急性呼吸窘迫综合征
免疫系统
医学
细胞
免疫学
内科学
肺
生物
遗传学
作者
Eric D. Morrell,Sarah E. Holton,Alice Wiedeman,Susanna Harju-Baker,Mallorie A. Mitchem,Victoria Dmyterko,Zoie Franklin,A. Garay,Ian B. Stanaway,Ted Liu,Neha A. Sathe,F. Linzee Mabrey,Renee D. Stapleton,Uma Malhotra,Cate Speake,Jessica A. Hamerman,Sudhakar Pipavath,Laura Evans,Pavan K. Bhatraju,Sihui Long,Mark M. Wurfel,Carmen Mikacenic
标识
DOI:10.1165/rcmb.2024-0201oc
摘要
The relationship between the Programmed Death-Ligand 1 (PD-L1)/Programmed Death-1 (PD-1) pathway, lung inflammation, and clinical outcomes in acute respiratory distress syndrome (ARDS) is poorly understood. We sought to determine whether PD-L1/PD-1 in the lung or blood is associated with ARDS and associated severity. We measured soluble PD-L1 (sPD-L1) in plasma and lower respiratory tract samples (ARDS1 (n = 59) and ARDS2 (n = 78)) or plasma samples alone (ARDS3 (n = 149)) collected from subjects with ARDS and tested for associations with mortality using multiple regression. We used mass cytometry to measure PD-L1/PD-1 expression and intracellular cytokine staining in cells isolated from bronchoalveolar lavage fluid (BALF) (n = 18) and blood (n = 16) from critically-ill subjects with or without ARDS enrolled from a fourth cohort. Higher plasma levels of sPD-L1 were associated with mortality in ARDS1, ARDS2, and ARDS3. In contrast, higher levels of sPD-L1 in the lung were either not associated with mortality (ARDS2) or were associated with survival (ARDS1). Alveolar PD-1
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