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An In vitro Model to Study Immune Responses of Human Peripheral Blood Mononuclear Cells to Human Respiratory Syncytial Virus Infection
Published on: December 10, 2013
Airway Gene Expression Correlates of Respiratory Syncytial Virus Disease Severity and Microbiome Composition in
Chin-Yi Chu1,2, Xing Qiu3, Matthew N McCall3
1Division of Neonatology and Pediatric Molecular and Personalized Medicine Program, University of Rochester Medical Center, Rochester, New York, USA.
Insights
Respiratory syncytial virus (RSV) causes severe infant respiratory illness. Gene expression patterns and airway microbes in infants with RSV infection reveal distinct signatures for severe versus mild/moderate disease.
Area of Science:
- Pediatric infectious diseases
- Molecular biology
- Immunology
Background:
- Respiratory syncytial virus (RSV) is a primary cause of severe respiratory illness in infants.
- The underlying factors contributing to severe RSV illness in most infants remain unclear.
Purpose of the Study:
- To investigate airway gene expression and microbiota in infants with RSV infection.
- To identify molecular signatures and microbial associations linked to RSV disease severity.
Main Methods:
- Recruited a cohort of 106 infants with primary RSV infection.
- Assayed airway gene expression and microbiota composition.
- Employed rigorous statistical methods to correlate molecular and microbial data with disease severity.
Main Results:
- Identified an airway gene expression signature of severe RSV illness characterized by excessive chemokine expression.
- Found an association between Haemophilus influenzae, disease severity, and airway lymphocyte accumulation.
- Observed absent acute interferon signaling in severe RSV cases, unlike mild/moderate cases.
Conclusions:
- Airway gene expression patterns effectively differentiate between mild/moderate and severe RSV illness in infants.
- Identified potential biomarkers for therapeutic targets and for measuring intervention efficacy in RSV infections.
Background:
Respiratory syncytial virus (RSV) is the leading cause of severe respiratory disease in infants. The causes and correlates of severe illness in the majority of infants are poorly defined.
Methods:
We recruited a cohort of RSV-infected infants and simultaneously assayed the molecular status of their airways and the presence of airway microbiota. We used rigorous statistical approaches to identify gene expression patterns associated with disease severity and microbiota composition, separately and in combination.
Results:
We measured comprehensive airway gene expression patterns in 106 infants with primary RSV infection. We identified an airway gene expression signature of severe illness dominated by excessive chemokine expression. We also found an association between Haemophilus influenzae, disease severity, and airway lymphocyte accumulation. Exploring the time of onset of clinical symptoms revealed acute activation of interferon signaling following RSV infection in infants with mild or moderate illness, which was absent in subjects with severe illness.
Conclusions:
Our data reveal that airway gene expression patterns distinguish mild/moderate from severe illness. Furthermore, our data identify biomarkers that may be therapeutic targets or useful for measuring efficacy of intervention responses.
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