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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
Pulmonary surfactant in respiratory syncytial virus bronchiolitis: the role in pathogenesis and clinical implications
Eliane Roseli Barreira1, Alexander Roberto Precioso, Albert Bousso
1University Hospital, University of Sao Paulo, Sao Paulo, Brazil. eliane@hu.usp.br.
Insights
Respiratory syncytial virus (RSV) bronchiolitis impacts infant health, potentially leading to asthma. Changes in pulmonary surfactant, including SP-A and SP-D, may worsen RSV disease, suggesting surfactant replacement as a novel therapy.
Area of Science:
- Pulmonology
- Virology
- Immunology
Background:
- Respiratory syncytial virus (RSV) bronchiolitis is a major cause of infant hospitalization and linked to childhood asthma.
- Current treatments for severe RSV bronchiolitis are limited to supportive care and mechanical ventilation.
- Pulmonary surfactant, crucial for lung function, and its proteins SP-A and SP-D, integral to innate immunity, are implicated in RSV pathogenesis.
Purpose of the Study:
- To review the literature on pulmonary surfactant alterations in severe RSV bronchiolitis.
- To analyze the relationship between surfactant changes, inflammation, and immune response in RSV.
- To explore the potential of pulmonary surfactant replacement therapy for RSV bronchiolitis.
Main Methods:
- Literature review and analysis of existing evidence.
- Examination of the role of surfactant proteins SP-A and SP-D in viral clearance and inflammation.
- Assessment of studies investigating pulmonary surfactant composition changes in RSV patients.
Main Results:
- Severe RSV bronchiolitis is associated with significant changes in pulmonary surfactant content and composition.
- Deficiencies in surfactant proteins SP-A and SP-D may impair viral clearance and exacerbate inflammation.
- Evidence suggests a link between altered surfactant and the severity of RSV-induced lung disease.
Conclusions:
- Pulmonary surfactant plays a critical role in the pathogenesis of severe RSV bronchiolitis.
- Understanding surfactant's role in immunity and inflammation could lead to new therapeutic strategies.
- Pulmonary surfactant replacement therapy presents a potential novel treatment approach for severe RSV bronchiolitis.
Abstract:
Respiratory syncytial virus (RSV) bronchiolitis is the leading cause of lower respiratory tract infection, and the most frequent reason for hospitalization among infants throughout the world. In addition to the acute consequences of the disease, RSV bronchiolitis in early childhood is related to further development of recurrent wheezing and asthma. Despite the medical and economic burden of the disease, therapeutic options are limited to supportive measures, and mechanical ventilation in severe cases. Growing evidence suggests an important role of changes in pulmonary surfactant content and composition in the pathogenesis of severe RSV bronchiolitis. Besides the well-known importance of pulmonary surfactant in maintenance of pulmonary homeostasis and lung mechanics, the surfactant proteins SP-A and SP-D are essential components of the pulmonary innate immune system. Deficiencies of such proteins, which develop in severe RSV bronchiolitis, may be related to impairment in viral clearance, and exacerbated inflammatory response. A comprehensive understanding of the role of the pulmonary surfactant in the pathogenesis of the disease may help the development of new treatment strategies. We conducted a review of the literature to analyze the evidences of pulmonary surfactant changes in the pathogenesis of severe RSV bronchiolitis, its relation to the inflammatory and immune response, and the possible role of pulmonary surfactant replacement in the treatment of the disease.
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