Author:
Patel Ami,Walters Jewell,Reuschel Emma L.,Schultheis Katherine,Parzych Elizabeth,Gary Ebony N.,Maricic Igor,Purwar Mansi,Eblimit Zeena,Walker Susanne N.,Guimet Diana,Bhojnagarwala Pratik,Doan Arthur,Xu Ziyang,Elwood Dustin,Reeder Sophia M.,Pessaint Laurent,Kim Kevin Y.,Cook Anthony,Chokkalingam Neethu,Finneyfrock Brad,Tello-Ruiz Edgar,Dodson Alan,Choi Jihae,Generotti Alison,Harrison John,Tursi Nicholas J.,Andrade Viviane M.,Dia Yaya,Zaidi Faraz I.,Andersen Hanne,Lewis Mark G.,Muthumani Kar,Kim J Joseph,Kulp Daniel W.,Humeau Laurent M.,Ramos Stephanie,Smith Trevor R.F.,Weiner David B.,Broderick Kate E.
Abstract
SummaryCoronavirus disease 2019 (COVID-19), caused by the SARS-CoV-2 virus, has had a dramatic global impact on public health, social, and economic infrastructures. Here, we assess immunogenicity and anamnestic protective efficacy in rhesus macaques of the intradermal (ID)-delivered SARS-CoV-2 spike DNA vaccine, INO-4800. INO-4800 is an ID-delivered DNA vaccine currently being evaluated in clinical trials. Vaccination with INO-4800 induced T cell responses and neutralizing antibody responses against both the D614 and G614 SARS-CoV-2 spike proteins. Several months after vaccination, animals were challenged with SARS-CoV-2 resulting in rapid recall of anti-SARS-CoV-2 spike protein T and B cell responses. These responses were associated with lower viral loads in the lung and with faster nasal clearance of virus. These studies support the immune impact of INO-4800 for inducing both humoral and cellular arms of the adaptive immune system which are likely important for providing durable protection against COVID-19 disease.
Publisher
Cold Spring Harbor Laboratory
Cited by
38 articles.
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