Antibody response to respiratory syncytial virus infection in children <18 months old

Susanna Esposito1, Elisa Scarselli2, Mara Lelii1

  • 1a Paediatric Highly Intensive Care Unit , Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico , Milan , Italy.

Insights

Natural respiratory syncytial virus (RSV) infection elicits a weak antibody response in infants younger than 7 months. Vaccines must induce a stronger immune response in early infancy to protect against severe lower respiratory tract infections (LRTIs).

Area of Science:

  • Immunology
  • Pediatrics
  • Virology

Background:

  • Respiratory syncytial virus (RSV) is a major cause of lower respiratory tract infections (LRTIs) in infants.
  • Understanding the natural immune response to RSV is crucial for developing effective vaccines.
  • Younger children are at the highest risk for severe RSV-related illness.

Purpose of the Study:

  • To evaluate the neutralizing antibody response to RSV infection in healthy children under 18 months old.
  • To compare the antibody response and viral shedding in different age groups and disease severities.
  • To inform the development of RSV vaccines for infants.

Main Methods:

  • Prospective cohort study of 89 healthy children <18 months old during an RSV season.
  • Weekly nasopharyngeal swabs for RSV detection via real-time PCR.
  • Blood samples collected to determine geometric mean neutralizing antibody titres (GMT) against RSV.

Main Results:

  • 39.3% of children had RSV detected; older children (≥7 months) showed a significantly higher antibody response.
  • A ≥4-fold increase in GMT was associated with older age and LRTIs.
  • Longer viral shedding was observed in older children, those with higher viral loads, and those with LRTIs, but not associated with immune response.

Conclusions:

  • Natural RSV infection induces a limited immune response in younger infants.
  • RSV vaccines need to elicit a more robust immune response than natural infection, especially in the first months of life.
  • This is critical for protecting vulnerable infants from severe LRTIs.