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Respiratory Syncytial Virus (RSV)

GMJ News knowledge hub · last reviewed August 2026 · Georgian Medical Journal

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Respiratory syncytial virus (RSV) is the leading cause of acute lower respiratory infection in infants globally — causing an estimated 3.6 million hospitalisations and 100,000 child deaths under 5 every year, the vast majority in LMICs (WHO). RSV also causes severe disease in older adults and immunocompromised individuals. The RSV prevention landscape has been transformed by three landmark approvals in 2023-2024: nirsevimab (Beyfortus — monoclonal antibody for all infants), and two vaccines (abrysvo, mResvia) for older adults — representing the most significant advance in RSV prevention in the 60 years since the virus was first isolated.

Key messages

100,000 child deaths/year
RSV causes approximately 100,000 deaths in children under 5 per year — predominantly in LMICs where access to supportive care is limited. RSV is the leading infectious cause of infant hospitalisation globally (WHO).
Revolutionary 2023-2024 prevention
Three landmark approvals have transformed RSV prevention: nirsevimab (Beyfortus — long-acting monoclonal antibody for all infants, 77% efficacy against hospitalisation); abrysvo (maternal vaccine); and mResvia (mRNA vaccine for older adults).
All infants and older adults at risk
RSV causes severe disease at the extremes of age: infants (bronchiolitis — inflammation of small airways) and older adults ≥60 and immunocompromised individuals (pneumonia, respiratory failure). Previously healthy adults rarely develop severe disease.
No specific antiviral treatment
RSV treatment is supportive — oxygen, hydration, and in severe cases mechanical ventilation. Ribavirin has minimal evidence and is rarely used. Prevention through nirsevimab and maternal vaccination is therefore the primary strategy.
Seasonal pattern
RSV follows strong seasonal patterns: in temperate zones, RSV season is autumn to spring (October-March in the Northern Hemisphere). In tropical/subtropical settings, circulation may be more prolonged. Seasonal patterns guide prophylaxis timing.
GAVI and access
Nirsevimab at $100+ per dose is unaffordable for most LMICs. GAVI has committed to including RSV prevention in its portfolio, but access timelines remain uncertain. WHO is prioritising RSV on its immunisation agenda.

Key statistics

3.6M
RSV hospitalisations/year in under 5s
WHO
100K
RSV deaths in under 5s/year
WHO
#1
cause of infant hospitalisation globally
Lancet/WHO
77%
efficacy of nirsevimab vs hospitalisation
MELODY trial
60+ years
since RSV was first isolated (1956)
History
2023
year of landmark nirsevimab and RSV vaccine approvals
FDA/EMA

RSV hospitalisations in children <5 by region — WHO/Lancet 2023

Source: WHO/Lancet Global Burden of RSV. South Asia and Sub-Saharan Africa carry the majority of the severe disease burden.

Glossary of key terms

RSV (Respiratory Syncytial Virus)
WHO
A negative-sense RNA paramyxovirus — the most common cause of bronchiolitis and viral pneumonia in infants globally. Two subtypes (A and B) circulate simultaneously. No natural long-lasting immunity — people can be reinfected throughout life.
Bronchiolitis
WHO/AAP
Inflammation of the small airways (bronchioles) — the most common severe RSV presentation in infants. Causes wheeze, tachypnoea, intercostal recession and difficulty feeding. Managed with oxygen; recovery typically 7-14 days. Hospitalisation required when O2 <92% or feeding compromised.
Nirsevimab (Beyfortus)
FDA/EMA 2023
A long-acting monoclonal antibody (LAMA) targeting RSV prefusion F protein — given as a single IM injection to all infants before or during their first RSV season. 77% efficacy against hospitalisation. A major advance over palivizumab (limited to high-risk infants).
Palivizumab
FDA/WHO
The first RSV prevention monoclonal antibody — available since 1998 for high-risk infants (premature, congenital heart disease, chronic lung disease). Monthly IM injections during RSV season. Superseded by nirsevimab for broader infant use.
Maternal RSV vaccine (abrysvo)
FDA/EMA 2023
A prefusion F subunit RSV vaccine given to pregnant women (32-36 weeks) — generating maternal antibodies that cross the placenta, protecting newborns from birth. 70% efficacy against RSV lower respiratory tract illness. First licensed maternal vaccine for RSV.
mRNA RSV vaccine (mResvia)
FDA 2024
The first mRNA vaccine for RSV — approved for adults aged 60+ (2024). Targets RSV prefusion F protein. Part of the broader mRNA vaccine platform application following COVID-19 success.

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