“What combination vaccines would make sense from a public perspective?” asked Prof. Nohynek. Based on the seasonality of respiratory diseases, combinations of COVID-19, influenza, and RSV vaccines could be administered before the onset of the infectious winter season. Multiple platforms are being assessed, including mRNA (all three viruses), protein subunit, viral vector, inactivated/live virus, and nasal/mucosal vaccines [1].
Combination vaccines are at different stages of development. Positive phase 3 results have been observed with the mRNA-1083 platform, which demonstrated non-inferiority or superiority compared to licensed influenza and COVID-19 vaccines [2]. Other combination vaccines are still in development, but none have yet reported positive phase 3 outcomes [1].
One challenge is the regulatory landscape, with recent, stricter FDA approval requirements further complicating the development process. Additional considerations include regional variation in circulating respiratory viruses, as well as issues of market access and pricing. The Strategic Advisory Group of Experts (SAGE) on Immunisation at the WHO is scheduled to meet at the end of September 2025, with a position paper on priority vaccines and policy recommendations [1].
“Combination vaccines against respiratory viruses are needed to advance national immunisation programme development”, concluded Prof. Nohynek. “Promising candidates are in the clinical pipeline, and the WHO and GAVI, the Vaccine Alliance, have launched a consultation on combination vaccines. To move forward, we need a paradigm shift in regulatory, policy, and financing approaches.”
- Nohynek HM. Synergy in immunisation: The future of combination vaccines against respiratory viruses. 6th ESCMID Vaccines, 10–13 September 2025, Lisbon, Portugal.
- Spergel ARK, et al. JAMA. 2025;333;(22):1977-1987.
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Table of Contents: ESCMID Vaccines 2025
Featured articles
Real-world data confirm PCV20 effectiveness against pneumococcal disease in adults aged ≥65 years
Pneumococcal Vaccination
A quarter of US children have incomplete pneumococcal vaccination by age 2
V116 shows promise for adults at risk of pneumococcal disease
Real-world data confirm PCV20 effectiveness against pneumococcal disease in adults aged ≥65 years
The V116 pneumococcal vaccine is a new option in children at risk for pneumococcal disease
Influenza and COVID-19 Vaccination
Omicron XBB.1.5 vaccination provides effective, but rapidly waning protection in immunocompromised individuals
Intranasal COVID-19 vaccine shows promising results in preclinical mouse models
Influenza vaccine in children shows moderate, broad protection during the 2024-2025 season
Lower age is linked to reduced uptake of influenza and COVID-19 vaccination
RSV vaccination and Immunisation
Combination respiratory vaccines show promise but face key challenges
Adjuvanted RSVPreF3 demonstrates high real-world effectiveness in the USA
RSV immunisation: Maternal versus direct infant immunisation
European pregnant women show openness to maternal RSV vaccination
Infants immunised with nirsevimab have a lower risk of respiratory-related recurrent hospitalisation
Adjuvanted RSVPreF3 can be co-administered with a COVID-19 mRNA vaccine in adults aged ≥50 years
Other Childhood and Routine Vaccinations
Pertussis vaccination: Could an intranasal vaccine help curb the rising cases of whooping cough?
Does the 2+1 vaccination schedule for Haemophilus influenzae type b increase case numbers?
Wastewater poliovirus detections in Europe may reflect seasonal infection patterns rather than consistent importation
Emerging and Future Vaccines
Where do we stand with vaccination for haemolytic streptococci?
The future looks promising for tuberculosis vaccination
Where do alternative vaccine administration routes fit in the clinical landscape?
Malaria immunisation beyond subunit vaccines: Current progress
SARI Definitions and Vaccine Effectiveness
Case definition discrepancies influence VE outcomes
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