PD-L1-deficient mice show that PD-L1 on T cells, antigen-presenting cells, and host tissues negatively regulates T cells

Abstract

Both positive and negative regulatory roles have been suggested for the B7 family member PD-L1(B7-H1). PD-L1 is expressed on antigen-presenting cells (APCs), activated T cells, and a variety of tissues, but the functional significance of PD-L1 on each cell type is not yet clear. To dissect the functions of PD-L1 in vivo , we generated PD-L1-deficient (PD-L1 –/– ) mice. CD4 + and CD8 + T cell responses were markedly enhanced in PD-L1 –/– mice compared with wild-type mice in vitro and in vivo . PD-L1 –/– dendritic cells stimulated greater wild-type CD4 + T cell responses than wild-type dendritic cells, and PD-L1 –/– CD4 + T cells produced more cytokines than wild-type CD4 + T cells in vitro , demonstrating an inhibitory role for PD-L1 on APCs and T cells. In vivo CD8 + T cell responses also were significantly enhanced, indicating that PD-L1 has a role in limiting the expansion or survival of CD8 + T cells. Studies using the myelin oligodendrocyte model of experimental autoimmune encephalomyelitis showed that PD-L1 on T cells and in host tissues limits responses of self-reactive CD4 + T cells in vivo . PD-L1 deficiency converted the 129S4/SvJae strain from a resistant to experimental autoimmune encephalomyelitis-susceptible strain. Transfer of encephalitogenic T cells from wild-type mice into PD-L1 –/– recipients led to exacerbated disease. Disease was even more severe in PD-L1 –/– recipients of PD-L1 –/– T cells. These results demonstrate that PD-L1 on T cells, APCs, and host tissue inhibits naïve and effector T cell responses and plays a critical role in T cell tolerance.