Safety and immunogenicity of a self-amplifying RNA vaccine against COVID-19: COVAC1, a phase I, dose-ranging trial

Katrina M. Pollock(NIHR Imperial Biomedical Research Centre), Hannah M. Cheeseman(Imperial College London), Alexander J. Szubert(MRC Clinical Trials Unit at UCL), Vincenzo Libri(UCL Biomedical Research Centre), Marta Boffito(Chelsea and Westminster Hospital), David R. Owen(NIHR Imperial Biomedical Research Centre), Henry Bern(MRC Clinical Trials Unit at UCL), Leon R. McFarlane(Imperial College London), Jessica O’Hara(Imperial College London), Nana‐Marie Lemm(Imperial College London), Paul F. McKay(Imperial College London), Tommy Rampling(UCL Biomedical Research Centre), Yee Ting Nicole Yim(UCL Biomedical Research Centre), Ana Milinkovic(Chelsea and Westminster Hospital), Cherry Kingsley(Imperial College London), Tom Cole(NIHR Imperial Biomedical Research Centre), Susanne Fagerbrink(NIHR Imperial Biomedical Research Centre), Marites Aban(NIHR Imperial Biomedical Research Centre), Maniola Tanaka(NIHR Imperial Biomedical Research Centre), Savviz Mehdipour(NIHR Imperial Biomedical Research Centre), Alexander J. Robbins(NIHR Imperial Biomedical Research Centre), William Budd(NIHR Imperial Biomedical Research Centre), Saul N. Faust(University Hospital Southampton NHS Foundation Trust), Hana Hassanin(University of Surrey), Catherine A. Cosgrove(St George's, University of London), Alan Winston(Imperial College London), Sarah Fidler(Imperial College London), David Dunn(MRC Clinical Trials Unit at UCL), Sheena McCormack(MRC Clinical Trials Unit at UCL), Robin J. Shattock(Imperial College London), Kirsty Adams, Fahimah Amini, Nafisah B Atako, Amalina Bakri, William Barclay, Elizabeth Brodnicki, Jonathan C. Brown, Ruth A. Byrne, Rowena Chilvers, Sofia Coelho, Suzanne Day, Monica Desai, Eleanor Dorman, Tamara Elliott, Katie E. Flight, James L. K. Fletcher, John Galang, Jagruti Gohil, A. Gupta, Christopher Harlow, Kai Hu, Mohini Kalyan, Dominic Lagrue, Ely Liscano, Cecilia Njenga, Krunal Polra, Derecia A Powlette, Paul Randell(Imperial College London), Mary Rauchenberger, I Redknap, Maravic Ricamara, Paul Rogers(Imperial College London), Hadijatou Sallah, Karnyart Samnuan, Michaël Schumacher, Zareena Shah, Rachel Shaw, Thomas R. Shaw, Stefan Sivapatham, Susie Slater, Kim Sorley, Regina Storch, Elizabeth Tan(NIHR Imperial Biomedical Research Centre), Tricia Tan(NIHR Imperial Biomedical Research Centre), Lieze Thielemans, Sarah Whitely(Imperial College London), Charlotte Valentine, Jeeva Varghese, Asha Vikraman, Martin R. Wilkins
EClinicalMedicine
January 14, 2022
Cited by 158Open Access
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Abstract

BACKGROUND: Lipid nanoparticle (LNP) encapsulated self-amplifying RNA (saRNA) is a novel technology formulated as a low dose vaccine against COVID-19. METHODS: October 2020. Participants received two intramuscular (IM) injections of LNP-nCoVsaRNA at six different dose levels, 0.1-10.0μg, given four weeks apart. An open-label dose escalation was followed by a dose evaluation. Solicited adverse events (AEs) were collected for one week from enrolment, with follow-up at regular intervals (1-8 weeks). The binding and neutralisation capacity of anti-SARS-CoV-2 antibody raised in participant sera was measured by means of an anti-Spike (S) IgG ELISA, immunoblot, SARS-CoV-2 pseudoneutralisation and wild type neutralisation assays. (The trial is registered: ISRCTN17072692, EudraCT 2020-001646-20). FINDINGS: 192 healthy individuals with no history or serological evidence of COVID-19, aged 18-45 years were enrolled. The vaccine was well tolerated with no serious adverse events related to vaccination. Seroconversion at week six whether measured by ELISA or immunoblot was related to dose (both p<0.001), ranging from 8% (3/39; 0.1μg) to 61% (14/23; 10.0μg) in ELISA and 46% (18/39; 0.3μg) to 87% (20/23; 5.0μg and 10.0μg) in a post-hoc immunoblot assay. Geometric mean (GM) anti-S IgG concentrations ranged from 74 (95% CI, 45-119) at 0.1μg to 1023 (468-2236) ng/mL at 5.0μg (p<0.001) and was not higher at 10.0μg. Neutralisation of SARS-CoV-2 by participant sera was measurable in 15% (6/39; 0.1μg) to 48% (11/23; 5.0μg) depending on dose level received. INTERPRETATION: Encapsulated saRNA is safe for clinical development, is immunogenic at low dose levels but failed to induce 100% seroconversion. Modifications to optimise humoral responses are required to realise its potential as an effective vaccine against SARS-CoV-2. FUNDING: This study was co-funded by grants and gifts from the Medical Research Council UKRI (MC_PC_19076), and the National Institute Health Research/Vaccine Task Force, Partners of Citadel and Citadel Securities, Sir Joseph Hotung Charitable Settlement, Jon Moulton Charity Trust, Pierre Andurand, Restore the Earth.


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