| Literature DB >> 32432714 |
Sebastian Wurster1, Prema Robinson1, Nathaniel D Albert1, Jeffrey J Tarrand2, Marisa Goff3, Muthulekha Swamydas4, Jean K Lim3, Michail S Lionakis4, Dimitrios P Kontoyiannis1.
Abstract
Pharmacological immune checkpoint blockade has revolutionized oncological therapies, and its remarkable success has sparked interest in expanding checkpoint inhibitor therapy in infectious diseases. Herein, we evaluated the efficacy of programmed cell death protein 1 (PD-1) blockade in a murine invasive pulmonary aspergillosis model. We found that, compared with isotype-treated infected control mice, anti-PD-1-treated mice had improved survival, reduced fungal burden, increased lung concentrations of proinflammatory cytokines and neutrophil-attracting chemokines, and enhanced pulmonary leukocyte accumulation. Furthermore, combined treatment with anti-PD-1 and caspofungin resulted in a significant survival benefit compared with caspofungin or anti-PD-1 therapy alone, indicating a synergistic effect between PD-1 inhibitors and immunomodulatory antifungal agents. Published by Oxford University Press for the Infectious Diseases Society of America 2020.Entities:
Keywords: Antifungals; Checkpoint inhibitors; cytokines; immunotherapy; invasive aspergillosis
Year: 2020 PMID: 32432714 PMCID: PMC7430165 DOI: 10.1093/infdis/jiaa264
Source DB: PubMed Journal: J Infect Dis ISSN: 0022-1899 Impact factor: 5.226