Plasticity of the systemic inflammatory response to acute infection during critical illness: development of the riboleukogram

• Published in: PloS one 2008-02, Vol.3 (2), p.e1564-e1564
• Main Authors: McDunn, Jonathan E, Husain, Kareem D, Polpitiya, Ashoka D, Burykin, Anton, Ruan, Jianhua, Li, Qing, Schierding, William, Lin, Nan, Dixon, David, Zhang, Weixiong, Coopersmith, Craig M, Dunne, W Michael, Colonna, Marco, Ghosh, Bijoy K, Cobb, J Perren
• Format: Article
• Language: English
• Subjects: Abundance; Acute Disease; Analysis; Anesthesiology; Animals; Buffy coat; Clinical trials; Computational Biology/Systems Biology; Computer science; Critical Care and Emergency Medicine; Critical Illness; Cytokines; Data recovery; Diagnosis; Diagnostic Techniques, Respiratory System; DNA microarrays; Dynamical systems; Endotoxins; Engineering; Epidemiology; Gene expression; Gene Expression Profiling; Genes; Genetics and Genomics; Genomics; Health aspects; Heterogeneity; Humans; Illnesses; Immunology; Infections; Infectious Diseases; Inflammation; Inflammatory response; Injury analysis; Intensive care; Laboratory animals; Leukocytes; Mathematics; Medical diagnosis; Medical research; Methods; Mice; Microbiology; Minority & ethnic groups; Mortality; Oligonucleotide Array Sequence Analysis; Patients; Pneumonia; Pneumonia - diagnosis; Pneumonia, Ventilator-Associated; Principal components analysis; Ribonucleic acid; RNA; Sepsis; Studies; Surgery; Systemic Inflammatory Response Syndrome - diagnosis; Trachea; Transcription; Transcription, Genetic; Ventilation; Ventilators
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0001564

Diagnosis of acute infection in the critically ill remains a challenge. We hypothesized that circulating leukocyte transcriptional profiles can be used to monitor the host response to and recovery from infection complicating critical illness. A translational research approach was employed. Fifteen mice underwent intratracheal injections of live P. aeruginosa, P. aeruginosa endotoxin, live S. pneumoniae, or normal saline. At 24 hours after injury, GeneChip microarray analysis of circulating buffy coat RNA identified 219 genes that distinguished between the pulmonary insults and differences in 7-day mortality. Similarly, buffy coat microarray expression profiles were generated from 27 mechanically ventilated patients every two days for up to three weeks. Significant heterogeneity of VAP microarray profiles was observed secondary to patient ethnicity, age, and gender, yet 85 genes were identified with consistent changes in abundance during the seven days bracketing the diagnosis of VAP. Principal components analysis of these 85 genes appeared to differentiate between the responses of subjects who did versus those who did not develop VAP, as defined by a general trajectory (riboleukogram) for the onset and resolution of VAP. As patients recovered from critical illness complicated by acute infection, the riboleukograms converged, consistent with an immune attractor. Here we present the culmination of a mouse pneumonia study, demonstrating for the first time that disease trajectories derived from microarray expression profiles can be used to quantitatively track the clinical course of acute disease and identify a state of immune recovery. These data suggest that the onset of an infection-specific transcriptional program may precede the clinical diagnosis of pneumonia in patients. Moreover, riboleukograms may help explain variance in the host response due to differences in ethnic background, gender, and pathogen. Prospective clinical trials are indicated to validate our results and test the clinical utility of riboleukograms.