Clinical and immunological aspects of metapneumovirus infection in children
INFECTIOUS DISEASES
Abstract
Introduction.Metapneumovirus infection is one of the leading causes of lower respiratory tract infection in children.The aim of the study—to identify the features of immunopathogenesis and clinical course of metapneumovirus infection in children to predict the severity of the disease and optimize therapeutic approaches.Materials and methods.A retrospective analysis of the medical records of 210 children aged 1 month to 14 years hospitalized in infectious disease hospitals in St. Petersburg from 2019 to 2025 was conducted. Etiological identification was performed using PCR in nasopharyngeal swabs. Cytokine status (IL-1β, -6, -8, -10, -17, IFN-αand -γlevels) was determined using ELISA in serum.Results.Metapneumovirus infection in children was detected in 6.6% of acute respiratory viral infections. Patients with mono-metapneumovirus infection under 3 years of age accounted for 72%, of which 53% had lower respiratory tract lesions. Acute obstructive laryngitis was most often observed in children aged 1–3 years (23.4%). Children with grade I laryngeal stenosis accounted for 64.3%. Acute bronchitis/BOS was more often recorded in children under 1 year (48.8%) and 1-3 years (46.7%). Grade I–II respiratory failure was observed mainly in young patients (85.7%). Pneumonia was diagnosed in 21.5% of children under 1 year of age. Activation of cellular immunity was accompanied by an increase in proinflammatory cytokines (IL-1β, -6, -8, -17) and an anti-inflammatory cytokine (IL-10), which plays a role in limiting excessive inflammation. A simultaneous decrease in interferon levels (IFN-αand -γ) was observed.Conclusions.Metapneumovirus infection in young children primarily affects the lower respiratory tract and is associated with a high rate of complications. The immunopathogenesis of this infection is characterized by increased production of proinflammatory and anti-inflammatory cytokines, coupled with decreased interferon levels, reflecting an imbalance in the immune response that contributes to the severity of clinical manifestations.
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