TY - JOUR AU - Dey, Nidhi S. AU - Senaratne, Sujai AU - Somaratne, Vijani AU - Madarasinghe, Nayani P. AU - Seneviratne, Bimalka AU - Forrester, Sarah AU - Montes de Oca, Marcela AU - Reis, Luiza Campos AU - Moulik, Srija AU - Walrad, Pegine B. AU - Chatterjee, Mitali AU - Goto, Hiro AU - Wickremasinghe, Renu AU - Lagos, Dimitris AU - Kaye, Paul M. AU - Ranasinghe, Shalindra T1 - Early reduction in PD-L1 expression predicts faster treatment response in human cutaneous leishmaniasis PY - 2024/03/01/ AB - Cutaneous leishmaniasis (CL) is caused by Leishmania donovani in Sri Lanka. Pentavalent antimonials (e.g., sodium stibogluconate [SSG]) remain first-line drugs for CL with no new effective treatments emerging. We studied whole blood and lesion transcriptomes from Sri Lankan patients with CL at presentation and during SSG treatment. From lesions but not whole blood, we identified differential expression of immune-related genes, including immune checkpoint molecules, after onset of treatment. Using spatial profiling and RNA-FISH, we confirmed reduced expression of programmed death-ligand 1 (PD-L1) and indoleamine 2,3-dioxygenase 1 (IDO1) proteins on treatment in lesions of a second validation cohort and further demonstrated significantly higher expression of these checkpoint molecules on parasite-infected compared with noninfected lesional CD68+ monocytes and macrophages. Crucially, early reduction in PD-L1 but not IDO1 expression was predictive of rate of clinical cure (HR = 4.88) and occurred in parallel with reduction in parasite load. Our data support a model whereby the initial anti–leishmanial activity of antimonial drugs alleviates checkpoint inhibition on T cells, facilitating immune-drug synergism and clinical cure. Our findings demonstrate that PD-L1 expression can be used as a predictor of rapidity of clinical response to SSG treatment in Sri Lanka and support further evaluation of PD-L1 as a host-directed therapeutic in leishmaniasis. JF - The Journal of Clinical Investigation JA - J Clin Invest SN - 0021-9738 DO - 10.1172/JCI142765 VL - 131 IS - 22 UR - https://doi.org/10.1172/JCI142765 PB - The American Society for Clinical Investigation ER -