RSV Vaccines: Available Types and Comparability
There are currently three RSV vaccines approved for older adults, and mRESVIA (mRNA-1345) is comparable to RSVPreF3 (Arexvy) in terms of target population and indication, though they use different vaccine technologies. 1
Available RSV Vaccine Types
The three approved RSV vaccines for older adults are:
- RSVPreF3 (Arexvy): A recombinant RSV pre-fusion F protein adjuvanted with AS01E, approved for adults ≥50 years 1
- RSVpreF (Abrysvo): A recombinant bivalent RSV-A and RSV-B pre-fusion F protein (non-adjuvanted), approved for adults ≥60 years 1
- mRESVIA (mRNA-1345): An mRNA-based vaccine, approved for adults ≥60 years 1
Key Differences Between Vaccine Technologies
RSVPreF3 (Arexvy) Characteristics
- Contains AS01E adjuvant, which enhances immune response 2
- Demonstrated 82.6% efficacy against RSV-associated lower respiratory tract disease in the first season 2
- Showed 94.1% efficacy against severe RSV-related lower respiratory tract disease 2
- Maintains efficacy for at least three RSV seasons, though efficacy decreases over time 3
- Cumulative efficacy over three seasons was 62.9% against RSV-LRTD 3
- Only vaccine approved for adults aged 50-59 years with risk factors 4
RSVpreF (Abrysvo) Characteristics
- Non-adjuvanted bivalent formulation 5
- Demonstrated 88.9% efficacy against RSV-associated LRTI with ≥3 symptoms at end of season 1 5
- Showed 77.8% efficacy at end of season 2 5
- Maintains efficacy for at least two RSV seasons 4
- Also approved for maternal immunization during pregnancy (32-36 weeks) 6
mRESVIA (mRNA-1345) Characteristics
- Uses mRNA technology platform 1
- Approved for adults ≥60 years 1
- Limited comparative data available in the provided evidence
Comparability Assessment
mRESVIA and RSVPreF3 are comparable in their approved age indication for adults ≥60 years, but RSVPreF3 has the unique advantage of approval down to age 50 years for high-risk individuals. 1 Both vaccines target the same RSV prefusion F protein antigen, though they use different delivery mechanisms (mRNA versus recombinant protein with adjuvant). 1
Important Clinical Considerations
- All three vaccines are considered interchangeable for adults ≥60 years based on guideline recommendations that do not express preference among available vaccines 4
- For adults aged 50-59 years with risk factors, RSVPreF3 is the only approved option 4, 1
- Both RSVPreF3 and RSVpreF demonstrate high effectiveness (75-82%) against RSV-associated hospitalization in real-world post-licensure studies 4
- The Portuguese guideline explicitly states that "two RSV vaccines are currently available in Portugal" (referring to RSVPreF3 and RSVpreF), suggesting mRESVIA may have more limited availability in some regions 4
Safety Profile Comparison
- Both RSVPreF3 and RSVpreF are generally well tolerated with acceptable safety profiles 4
- Most adverse events are transient and mild-to-moderate in severity 4, 2
- RSVPreF3 is more reactogenic than placebo, with injection-site pain and fatigue being most common 4
- Serious adverse event rates are similar between vaccine and placebo groups for both RSVPreF3 (4.4% vs 4.3%) and RSVpreF (4.3% vs 4.1%) 4
- Post-licensure surveillance has identified potential increased risk for Guillain-Barré syndrome after protein subunit RSV vaccination 1
Practical Pitfalls to Avoid
- Do not assume all three vaccines have identical age indications - only RSVPreF3 is approved for the 50-59 year age group 1
- Do not require extensive documentation of risk factors - patient attestation is sufficient to avoid barriers to vaccination 1
- Be aware that co-administration with influenza vaccines may result in numerically lower antibody titers for both RSV and influenza, though clinical significance is unknown 4, 7