Critical role of OX40/OX40L in ILC2-mediated activation of CD4+ T cells during respiratory syncytial virus infection in mice

CD4(+)T cells are crucial cellular source of type 2 cytokines and responsible for RSV-induced asthma-like symptoms and asthma exacerbations. However, the mechanism for regulating the activation of CD4(+)T cells during RSV infection is not clear completely. We show in this study that infection with RSV may induce an expansion and activation of CD4(+)T cells in the lungs of BALB/c mice. RSV-induced CD4(+)T cell expansion and activation seems to depend upon the pulmonary group 2 innate lymphoid cells (ILC2s), since adoptive transfer of lung ILC2s can enhance not only the numbers of CD4(+)T cells but also the cytokine production by CD4(+)T cells. Interestingly, blockade of the contact between ILC2s and CD4(+)T cells, may significantly diminish the CD4(+)T cell expansion and cytokine production, suggesting that membrane molecules may be involved in ILC2-regulated CD4(+)T cell activation. In fact, infection with RSV resulted in an increase in the numbers of OX40(+) CD4(+)T cells as well as OX40L(+)ILC2s in the lungs of mice. Moreover, the mRNA expressions of OX40 and OX40L as well as the levels of OX40 and OX40L proteins in the lung CD4(+)T cells and ILC2s were elevated respectively. When coculture of CD4(+)T cells with ILC2s in the presence of anti-OX40L antibody, the cytokine productions by CD4(+)T cells were reduced markedly, suggesting that lung ILC2s may regulate RSV-induced CD4(+)T cell expansion and activation perhaps via OX40/OX40L interaction.