important for the function of T cells, including the inside-out and outside-in signaling of integrins, the activation of NF-B-k, and the subsequent production of proinflammatory cytokines (e.g., IFN-gamma and IL-2). Strikingly, despite its well-established role in T cells, previous studies did not distinguish between CD4(+) and CD8(+) T cells, and thus, it is unknown whether ADAP fulfills equally important functions in both T cell subsets. We show here that despite comparable ADAP expression levels in CD4(+) and CD8(+) T cells, their function is differentially dependent on ADAP. Whereas in vitro TCRstimulation experiments revealed that activation, proliferation, and adhesion are severely compromised in CD4(+) T cells lacking ADAP, their CD8(+) counterparts are hardly affected by ADAP deficiency. Accordingly, antigen-specific in vivo stimulation of adoptively transferred CD8(+) T cells during Listeria monocytogenes (Lm) and influenza A virus (IAV) infection revealed only moderate effects of ADAP deficiency in terms of CD8(+) T cell activation, proliferation, and differentiation, which, however, did not impair pathogen-specific immunity. Thus, we show for the first time that ADAP fulfills different functions in CD4(+) and CD8(+) T cells, with CD8(+) T cells being less dependent on ADAP. Our data identify ADAP as a potential molecular target for T cell subset-specific therapeutic interventions.