转录组
败血症
表型
单核细胞
先天免疫系统
免疫系统
医学
免疫学
生物
生物信息学
基因
基因表达
遗传学
作者
Evan L. Barrios,Jaimar C. Rincon,Micah L. Willis,Valerie E. Polcz,Jack R. Leary,Dijoia B. Darden,Jeremy A. Balch,Shawn D. Larson,Tyler J. Loftus,Alicia M. Mohr,Shannon M. Wallet,Maigan A. Brusko,Leandro Balzano‐Nogueira,Guoshuai Cai,Ashish K. Sharma,Gilbert R. Upchurch,Michael P. Kladde,Clayton E. Mathews,Robert Maile,Lyle L. Moldawer
出处
期刊:Shock
[Lippincott Williams & Wilkins]
日期:2024-05-02
卷期号:62 (2): 208-216
标识
DOI:10.1097/shk.0000000000002379
摘要
Postsepsis early mortality is being replaced by survivors who experience either a rapid recovery and favorable hospital discharge or the development of chronic critical illness with suboptimal outcomes. The underlying immunological response that determines these clinical trajectories remains poorly defined at the transcriptomic level. As classical and nonclassical monocytes are key leukocytes in both the innate and adaptive immune systems, we sought to delineate the transcriptomic response of these cell types. Using single-cell RNA sequencing and pathway analyses, we identified gene expression patterns between these two groups that are consistent with differences in TNF-α production based on clinical outcome. This may provide therapeutic targets for those at risk for chronic critical illness in order to improve their phenotype/endotype, morbidity, and long-term mortality.
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