Autoimmunity and organ transplant rejection affect over 25 million Americans, and together have an economic impact of over 100 billion dollars per year. These inflammatory diseases result from a breakdown of the intrinsic regulatory pathways that limit T cell activation and differentiation, and from a failure of regulatory T cells (Treg) t extrinsically suppress conventional T cell (Tconv) proliferation and effector function. Our work during the last two funding periods has focused on the role of cyclin-dependent kinases in T cell differentiation, anergy and tolerance. Our work established critical roles for CDK2 and its inhibitor p27kip1 in controlling the balance between immunity and tolerance. We showed that mice with a germline deletion of CDK2 accept cardiac allografts under conditions that lead to rejection in wild-type recipients, while mice lacking p27kip1 are highly resistant to tolerance induced by costimulatory blockade. Surprisingly, these factors do not operate through regulation of T cell cycle progression. Instead, we found that CDK2 activity promotes T helper differentiation, and that CDK2-deficient Treg exhibit a gain of suppressive activity. In this renewal application, we will explore this exciting new role for the CDK2 pathway in the control of regulatory T cell function, focused mainly by our findings that Foxp3 is phosphorylated and targeted for degradation by CDK2, and that dysregulated CDK2 activity opposes the induction and stability of Foxp3+ Treg. The proposed work will forward our basic understanding of how Foxp3 and regulatory T cell function is regulated, and will also have important therapeutic implications. Small molecule CDK antagonists are currently in phase I clinical trials, and based on our findings, could potentially be used to promote regulatory T cell function and tolerance in autoimmune and organ transplant patients.
Autoimmunity and organ transplant rejection affect over 25 million Americans, and together have an economic impact of over 100 billion dollars per year. These inflammatory diseases result from a break down of the 'checks and balances'that normally limit activation of the cells of the immune system. We have identified an unexpected and exciting link between a basic biochemical pathways involved in regulating cell growth, called the cyclin-dependent kinase cascade, and the stability of a factor called Foxp3. This molecule is required to guard against autoimmunity and chronic inflammation, and we have evidence that the cyclin-dependent kinase pathway works against the ability of Foxp3 to do its job. This work will have important therapeutic implications, as small molecule cyclin-dependent kinase inhibitors are currently in phase I clinical trials. Based on our findings, these drugs coul potentially be used to promote Foxp3 function, inhibit inflammation, and reverse immunopathologic disease in autoimmune and organ transplant patients.
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