期刊
IMMUNITY
卷 43, 期 6, 页码 1199-1211出版社
CELL PRESS
DOI: 10.1016/j.immuni.2015.11.003
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类别
资金
- La Caixa'' Foundation
- NHMRC
- Stanford Child Health Research Institute Young Investigator Award (Institute for Immunity, Transplantation and Infection)
- Society for University Surgeons Resident Scholar award
- NIAID [1U19AI109662, U19AI057229, U54I117925, U01AI089859]
- Bill and Melinda Gates Foundation
Respiratory viral infections are a significant burden to healthcare worldwide. Many whole genome expression profiles have identified different respiratory viral infection signatures, but these have not translated to clinical practice. Here, we performed two integrated, multi-cohort analyses of publicly available transcriptional data of viral infections. First, we identified a common host signature across different respiratory viral infections that could distinguish (1) individuals with viral infections from healthy controls and from those with bacterial infections, and (2) symptomatic from asymptomatic subjects prior to symptom onset in challenge studies. Second, we identified an influenza-specific host response signature that (1) could distinguish influenza-infected samples from those with bacterial and other respiratory viral infections, (2) was a diagnostic and prognostic marker in influenza-pneumonia patients and influenza challenge studies, and (3) was predictive of response to influenza vaccine. Our results have applications in the diagnosis, prognosis, and identification of drug targets in viral infections.
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