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Abstract

The development of an effective vaccine against respiratory syncytial virus (RSV) has been hampered by major difficulties that occurred in the 1960s when a formalin-inactivated vaccine led to increased severity of RSV disease after acquisition of the virus in the RSV season after vaccination. Recent renewed efforts to develop a vaccine have resulted in about 38 candidate vaccines and monoclonal antibodies now in clinical development. The target populations for effective vaccination are varied and include neonates, young children, pregnant women, and older adults. The reasons for susceptibility to infection in each of these groups may be different and, therefore, could require different vaccine types for induction of protective immune responses, adding a further challenge for vaccine development. Here, we review the current knowledge of RSV vaccine development for these target populations and propose a view and rationale for prioritizing RSV vaccine development.
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Science Translational Medicine
Volume 12 | Issue 535
March 2020

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Received: 7 March 2019
Accepted: 25 September 2019

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Acknowledgments

Funding: We were supported by the NIHR Oxford Biomedical Research Centre. S.B.D., A.J.P., and C.J.S. are members of the REspiratory Syncytial virus Consortium in Europe (RESCEU). RESCEU has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement no. 116019. This Joint Undertaking received support from the European Union’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). C.J.S. is supported by fellowship funding from the Wellcome Trust (WT105882MA). Competing interests: A.J.P. chairs the UK Department of Health and Social Care’s Joint Committee on Vaccination and Immunisation (JCVI) and the European Medicines Agency Scientific Advisory Group on Vaccines and is a member of the World Health Organization’s Strategic Group of Experts. The views expressed in this manuscript do not necessarily reflect the views of these agencies. A.J.P. and C.S.R. are Jenner Institute investigators. S.B.D. has been an investigator on studies funded by Janssen and MedImmune; all funds have been paid to S.B.D.’s institution, and S.B.D. has received no personal payments. The other authors declare that they have no competing interests.

Authors

Affiliations

Oxford Vaccine Group, Department of Paediatrics and the NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LE, UK.
Institute of Infection and Immunity, St George’s, University of London, London SW17 0RE, UK.
Rachael S. Barr
Taunton and Somerset NHS Foundation Trust, Taunton TA1 5DA, UK.
Oxford Vaccine Group, Department of Paediatrics and the NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LE, UK.
Christopher A. Green
Oxford Vaccine Group, Department of Paediatrics and the NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LE, UK.
Oxford Vaccine Group, Department of Paediatrics and the NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LE, UK.
Oxford University Hospitals NHS Foundation Trust, Oxford OX3 9DU, UK.
Oxford Vaccine Group, Department of Paediatrics and the NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LE, UK.
KEMRI-Wellcome Trust Research Programme, Kilifi 80108, Kenya.

Funding Information

NIHR Oxford Biomedical Research Centre

Notes

*Corresponding author. Email: [email protected] (S.B.D.); [email protected] (C.J.S.)

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