Inducible costimulator (ICOS) is a marker for highly suppressive antigen-specific T cells sharing features of T"H17/T"H1 and regulatory T cells

J Allergy Clin Immunol 126(2):0 (2010) PMID 20624644

Background: CD4^+CD25^+ regulatory T (Treg) cells are involved in the downmodulation of numerous immune responses to pathogens, tumors, or allergens. Objective: In this study, we further characterized the nature of Treg cells that control skin inflammatory reactions to haptens. Methods: In a model of contact hypersensitivity to 2,4-dinitro-fluorobenzene, we have investigated the phenotype, the specificity, and the origin of Treg cells that modulate the priming of effector CD8^+ T cells responsible for the development of the pathology. Results: 2,4-Dinitrofluorobenzene immunization induced a population of CD4^+CD25^+ Treg cells that controlled CD8^+ T-cell effector responses in a hapten-specific manner in vivo. High levels of inducible costimulator (ICOS) expression defined a population of CD4^+CD25^+FoxP3^+ (forkhead box protein 3) Treg cells that presented superior suppressive activity. Importantly, ICOS^+ Treg cells were distinguishable from all other FoxP3^+ Treg cells by the expression of IL-10, IL-17, and IFN-@c. Hapten-specific Treg cells proliferating in response to their cognate antigen in vivo predominantly displayed a CD25^+FoxP3^+ICOS^+ phenotype. By using reporter mice, we showed that ICOS^+ Treg cells derived from the expansion of natural CD4^+FoxP3^+ Treg cells rather than generation of adaptive Treg cells. Furthermore, the generation of ICOS^+ Treg cells depended on innate cells rather than the effector CD8^+ T-cell population. Conclusion: Taken together, our data show that a population of CD4^+CD25^+FoxP3^+ T cells upregulates ICOS on in vivo sensitization and specifically suppresses hapten-reactive CD8^+ T cells both in vivo and in vitro.