RSV Immunoprophylaxis in Infants and Children: Old Standards, New Agents and the Complexities Therein

Bosco A Paes1, Paolo Manzoni2,3, John R Fullarton4

  • 1Hamilton Health Sciences, McMaster University, Hamilton, ON L8N 3Z5, Canada.

Vaccines
|July 27, 2026
PubMed

Insights

New long-acting monoclonal antibodies (mAbs) like nirsevimab and clesrovimab offer single-dose protection against respiratory syncytial virus (RSV) for infants, complementing existing options. These advanced immunoprophylaxis strategies are changing infant immunization programs.

Area of Science:

  • Pediatric Infectious Diseases
  • Immunology
  • Vaccinology

Background:

  • Respiratory syncytial virus (RSV) causes significant lower respiratory tract infections, hospitalizations, and mortality in young children globally.
  • Palivizumab, a monthly monoclonal antibody (mAb), has been the standard for RSV immunoprophylaxis in high-risk infants for 28 years.
  • Recent advancements include long-acting mAbs (nirsevimab, clesrovimab) and a maternal preF vaccine, transforming RSV prevention.

Purpose of the Study:

  • To review and compare the mechanisms of action, pharmacokinetics, efficacy, safety, and cost-effectiveness of nirsevimab and clesrovimab.
  • To use palivizumab as a reference standard for evaluating these newer RSV prevention agents.
  • To assess the impact of these new immunoprophylaxis options on universal infant immunization programs.

Main Methods:

  • Comparative review of nirsevimab and clesrovimab against palivizumab.
  • Analysis of data from clinical trials, considering variations in study populations and endpoint definitions.
  • Evaluation of real-world evidence for nirsevimab and assessment of data gaps for clesrovimab.

Main Results:

  • Nirsevimab and clesrovimab offer single-dose seasonal protection, enabling broader infant populations for immunization compared to palivizumab.
  • All three agents (palivizumab, nirsevimab, clesrovimab) demonstrate broadly comparable protection against severe RSV disease and favorable tolerability profiles.
  • Nirsevimab has growing real-world evidence supporting its effectiveness, while clesrovimab requires further real-world data, especially in high-risk groups.

Conclusions:

  • Nirsevimab and clesrovimab show equivalent efficacy and safety profiles to palivizumab.
  • The choice between these monoclonal antibodies should be guided by cost-effectiveness and local availability.
  • Optimal integration of infant immunoprophylaxis with maternal RSV vaccination programs should be considered.

Related Concept Videos

Respiratory Syncytial Virus Disease01:29

Respiratory Syncytial Virus Disease

Human respiratory syncytial virus (RSV) is a widespread pathogen that primarily targets infants and young children but also poses a serious health risk to elderly and immunocompromised individuals. Belonging to the Pneumoviridae family, RSV is a negative-sense, single-stranded RNA virus within the Pneumovirus genus. Its global health burden is significant, with millions of cases annually resulting in hospitalizations and mortality, particularly in resource-limited settings. Although most...
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
Smallpox01:24

Smallpox

Smallpox is a severe contagious disease caused by the Variola major virus, a double-stranded DNA member of the Poxviridae family.Variola major transmission occurs primarily via inhalation of virus-laden droplets or direct contact with infectious scabs. The incubation period averages approximately seven days, although it may range from 7 to 17 days depending on the inoculum and host factors.Clinically, the prodromal phase is marked by an abrupt onset of high fever, malaise, headache, and myalgia.
Poliomyelitis01:17

Poliomyelitis

Poliomyelitis is caused by poliovirus, a small, non-enveloped, positive-sense RNA virus of the Picornaviridae family and Enterovirus genus. Transmission occurs primarily via the fecal-oral route, often through ingestion of contaminated water or food. The virus initially replicates in the oropharynx and intestinal mucosa, particularly in lymphoid tissues such as the tonsils, Peyer’s patches, and regional lymph nodes. Primary viremia follows, allowing dissemination throughout the body.In most...
Vaccinations01:51

Vaccinations

Overview
Pneumonia IV: Management01:28

Pneumonia IV: Management

The treatment of pneumonia varies based on its severity and the causative pathogen. Here is a structured approach to managing pneumonia, integrating pharmaceutical and supportive care strategies.
Bacterial Pneumonia Treatment
For bacterial pneumonia, antibiotics serve as the cornerstone of therapy. Initial treatment often begins with empirical antibiotics, tailored to the anticipated causative organism and adjusted based on culture results. Key antibiotic choices include: