Now scientists at The Wistar Institute have developed a more targeted vaccine that, in animal studies, shows stronger, broader, and more durable protection in a single, low dose.
In addition to its other advantages, the vaccine could be stored at room temperature, making it potentially easier to transport to remote or developing locations than existing mRNA vaccines, which require specialized cold storage.
“This is among the first next-generation vaccines that will have more advanced features and broader protection,” said Daniel Kulp, PhD, associate professor in the Vaccine & Immunotherapy Center at The Wistar Institute and corresponding author of the study.
The paper, “Nucleic acid delivery of immune-focused SARS-CoV-2 nanoparticles drive rapid and potent immunogenicity capable of single-dose protection,” was published in the journal Cell Reports.
Existing vaccines include an unmodified receptor binding domain of SARS-CoV-2 spike protein.
The new vaccine consists of a rationally engineered receptor binding domain using computational and structure-based design methodologies. The engineered receptor binding domain blocks ‘immune distracting’ sites and can therefore elicit more potent levels of protective, neutralizing antibodies.
Researchers then naturally self-assembled proteins to form nanoparticles that display these highly engineered immunogens.
By arranging themselves into structures that resemble an actual virus, the nanoparticles are more easily recognized by the immune system and transported to the germinal centres, where they activate B cells which produce protective antibodies.
Using nucleic acid vaccine delivery technology similar to mRNA, the nanoparticle vaccine is encoded in DNA and delivered into cells, giving the body genetic instructions to build the immunogen internally.
This is an advance over traditional vaccines that must be manufactured in specialized factories through complex vaccine production processes. In contrast to other vaccines, Dr Kulp noted that one advantage of the DNA platform is that it doesn’t require refrigeration. It can also be quickly reformulated to target new variants.
In animal models, researchers found that the DNA delivered immune-focused nanoparticle vaccine produced much higher levels of neutralizing antibodies than the vaccine that wasn’t immune-focused.
“A difficulty with current vaccines is that neutralizing antibodies decline over time,” Kulp said. The nanoparticle vaccine produced durable responses after a single immunization for six months in mice, unlike what we see with current SARS-CoV-2 vaccines in people.
The ultimate test for SARS-CoV-2 vaccine candidates is protection from death in SARS-CoV-2 challenge experiments.
In a lethal challenge model, the researchers found that 100% of mice who received the immune-focused nanoparticle vaccine were protected from death with a single low dose. Most mice who received the standard, non-immune focused vaccine died within ten days of the challenge.
They conducted the vaccine assessment in both wild-type mice and mice that were genetically engineered to mimic human immune systems, he noted.
Even without being updated, the immune-focused vaccine showed a comparable level of antibody production to Delta and other variants, Kulp said.
That’s partly because of the immune focusing approach itself.
He noted; that blocking parts of the receptive binding domain to inhibit non-neutralizing antibodies, it also blocks many of the areas affected by spike protein mutations. Studies on the Omicron variant are underway.
Researchers are seeking funding to begin human trials of the vaccine.
Co-author David B. Weiner, PhD, executive vice president, director of the Vaccine & Immunotherapy Center and the W.W. Smith Charitable Trust Professor in Cancer Research, at The Wistar Institute, said the vaccine could provide a needed step forward to improve protection against COVID-19.
“Current vaccine effects on reducing transmission of SARS-CoV-2 variants of concern including Delta and Omicron could be improved for their breadth of protection as well as their immune potency,” Weiner said.
“This study demonstrates that using a nucleic acid approach combined with in vivo structural assembly of a glycan immune-focused nanoparticle drives single protection and neutralization against diverse variants of concern in a dose-sparing formulation. Additional studies of this vaccine approach for SARS-CoV-2 appear timely and important.”
Source: Medindia
