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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
Disease Severity of Respiratory Syncytial Virus Infection in Hospitalized Children
Costanza Di Chiara1, Vera Rigamonti2, Beatrice Rita Campana3
1Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Insights
Coinfections with rhinovirus or other viruses did not increase the severity of respiratory syncytial virus (RSV) acute respiratory tract infections in hospitalized children. Understanding RSV coinfection impacts disease management and prevention strategies.
Area of Science:
- Pediatrics
- Infectious Diseases
- Virology
Background:
- Respiratory syncytial virus (RSV) is a primary cause of pediatric acute respiratory tract infection (ARTI) hospitalizations.
- The impact of viral coinfections in RSV-related ARTIs on disease severity is debated and requires clarification.
- Evolving RSV prevention strategies necessitate a better understanding of RSV coinfection phenotypes.
Purpose of the Study:
- To investigate the association between RSV monoinfection, RSV-rhinovirus coinfection, and RSV-non-rhinovirus coinfection and disease severity in hospitalized children.
- To evaluate the clinical implications of viral coinfections in the context of RSV prevention.
Main Methods:
- A multicenter retrospective cohort study included 231 children aged ≤5 years hospitalized with laboratory-confirmed RSV infection.
- Patients were categorized into RSV monoinfection, RSV-rhinovirus coinfection, or RSV-non-rhinovirus coinfection groups.
- Severe disease was defined as ICU admission, need for respiratory/hemodynamic support, or death; Poisson regression analysis was used.
Main Results:
- RSV monoinfection occurred in 51.1%, RSV-rhinovirus coinfection in 28.1%, and RSV-non-rhinovirus coinfection in 20.8% of cases.
- Severe disease rates were 80.5% for monoinfection, 70.8% for RSV-rhinovirus, and 75.0% for RSV-non-rhinovirus coinfection.
- Adjusted analyses showed no significant association between RSV-rhinovirus or RSV-non-rhinovirus coinfection and increased disease severity.
Conclusions:
- RSV-rhinovirus and RSV-non-rhinovirus coinfections were not associated with increased disease severity in hospitalized children.
- Findings support pathogen-specific interpretation of multiplex diagnostic results for RSV infections.
- Results inform clinical risk stratification for pediatric ARTI management amid expanding RSV prevention.
Abstract:
Background: Respiratory syncytial virus (RSV) is a leading cause of hospitalization for acute respiratory tract infection (ARTI) in young children. Respiratory viral coinfections are frequently identified in RSV-related ARTIs, yet their impact on disease severity remains controversial and may vary according to the co-pathogen involved. In the context of evolving RSV prevention strategies, a clearer understanding of RSV coinfection phenotypes is needed. Methods: We conducted a multicenter retrospective cohort study of children aged ≤ 5 years hospitalized for ARTI at two Italian tertiary-care pediatric hospitals between 1 September 2022 and 30 April 2025. Children with laboratory-confirmed RSV infection detected by multiplex polymerase chain reaction were included. Patients were classified as having RSV monoinfection, RSV-rhinovirus coinfection, or RSV-non-rhinovirus coinfection. Severe disease was defined as a composite outcome including intensive care unit (ICU) admission, need for respiratory or hemodynamic support, or death. Association between infection status and severe disease was evaluated using a Poisson regression model with robust variance, adjusted for age, sex, and comorbidities. Results: Among 231 RSV-related hospitalizations, 118 (51.1%) were classified as RSV monoinfection, 65 (28.1%) as RSV-rhinovirus coinfection, and 48 (20.8%) as RSV-non-rhinovirus coinfection. Children with RSV-rhinovirus coinfection were older and had shorter hospital stays. Severe disease occurred in 80.5% of RSV monoinfections, 70.8% of RSV-rhinovirus coinfections, and 75.0% of RSV-non-rhinovirus coinfections. After adjustment, neither RSV-rhinovirus coinfection (adjusted risk ratio [aRR]: 0.93; 95% confidence interval [95% CI]: 0.80-1.13) nor RSV-non-rhinovirus coinfection (aRR: 0.99; 95% CI: 0.83-1.18) was associated with increased disease severity compared with RSV monoinfection. Conclusions: RSV-rhinovirus and RSV-non-rhinovirus coinfections were not associated with greater disease severity compared with RSV monoinfection in hospitalized children. These findings support pathogen-specific interpretation of multiplex diagnostic results and inform clinical risk stratification in the era of expanding RSV prevention strategies.
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