The development of
a safe and effective SARS-CoV-2 vaccine is a
public health priority. We designed subunit vaccine candidates using
self-assembling ferritin nanoparticles displaying one of two multimerized
SARS-CoV-2 spikes: full-length ectodomain (S-Fer) or a C-terminal
70 amino-acid deletion (SΔC-Fer). Ferritin is an attractive
nanoparticle platform for production of vaccines, and ferritin-based
vaccines have been investigated in humans in two separate clinical
trials. We confirmed proper folding and antigenicity of spike on the
surface of ferritin by cryo-EM and binding to conformation-specific
monoclonal antibodies. After a single immunization of mice with either
of the two spike ferritin particles, a lentiviral SARS-CoV-2 pseudovirus
assay revealed mean neutralizing antibody titers at least 2-fold greater
than those in convalescent plasma from COVID-19 patients. Additionally,
a single dose of SΔC-Fer elicited significantly higher neutralizing
responses as compared to immunization with the spike receptor binding
domain (RBD) monomer or spike ectodomain trimer alone. After a second
dose, mice immunized with SΔC-Fer exhibited higher neutralizing
titers than all other groups. Taken together, these results demonstrate
that multivalent presentation of SARS-CoV-2 spike on ferritin can
notably enhance elicitation of neutralizing antibodies, thus constituting
a viable strategy for single-dose vaccination against COVID-19.