npj Vaccines
(Apr 2025)
Risk analysis for outpatient experimental infection as a pathway for affordable RSV vaccine development
E. Z. Siegal,
J. M. H. Schoevers,
J. Terstappen,
E. M. Delemarre,
S. L. Johnston,
L. F. van Beek,
D. Bogaert,
C. Chiu,
D. A. Diavatopoulos,
D. M. Ferreira,
S. B. Gordon,
F. G. Hayden,
M. I. de Jonge,
M. B. B. McCall,
H. I. McShane,
A. M. Minassian,
P. J. M. Openshaw,
A. J. Pollard,
J. Sattabongkot,
R. C. Read,
A. Troelstra,
M. C. Viveen,
A. Wilder-Smith,
M. van Wijk,
L. J. Bont,
N. I. Mazur
Affiliations
E. Z. Siegal
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
J. M. H. Schoevers
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
J. Terstappen
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
E. M. Delemarre
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
S. L. Johnston
Virtus Respiratory Research Ltd
L. F. van Beek
Laboratory of Medical Immunology, Radboud University Medical Center
D. Bogaert
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
C. Chiu
Virtus Respiratory Research Ltd
D. A. Diavatopoulos
Laboratory of Medical Immunology, Radboud University Medical Center
D. M. Ferreira
Oxford Vaccine Group, Department of Paediatrics, The NIHR Oxford Biomedical Research Centre, University of Oxford
S. B. Gordon
Department of Clinical Sciences, Liverpool School of Tropical Medicine
F. G. Hayden
Division of infectious Diseases and International Health, University of Virginia, School of Medicine
M. I. de Jonge
Laboratory of Medical Immunology, Radboud University Medical Center
M. B. B. McCall
Radboud Center for Infectious Diseases, Radboud university medical Center
H. I. McShane
Oxford Vaccine Group, Department of Paediatrics, The NIHR Oxford Biomedical Research Centre, University of Oxford
A. M. Minassian
Oxford Vaccine Group, Department of Paediatrics, The NIHR Oxford Biomedical Research Centre, University of Oxford
P. J. M. Openshaw
National Heart and Lung Institute, Imperial College London
A. J. Pollard
Oxford Vaccine Group, Department of Paediatrics, The NIHR Oxford Biomedical Research Centre, University of Oxford
J. Sattabongkot
Mahidol Vivax Research Unit, Faculty of Tropical Medicine, Mahidol University
R. C. Read
Faculty of Medicine and Institute for Life Sciences, University of Southampton
A. Troelstra
Medical Microbiology, University Medical Center Utrecht
M. C. Viveen
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
A. Wilder-Smith
Heidelberg Institute of Global Health, University of Heidelberg
M. van Wijk
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
L. J. Bont
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
N. I. Mazur
Department of Pediatric Infectious Diseases and Immunology, Wilhelmina Children’s Hospital, University Medical Center Utrecht
DOI
https://doi.org/10.1038/s41541-025-01125-w
Journal volume & issue
Vol. 10,
no. 1
pp.
1
– 9
Abstract
Read online
Abstract Controlled human infection models (CHIMs) are an important tool for accelerating clinical development of vaccines. CHIM costs are driven by quarantine facilities but may be reduced by performing CHIM in the outpatient setting. Furthermore, outpatient CHIMs offer benefits beyond costs, such as a participant-friendly approach and increased real-world aspect. We analyze safety, logistic and ethical risks of respiratory syncytial virus (RSV) CHIM in the outpatient setting. A review of the literature identified outpatient CHIMs involving respiratory pathogens. RSV transmission risk was assessed using data from our inpatient and outpatient RSV CHIMs (EudraCT 020-004137-21). Fifty-nine outpatient CHIMs using RSV, Streptococcus pneumoniae, rhinovirus, and an ongoing Bordetella Pertussis outpatient CHIM were included. One transmission event was recorded. In an inpatient RSV CHIM, standard droplet and isolation measures were sufficient to limit RSV transmission and no symptomatic third-party transmission was measured in the first outpatient RSV CHIM. Logistic and ethical advantages support outpatient CHIM adoption. We propose a framework for outpatient RSV CHIM with risk mitigation strategies to enhance affordable vaccine development.
Published in npj Vaccines
ISSN
2059-0105 (Online)
Publisher
Nature Portfolio
Country of publisher
United Kingdom
LCC subjects
Medicine: Internal medicine: Specialties of internal medicine: Immunologic diseases. Allergy
Medicine: Internal medicine: Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Website
https://www.nature.com/npjvaccines/
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