Safety, tolerability and viral kinetics during SARS-CoV-2 human challenge

Author:

Killingley Ben1,Mann Alex2ORCID,Kalinova Mariya2,Boyers Alison2,Goonawardane Niluka3,Zhou Jie3,Lindsell Kate4,Hare Samanjit S.5,Brown Jonathan3ORCID,Frise Rebecca3,Smith Emma6,Hopkins Claire7,Noulin Nicolas2,Londt Brandon2,Wilkinson Tom8,Harden Stephen9,McShane Helen10ORCID,Baillet Mark11,Gilbert Anthony4,Jacobs Michael12,Charman Christine4,Mande Priya4,Nguyen-Van-Tam Jonathan S.13,Semple Malcolm G.14ORCID,Read Robert C.8ORCID,Ferguson Neil M.15ORCID,Openshaw Peter J.6ORCID,Rapeport Garth6,Barclay Wendy S.3ORCID,Catchpole Andrew P.2,Chiu Christopher16ORCID

Affiliation:

1. Department of Infectious Diseases, University College London Hospital, London, UK

2. hVIVO Services Ltd., London, UK

3. Department of Infectious Disease, Imperial College London, London, UK

4. UK Vaccine Taskforce, Department of Business, Energy and Industrial Strategy, London, UK

5. Department of Radiology, Royal Free London NHS Foundation Trust, London, UK

6. National Heart and Lung Institute, Imperial College London, London, UK

7. ENT Department, Guy’s and St Thomas’ NHS Foundation Trust, London, UK

8. Faculty of Medicine and Institute for Life Sciences, University of Southampton, and NIHR Southampton Biomedical Research Centre, University Hospital Southampton, Southampton, UK

9. Department of Radiology, Southampton General Hospital, Southampton, UK

10. Department of Paediatrics, University of Oxford, Oxford, UK

11. S-cubed Biometrics, Abingdon, UK

12. Department of Infectious Diseases, Royal Free London NHS Foundation Trust, London, UK

13. Division of Epidemiology and Public Health, University of Nottingham School of Medicine, Nottingham, UK

14. Health Protection Research Unit in Emerging and Zoonotic Infections, Institute of Infection, Veterinary and Ecological Sciences, Faculty of Health and Life Sciences, University of Liverpool, Liverpool; Respiratory Department, Alder Hey Children’s Hospital, Liverpool, UK

15. MRC Centre for Global Infectious Disease Analysis, School of Public Health, Imperial College London, London, UK

16. Imperial College London

Abstract

Abstract To establish a novel SARS-CoV-2 human challenge model, 36 volunteers aged 18-29 years without evidence of previous infection or vaccination were inoculated with 10 TCID50 of a wild-type virus (SARS-CoV-2/human/GBR/484861/2020) intranasally. Two participants were excluded from per protocol analysis due to seroconversion between screening and inoculation. Eighteen (~53%) became infected, with viral load (VL) rising steeply and peaking at ~5 days post-inoculation. Virus was first detected in the throat but rose to significantly higher levels in the nose, peaking at ~8.87 log10 copies/ml (median, 95% CI [8.41,9.53). Viable virus was recoverable from the nose up to ~10 days post-inoculation, on average. There were no serious adverse events. Mild-to-moderate symptoms were reported by 16 (89%) infected individuals, beginning 2-4 days post-inoculation. Anosmia/dysosmia developed more gradually in 12 (67%) participants. No quantitative correlation was noted between VL and symptoms, with high VLs even in asymptomatic infection, followed by the development of serum spike-specific and neutralising antibodies. However, lateral flow results were strongly associated with viable virus and modelling showed that twice-weekly rapid tests could diagnose infection before 70-80% of viable virus had been generated. Thus, in this first SARS-CoV-2 human challenge study, no serious safety signals were detected and the detailed characteristics of early infection and their public health implications were shown. ClinicalTrials.gov identifier: NCT04865237.

Publisher

Research Square Platform LLC

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