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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
The Emerging Landscape of Respiratory Viral Infections in Immunocompromised Children
Paschalis Evangelidis1, Elias Iosifidis2, Athanasios Tragiannidis3
1Second Propedeutic Department of Internal Medicine, Hippokration Hospital, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece.
Insights
Respiratory viral infections (RVIs) pose significant risks for immunocompromised children, especially those with cancer or transplants. Early diagnosis and careful interpretation of viral detection are crucial for effective management and improved outcomes.
Area of Science:
- Pediatric Infectious Diseases
- Immunocompromised Hosts
- Virology
Background:
- Respiratory viral infections (RVIs) are significant complications in immunocompromised children, including those with malignancies and transplant recipients.
- Advances in cancer therapy and diagnostics have increased the population at risk and viral detection rates.
- Differentiating incidental viral detection from clinically significant disease presents a challenge.
Purpose of the Study:
- To review current evidence on the epidemiology, clinical manifestations, diagnostics, and management of RVIs in immunocompromised pediatric populations.
- To highlight the challenges in interpreting viral detection in this vulnerable group.
- To underscore the need for integrating virologic data into pediatric oncology care.
Main Methods:
- Literature review of current evidence.
- Analysis of diagnostic strategies, primarily nucleic acid amplification tests.
- Examination of clinical manifestations and management approaches.
Main Results:
- RVIs in immunocompromised children present with diverse clinical manifestations, ranging from mild to severe disease.
- Diagnostic interpretation is complex due to prolonged viral shedding, co-detection, and overlapping syndromes.
- Viral detection impacts infection control, antimicrobial stewardship, and treatment timing.
Conclusions:
- There is a need for structured, risk-adapted integration of virologic data into pediatric oncology care.
- Improved diagnostic interpretation is essential for managing RVIs in immunocompromised children.
- Effective management strategies are crucial to reduce morbidity and mortality.
Abstract:
Respiratory viral infections (RVIs) have been described traditionally as clinically important infectious complications in pediatric patients with immunosuppression, particularly in those with malignancies (hematological or solid) and recipients of hematopoietic cell or solid organ transplantation. Specifically, advances in the field of cancer therapy and novel immune-based pharmaceuticals have significantly expanded the population of children with prolonged and complex immunosuppression, whereas the widespread use and availability of molecular diagnostics have increased the detection of respiratory viruses. Additionally, these developments have improved the etiologic identification of RVIs, while introducing important challenges in clinical interpretation, mainly in differentiating incidental viral identification from clinically significant diseases. Furthermore, RVIs in immunocompromised children are characterized by heterogeneous and diverse clinical manifestations, with a range from mild upper respiratory tract involvement to severe lower respiratory tract disease, which can lead to substantial morbidity and mortality. Diagnostic strategies in this field are primarily based on nucleic acid amplification tests, requiring careful interpretation because of the possible prolonged viral shedding, co-detection, and overlapping infectious syndromes. Beyond direct clinical consequences, viral detection has an impact on infection control measures, antimicrobial stewardship decisions, and the timing of therapies. In this literature review, we offer an overview of current evidence on the epidemiology, clinical manifestations, diagnostic approaches, and management of RVIs in immunocompromised pediatric populations, underscoring the unmet need for structured, risk-adapted integration of virologic data into pediatric oncology care.
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