| Literature DB >> 33823303 |
Ruklanthi de Alwis1, Esther S Gan2, Shiwei Chen2, Yan Shan Leong3, Hwee Cheng Tan2, Summer L Zhang2, Clement Yau2, Jenny G H Low4, Shirin Kalimuddin5, Daiki Matsuda6, Elizabeth C Allen6, Paula Hartman6, Jenny Park6, Maher Alayyoubi6, Hari Bhaskaran6, Adrian Dukanovic6, Yanjie Bao6, Brenda Clemente6, Jerel Vega6, Scott Roberts6, Jose A Gonzalez6, Marciano Sablad6, Rodrigo Yelin6, Wendy Taylor6, Kiyoshi Tachikawa6, Suezanne Parker6, Priya Karmali6, Jared Davis6, Sean M Sullivan7, Steve G Hughes6, Pad Chivukula6, Eng Eong Ooi1.
Abstract
A self-transcribing and replicating RNA (STARRTM) based vaccine (LUNAR®-COV19) has been developed to prevent SARS-CoV-2 infection. The vaccine encodes an alphavirus-based replicon and the SARS-CoV-2 full length spike glycoprotein. Translation of the replicon produces a replicase complex that amplifies and prolong SARS-CoV-2 spike glycoprotein expression. A single prime vaccination in mice led to robust antibody responses, with neutralizing antibody titers increasing up to day 60. Activation of cell mediated immunity produced a strong viral antigen specific CD8+ T lymphocyte response. Assaying for intracellular cytokine staining for IFN-γ and IL-4 positive CD4+ T helper lymphocytes as well as anti-spike glycoprotein IgG2a/IgG1 ratios supported a strong Th1 dominant immune response. Finally, single LUNAR-COV19 vaccination at both 2 μg and 10 μg doses completely protected human ACE2 transgenic mice from both mortality and even measurable infection following wild-type SARS-CoV-2 challenge. Our findings collectively suggest the potential of LUNAR-COV19 as a single dose vaccine.Entities:
Keywords: COVID-19; Coronavirus; LUNAR®-COV19; SARS-CoV-2; STARRTM; Vaccine; conventional mRNA; self-amplifying RNA
Year: 2021 PMID: 33823303 DOI: 10.1016/j.ymthe.2021.04.001
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454