CD1d-independent regulation of NKT cell migration and cytokine production upon Listeria monocytogenes infection

Abstract

Natural killer T (NKT) cells are a unique T-cell population that is positively selected by CD1d-expressing cells. In this study, we examined the kinetics of conventional CD4 +TCRβ + and CD4 −TCRβ + cells along with various NKT cell populations from WT and CD1d KO mice after oral Listeria monocytogenes (Lm) infection at different time points in tissue compartments. We found that CD4 +TCRβ + cells expressing NK1.1 + (NKT) were constitutively expressed in the lung of both strains of mice, but disappeared after infection. In contrast, CD4 −TCRβ + NK1.1 + cells migrated to the spleen. Here, we demonstrated that endogenous IL-12 was predominantly expressed in the spleen of CD1d KO mice 2 days after infection, whereas IL-4 was predominantly expressed in the liver of WT mice. Higher levels of IFN-γ were expressed in MLN of CD1d KO but not in WT mice on day 5. Thus, tissue-specific ligands orchestrate the localization and activation of NKT cells to control immune response to Listeria, which may explain the difference in disease susceptibility.