| Popis: |
IL-33 is an alarmin required for resistance to the parasiteToxoplasma gondii, but its role in innate resistance to this infection is unclear.T. gondiiinfection promotes increased stromal cell expression of IL-33 and levels of parasite replication correlate with IL-33 release. In response to infection, a subset of innate lymphoid cells (ILC) emerges composed of IL-33R+NK cells and ILC1s. In Rag-/-mice, where NK cells and ILC1 provide an innate mechanism of resistance toT. gondii, the loss of IL-33R reduced ILC responses and increased parasite replication. Furthermore, administration of IL-33 to Rag-/-mice resulted in a marked decrease in parasite burden, increased production of IFN-γ and the recruitment and expansion of inflammatory monocytes associated with parasite control. These protective effects of exogenous IL-33 were dependent on endogenous IL-12p40 and the ability of IL-33 to enhance ILC production of IFN-γ. These results highlight that IL-33 synergizes with IL-12 to promote ILC-mediated resistance toT. gondii. |
