Transcriptomic response and immunological responses to chimpanzee adenovirus- and MVA viral-vectored vaccines for RSV in healthy adults

Author:

Green C12,McGinley J1ORCID,Sande C1,Capone S3,Makvandi-Nejad S4,Vitelli A3,Silva-Reyes L1,Bibi S1,Otasowie C1,Sheerin D1,Thompson A1,Dold C1,Klenerman P5,Barnes E5,Dorrell L4,Rollier C1,Pollard A1,O’Connor D1

Affiliation:

1. Oxford Vaccine Group, Department of Paediatrics and the NIHR Oxford Biomedical Research Centre, University of Oxford , Oxford , UK

2. Institute of Microbiology & Infection, University of Birmingham , Birmingham , UK

3. Experimental Vaccinology Department, ReiThera Srl , Roma , Italy

4. Nuffield Department of Medicine, University of Oxford NDM Research Building , Oxford , UK

5. Experimental Medicine Division, Nuffield Department of Medicine, University of Oxford , Oxford , UK

Abstract

AbstractCohorts of healthy younger adults (18–50yrs) and healthy older adults (60–75yrs) were immunized intramuscularly or intranasally with an adenovirus-vectored RSV vaccine (PanAd3-RSV) as a prime dose and boosted with PanAd3-RSV or a poxvirus-vectored vaccine (MVA-RSV) encoding the same insert. Whole blood gene expression was measured at baseline, 3- and 7-days post vaccination. Intramuscular prime vaccination with PanAd3-RSV induced differential expression of 643 genes (DEGs, FDR < 0.05). Intranasal prime vaccination with PanAd3-RSV did not induce any differentially expressed genes (DEGs) in blood samples at 3 days post vaccination. Intranasally primed participants showed greater numbers of DEGS on boosting than intramuscularly primed participants. The most highly enriched biological processes related to DEGs after both prime and boost vaccination were type-1 interferon related pathways, lymphocytic and humoral immune responses.

Funder

Wellcome Trust

NIHR Oxford Biomedical Research Centre

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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