The expression of PD-1 and its ligands increases in Leishmania infection and its blockade reduces the parasite burden

The expression of programmed cell death protein-1 (PD-1) and its ligands-PD-L1 and PD -L2-on T cells and macrophages', respectively, increases in Leishmania infection. The PD-1/PD-L1 interaction induces T cell anergy, T cell apoptosis and exhaustion, diversion of T cells toward TH2 and T-reg cells but inhibits M1 macrophage activities by suppression of nitric oxide (NO) and reactive oxygen species (ROS) production. These changes exacerbate Leishmania infection. As PD-L1-deficient, but not PD-L2-deficient, mice were protected against L. mexicana infection, differential roles have been proposed for PD-L1 and PD-L2 in mouse models of leishmaniasis. Blockade of PD-1/PD-L1 interaction in various in vitro and Leishmania-infected mouse, hamster and dog models enhanced IFN-gamma and NO production, reduced IL-10 and TGF-8 generation, promoted T cell proliferation and reduced parasite burden. Therefore, PD-1/PD-L1 blockade is being considered as a potential therapeutic strategy to restore protective immunity during leishmaniasis, particularly, in drug-resistant cases.

Automated summary

The expression of PD-1 and its ligands increase in Leishmania infection and lead to immune suppression. Blocking PD-1/PD-L1 interaction can enhance immune response and reduce parasite burden, making it a potential therapeutic strategy.