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Updated: Apr 14, 2026

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
Host response to respiratory syncytial virus infection
Lourdes Arruvito1, Silvina Raiden, Jorge Geffner
1aInstituto de Inmunología, Genética y Metabolismo (INIGEM), UBA-CONICET, Hospital de Clínicas 'José de San Martín' bHospital General de Niños 'Pedro de Elizalde' cInstituto de Investigaciones Biomédicas en Retrovirus y SIDA (INBIRS), UBA-CONICET, Buenos Aires, Argentina.
Insights
Respiratory syncytial virus (RSV) infection poses a significant threat to infants, causing severe illness and death. Understanding the immune response is crucial for developing effective vaccines and treatments against this common respiratory virus.
Area of Science:
- Immunology
- Virology
- Pediatrics
Background:
- Respiratory syncytial virus (RSV) is a major cause of infant bronchiolitis and hospitalization, with no current vaccine.
- Therapeutic options for RSV are limited, primarily supportive care.
- Significant knowledge gaps exist regarding immune mechanisms and risk factors for severe RSV infection.
Purpose of the Study:
- To review recent findings on the immune response to RSV infection.
- To understand the role of innate and adaptive immunity in RSV pathogenesis and resolution.
- To highlight the importance of studying immune responses in young children, the primary risk group.
Main Methods:
- Review of recent studies on RSV immunology.
- Analysis of findings from mouse models and human infant studies.
- Examination of the roles of various immune cells (T cells, innate immune cells) in RSV infection.
Main Results:
- The early innate immune response is critical in RSV bronchiolitis pathogenesis.
- Adaptive immune responses involving TH1, TH2, TH17, regulatory T cells, and CD8 T cells are key to RSV infection.
- Recent research has advanced understanding of immune responses in high-risk young children.
Conclusions:
- A complete understanding of protective and harmful immune responses to RSV in young children is still needed.
- Further research is required to address remaining challenges in RSV immunology.
- Developing effective interventions for RSV necessitates a deeper comprehension of the immune system's role.
Purpose Of Review:
Respiratory syncytial virus (RSV) infection is the leading cause of bronchiolitis and hospitalization in young infants and causes 100, 000-200, 000 deaths annually. There is still no licensed vaccine against RSV infection and the therapeutic options are mainly supportive. Despite almost six decades of research, important knowledge gaps remain with respect to the characterization of immune mechanisms responsible for protection and pathogenesis, as well as to the identification of risk factors that predict the severity of infection.
Recent Findings:
Observations made in mouse models and young children suggest that the early innate immune response plays a major role in the pathogenesis of bronchiolitis due to RSV infection. Recent studies have improved our understanding of the role of the adaptive immune response mediated by TH1, TH2, TH17, regulatory T cells, and CD8 T cells in the pathogenesis and resolution of RSV infection. Moreover, investigations performed in the last years have made important contributions to our knowledge of the immune response in young children, the principal risk group for severe disease.
Summary:
A comprehensive understanding of how the protective and deleterious immune response during the course of RSV infection is induced in young children remains a challenge over the coming years.
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