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Respiratory syncytial virus (RSV) is a leading cause of severe lower respiratory tract infection in young children, and a substantial proportion of severe cases occur in previously healthy infants. The gut-lung axis suggests that gut microbiome composition may modulate respiratory immune responses. This prospective observational study in Vietnam will compare gut microbiome profiles and systemic immune cytokine responses between infants with severe RSV infection and those with mild RSV infection, aiming to identify microbiome-immune signatures associated with disease severity.
This is a single-center, prospective observational study conducted at Vietnam National Children's Hospital in Hanoi over 48 months. Approximately 250 infants aged 1-24 months with RT-PCR-confirmed RSV lower respiratory tract infection will be enrolled and classified into severe vs mild groups based on need for advanced respiratory support (HFNC/CPAP/invasive ventilation) and/or PICU admission versus no/low-flow oxygen requirement. Stool samples collected within the first 24 hours of admission will undergo 16S rRNA sequencing (V3-V4 region) to characterize gut microbiome diversity and taxa abundance. Blood samples collected within the first 24 hours will be used to quantify key cytokines (e.g., TNF-α, IL-6, IL-8, IL-1β, IFN-γ, IL-10, IL-17A, IL-22) using ELISA; immune cell subsets may be assessed by flow cytometry. Clinical severity will be assessed using standardized pediatric scores (PRISM III, PELOD, pSOFA) and treatment outcomes will be recorded. The study will evaluate associations among microbiome features, immune response markers, and RSV severity to propose candidate integrated biomarkers for early risk stratification.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Severe RSV group: infants requiring HFNC/CPAP/invasive ventilation and/or PICU admission | Mild RSV group: infants requiring no respiratory support or low-flow oxygen ≤2 L/min via nasal cannula |
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| Measure | Description | Time Frame |
|---|---|---|
| Association between gut microbiome diversity/composition and RSV severity | Differences in gut microbiome diversity and taxonomic composition assessed by 16S rRNA sequencing (alpha diversity, beta diversity, and differential taxa abundance) between severe and mild RSV groups | Within 24 hours of hospital admission |
| Measure | Description | Time Frame |
|---|---|---|
| Systemic cytokine response in severe versus mild RSV infection | Serum concentrations of inflammatory and regulatory cytokines (TNF-α, IL-6, IL-8, IL-1β, IFN-γ, IL-10, IL-17A, IL-22) measured by ELISA All cytokines will be measured using the same assay platform and reported in the same unit of concentration. Unit of measurement is pg/ml | Within 24 hours of hospital admission |
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Inclusion Criteria:
Age 1 to 24 months RT-PCR positive for RSV from respiratory specimen Symptoms consistent with acute lower respiratory tract infection Parent/legal guardian provides informed consent
Exclusion Criteria:
Prematurity <32 weeks gestation or birthweight <1500 g Chronic conditions (e.g., congenital heart disease, chronic lung disease, chronic liver/kidney disease) Primary or acquired immunodeficiency Severe malnutrition (weight-for-age Z-score < -3 SD) Antibiotic use within 2 weeks before admission Probiotic use within 4 weeks before admission Co-infection with other pathogens (viral/bacterial) Stool sample not obtained within 24 hours of admission
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Infants with acute lower respiratory tract infection and RT-PCR-confirmed RSV presenting to Vietnam National Children's Hospital
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Phuc H Phan, M.D. | Contact | +84912880105 | phucph@nch.gov.vn |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Vietnam National Children's Hospital | Hanoi | Vietnam |
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Jan 28, 2026 | Feb 11, 2026 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D018357 | Respiratory Syncytial Virus Infections |
| D001988 | Bronchiolitis |
| ID | Term |
|---|---|
| D018186 | Pneumovirus Infections |
| D018184 | Paramyxoviridae Infections |
| D018701 | Mononegavirales Infections |
| D012327 | RNA Virus Infections |
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Stool microbiome DNA + serum/plasma for cytokines
| Clinical severity scores in RSV infection measured by Pediatric Sequential Organ Failure Assessment (pSOFA) Score | Clinical severity scores in RSV infection measured by Organ dysfunction severity assessed using the Pediatric Sequential Organ Failure Assessment (pSOFA) score (range: 0-24), with higher scores indicating more severe organ dysfunction | within 24 h of hospitalization |
| Integrated microbiome-immune signature predicting severe RSV | Multivariable model performance (AUC/ROC; or adjusted odds ratios for selected taxa + cytokines) | Baseline (first 24h) predicting severity classification during index hospitalization |
| ICU resource utilization | ICU-free days: calculated as 28 minus ICU length of stay for patients discharged alive before Day 28; assigned 0 for patients who die before Day 28 or remain in ICU on/after Day 28. Ventilator-free days: calculated as 28 minus days of invasive mechanical ventilation for patients alive and ventilated <28 days; assigned 0 for patients who die before Day 28 or remain ventilated on/after Day 28. Vasopressor-free days: calculated as 28 minus days receiving vasoactive agents for patients alive and requiring vasoactives <28 days; assigned 0 for patients who die before Day 28 or remain on vasoactives on/after Day 28. Discontinuation requires ≥12 hours without vasoactive support | Up to day 28 |
| D014777 | Virus Diseases |
| D007239 | Infections |
| D001991 | Bronchitis |
| D012141 | Respiratory Tract Infections |
| D001982 | Bronchial Diseases |
| D012140 | Respiratory Tract Diseases |
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |