Modelling the impact of long-acting monoclonal antibody, maternal vaccine and hybrid programs of RSV immunisation in temperate Western Australia
| dc.contributor.author | Giannini, Fiona | en |
| dc.contributor.author | Hogan, Alexandra B. | en |
| dc.contributor.author | Blyth, Christopher C. | en |
| dc.contributor.author | Glass, Kathryn | en |
| dc.contributor.author | Moore, Hannah C. | en |
| dc.date.accessioned | 2026-08-24T07:42:10Z | |
| dc.date.available | 2026-08-24T07:42:10Z | |
| dc.date.issued | 2026-06-20 | en |
| dc.description.abstract | Background: Two RSV immunisations products: a maternal vaccine, Abrysvo, and a long-acting monoclonal antibody, nirsevimab, both designed to prevent RSV illness in infants, have recently become available. Modelling evidence is required to inform how to optimally use these products in immunisation programs to reduce the burden of RSV in young children. Methods: We extend a dynamic transmission model calibrated to RSV-hospitalisation data of children aged <5 years in temperate Western Australia (WA) to simulate a range of potential RSV immunisation programs. Using our model, we estimate the impact of both single-product and hybrid RSV immunisation programs. The analysis considers timing of administration, coverage levels and targeting of high-risk groups. Impact on RSV burden is analysed in the context of the WA setting and the possible significant cost differences between the two products. Results: All programs analysed were effective in reducing RSV burden. Programs using nirsevimab for newborn infants at similar coverage levels to the Abrysvo programs, averted more RSV-hospitalisations annually. Seasonal programs that focused on protection during high RSV activity and programs targeting high-risk infants had the lowest number needed to immunise to avert one RSV-hospitalisation. When dose cost is considered alongside program impact on RSV burden, we find evidence to support further economic analysis of hybrid programs as they could mitigate the cost differential between the two products while remaining highly effective in reducing RSV burden. Conclusions: Our study is the first to comprehensively analyse hybrid RSV immunisation programs that use Abrysvo and nirsevimab. RSV immunisation programs can substantially reduce the burden of RSV in young children. Our modelling analysis provides evidence on immunisation type, timing, coverage, high-risk groups and dosage cost that will support decision makers and can be used in economic evaluations. | en |
| dc.description.sponsorship | This work was partly funded through a Future Health Research and Innovation Fund through the WA Near-miss Awards program and the STAMP RSV Program which is funded through a Stan Perron Charitable Foundation Program Grant ( 00046ProgPart ). ABH is funded by a National Health and Medical Research Council (NHMRC) Investigator Grant and Scientia funding from UNSW. HCM is funded by a Stan Perron Charitable Foundation People Fellowship ( 00018Research P&P ). This work was partly funded through a Future Health Research and Innovation Fund through the WA Near-miss Awards program and the STAMP RSV Program which is funded through a Stan Perron Charitable Foundation Program Grant (00046ProgPart). ABH is funded by a National Health and Medical Research Council (NHMRC) Investigator Grant and Scientia funding from UNSW. HCM is funded by a Stan Perron Charitable Foundation People Fellowship (00018Research P&P). The authors would like to thank the Linkage, Data Outputs and ISPD Client Services Teams at Western Australian Data Linkage Services, as well as the Western Australia Midwife Notification System, Emergency Department Data Collection, Hospital Morbidity Data Collection, Birth and Death Registrations Data Collections, WA Notifiable Infectious Diseases Database, and PathWest Laboratory Medicine Database.The STAMP Investigator Team is Hannah C Moore, Christopher C Blyth, Samantha Carlson, Fiona Giannini, Mohinder Sarna, David Foley, Catherine Hughes, Peter Richmond, Avram Levy, Ewan Cameron. | en |
| dc.description.status | Peer-reviewed | en |
| dc.format.extent | 10 | en |
| dc.identifier.issn | 0264-410X | en |
| dc.identifier.other | PubMed:42176437 | en |
| dc.identifier.other | ORCID:/0000-0001-5905-1310/work/224458426 | en |
| dc.identifier.scopus | 105039763349 | en |
| dc.identifier.uri | https://hdl.handle.net/1885/733814561 | |
| dc.language.iso | en | en |
| dc.rights | Publisher Copyright: © 2026 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0/ | en |
| dc.source | Vaccine | en |
| dc.subject | Abrysvo | en |
| dc.subject | Compartmental model | en |
| dc.subject | Immunisation | en |
| dc.subject | Infant | en |
| dc.subject | Infectious disease modelling | en |
| dc.subject | Maternal vaccine | en |
| dc.subject | Mathematical model | en |
| dc.subject | Nirsevimab | en |
| dc.subject | Respiratory syncytial virus | en |
| dc.subject | RSV | en |
| dc.subject | Transmission model | en |
| dc.title | Modelling the impact of long-acting monoclonal antibody, maternal vaccine and hybrid programs of RSV immunisation in temperate Western Australia | en |
| dc.type | Journal article | en |
| dspace.entity.type | Publication | en |
| local.contributor.affiliation | Giannini, Fiona; Telethon Kids Institute | en |
| local.contributor.affiliation | Hogan, Alexandra B.; Research School of Population Health, National Centre for Epidemiology and Population Health, ANU College of Law, Governance and Policy, The Australian National University | en |
| local.contributor.affiliation | Blyth, Christopher C.; Telethon Kids Institute | en |
| local.contributor.affiliation | Glass, Kathryn; National Centre for Epidemiology and Population Health, Centre of Epidemiology for Policy and Practice, National Centre for Epidemiology and Population Health, ANU College of Law, Governance and Policy, The Australian National University | en |
| local.contributor.affiliation | Moore, Hannah C.; Telethon Kids Institute | en |
| local.identifier.citationvolume | 86 | en |
| local.identifier.doi | 10.1016/j.vaccine.2026.128731 | en |
| local.identifier.pure | 7daf34c7-7b93-4cae-ad58-a92354c73d7f | en |
| local.identifier.url | https://www.scopus.com/pages/publications/105039763349 | en |
| local.type.status | Published | en |