Tino F Schwarz, Shinn-Jang Hwang, Pedro Ylisastigui, Chiu-Shong Liu, Kenji Takazawa, Makoto Yono, John E Ervin, Charles P Andrews, Charles Fogarty, Tamara Eckermann, Delphine Collete, Magali de Heusch, Nathalie De Schrevel, Bruno Salaun, Axel Lambert, Céline Maréchal, Aurélie Olivier, Phoebe Nakanwagi, Marc Lievens, Veronica Hulstrøm
The Journal of infectious diseases 2024 Jul 25The recently approved AS01E-adjuvanted respiratory syncytial virus (RSV) prefusion F protein-based vaccine for older adults (RSVPreF3 OA) demonstrated high efficacy against RSV-related disease in ≥60-year-olds. This ongoing phase 3 study in ≥60-year-olds evaluates immune persistence until 3 years after RSVPreF3 OA vaccination. Here, we describe interim results on humoral and cell-mediated immunogenicity, reactogenicity, and safety until 1 year post-dose 1. In total, 1653 participants were vaccinated. One month post-dose 1, neutralization titers increased 10.5-fold (RSV-A) and 7.8-fold (RSV-B) vs pre-dose 1. Titers then declined to levels 4.4-fold (RSV-A) and 3.5-fold (RSV-B) above pre-dose 1 at month 6 and remained 3.1-fold (RSV-A) and 2.3-fold (RSV-B) above pre-dose 1 levels after 1 year. RSVPreF3-binding immunoglobulin G levels and CD4+ T-cell frequencies showed similar kinetics. Solicited administration-site and systemic adverse events (mostly mild to moderate and transient) were reported by 62.2% and 49.5% of participants. Serious adverse events were reported by 3.9% of participants within 6 months post-dose 1; 1 case was considered vaccine related. One RSVPreF3 OA dose elicited cell-mediated and RSV-A- and RSV-B-specific humoral immune responses that declined over time but remained above pre-dose 1 levels for at least 1 year. The vaccine was well tolerated with an acceptable safety profile. Clinical Trials Registration. NCT04732871 (ClinicalTrials.gov). © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.
Tino F Schwarz, Shinn-Jang Hwang, Pedro Ylisastigui, Chiu-Shong Liu, Kenji Takazawa, Makoto Yono, John E Ervin, Charles P Andrews, Charles Fogarty, Tamara Eckermann, Delphine Collete, Magali de Heusch, Nathalie De Schrevel, Bruno Salaun, Axel Lambert, Céline Maréchal, Aurélie Olivier, Phoebe Nakanwagi, Marc Lievens, Veronica Hulstrøm. Immunogenicity and Safety Following 1 Dose of AS01E-Adjuvanted Respiratory Syncytial Virus Prefusion F Protein Vaccine in Older Adults: A Phase 3 Trial. The Journal of infectious diseases. 2024 Jul 25;230(1):e102-e110
PMID: 39052726
View Full Text