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Could this 'super vaccine' prevent cancer?


According to a study published in Cell Reports Medicine, a new nanoparticle-based vaccine can successfully prevent several types of aggressive cancers in mice, with almost 90% of mice staying tumor-free depending on the type of cancer. 

Study details and key findings

Two primary elements of vaccines are antigens and adjuvants. An antigen is a portion of a disease-causing pathogen that the immune system is primed to recognize and eliminate. An adjuvant is an ingredient that can increase the immune response to an antigen.

"In recent years, we have come to understand how important the selection of the adjuvant is because it drives the second signal that is needed for the correct priming of T and B [immune] cells," said Prabhani Atukorale, an assistant professor of biomedical engineering at the University of Massachusetts Amherst's Riccio College of Engineering.

Previously, Atukorale developed a lipid nanoparticle-based drug design that could shrink or eliminate tumors in mice. In the new study, researchers used the nanoparticle system to encase the adjuvants and melanoma peptide antigens in a vaccine combination, which was then given to mice. After three weeks, the mice were exposed to melanoma cells.

Overall, 80% of the mice who were vaccinated with the "super adjuvant" nanoparticle vaccine remained tumor-free until the end of the study, which lasted 250 days. In comparison, mice that were unvaccinated or had been vaccinated with a non-nanoparticle formulation developed tumors, and none survived past 35 days.

The mice who received the nanoparticle vaccine were also protected against the spread of cancer to their lungs. All the other mice in the study developed tumors in their lungs.

"Metastases across the board is the highest hurdle for cancer," Atukorale said. "The vast majority of tumor mortality is still due to metastases, and it almost trumps us working in difficult-to-reach cancers, such as melanoma and pancreatic cancer."

The researchers also conducted a second experiment where they combined the nanoparticles with tumor lysate as the new antigen. Tumor lysate refers to killed cancer cells that are taken directly from a tumor mass.

After being vaccinated with the nanoparticle lysate vaccine, the mice were exposed to either melanoma, triple-negative breast cancer, or pancreatic ductal adenocarcinoma cells. Overall, 88% of the mice exposed to pancreatic cancer remained tumor-free, as well as 75% of mice exposed to breast cancer, and 69% of mice exposed to melanoma. All mice that remained tumor-free after vaccination also resisted metastasis when exposed to cancer cells.

"The tumor-specific T-cell responses that we are able to generate -- that is really the key behind the survival benefit," said Griffin Kane, postdoctoral research associate at UMass Amherst and the study's lead author. "There is really intense immune activation when you treat innate immune cells with this formulation, which triggers these cells to present antigens and prime tumor-killing T cells."

Commentary

According to the researchers, the nanoparticle design provides a platform approach that could be applied to several different types of cancers.

"By engineering these nanoparticles to activate the immune system via multi-pathway activation that combines with cancer-specific antigens, we can prevent tumor growth with remarkable survival rates," Atukorale said.

In the future, the researchers hope that the platform can be used to develop both therapeutic and preventive cancer treatments, particularly for people who have a high risk of cancer. To expand the research into this technology, Atukorale and Kane have partnered together on a startup called NanoVax Therapeutics.

"The real core technology that our company has been founded on is this nanoparticle and this treatment approach," Kane said. "This is a platform that Prabhani developed. The startup lets us pursue these translational efforts with the ultimate goal of improving patients' lives."

Currently, Atukorale and Kane are working to extend this technology to a therapeutic vaccine and have taken the initial steps to de-risk the technology in translation.

(ScienceDaily, 10/13; Millington, Newsweek, 10/13; University of Massachusetts Amherst news release, 10/9; Boulter, Cosmos, 10/13)


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