CD40L expression by CD4 but not CD8 T cells regulates antiviral immune responses in acute LCMV infection in mice.

CD40-CD40 ligand (CD40L) signaling plays multiple indispensable roles in cellular and humoral immunity. Impaired memory T-cell responses in the absence of CD40L have been well documented, but the requirement of this interaction for efficient priming of CD8 T cells especially under inflammatory conditions has been under debate. In contrast to previous publications, we report here that virus-specific CD8 T-cell responses as well as viral clearance are affected not only in the memory but also in the effector phase in CD40L mice infected with lymphocytic choriomeningitis virus (LCMV) Armstrong strain. Interestingly, a considerable part of the LCMV-specific effector and memory T cells consists of CD40L CD8 T cells. However, deficiency of CD40L in CD8 T cells did influence neither the quantity nor the quality of primary T-cell responses in LCMV infection. Virus-specific CD8 T cells in conditional knockout mice, with a selective deletion of the CD40L in CD8 T cells, were fully functional regarding cytokine production and efficient pathogen clearance. Thus, our results unambiguously demonstrate that while CD40L is critical to generate effective primary CD8 T-cell responses also under inflammatory conditions, CD40L expression by CD8 T cells themselves is dispensable in acute LCMV infection.