Researchers at NYU Langone Medical Center and elsewhere say that a vaccination they have developed to fight a brain wasting syndrome in deer and other animals may hold promise on two additional fronts: protecting U.S. livestock from contracting the disease, and preventing similar brain infections in humans.
The study, published online in Vaccine Dec. 21, documents a scientific milestone: the first successful vaccination of deer against chronic wasting disease (CWD), a fatal brain disorder caused by unusual infectious proteins known as prions. Prions propagate by converting otherwise healthy proteins into a disease state.
Equally important, the researchers said, this study may hold promise against human diseases suspected of being caused by prion infections, such as Creutzfeldt-Jakob disease, kuru, familial insomnia and variably protease-sensitive prionopathy. Some studies also have associated prion-like infections with Alzheimer's disease.
"Now that we have found that preventing prion infection is possible in animals, it's likely feasible in humans as well," said senior study investigator and neurologist Thomas Wisniewski, a professor at NYU Langone.
CWD afflicts much of North America's captive deer population, as well as large numbers of other cervids that populate the plains and forests of the Northern Hemisphere, including wild deer, elk, caribou and moose. There is growing concern among scientists that CWD could possibly spread to livestock in the same regions, especially cattle, in much the same manner that bovine spongiform encephalopathy — another prion-based infection — spread through the U.K. almost two decades ago.
According to Wisniewski and his research team, if further vaccine experiments prove successful, a relatively small number of animals (as few as 10%) could be inoculated to induce herd immunity, in which disease transmission is essentially stopped in a much larger group.
For the study, five deer were given the vaccine; another six were given a placebo. All of the deer were exposed to prion-infected brain tissue. They also were housed together, engaging in group activities similar to those in the wild. The researchers said this kept them in constant exposure to the infectious prions.
The animals receiving the vaccine were given eight boosters over 11 months until key immune antibodies were detectable in the blood, saliva and feces. The deer also were monitored daily for signs of illness, and investigators performed biopsies of the animals' tonsils and gut tissue every three months to search for signs of CWD infection.
Within two years, all of the deer given the placebo developed CWD. Four deer given the vaccine took significantly longer to develop infection, and the fifth one remains infection free.
Wisniewski and his team made the vaccine using salmonella — which easily enters the gut — to mirror the most common mode of natural infection: ingestion of prion-contaminated food or feces. To prepare the vaccine, the team inserted a prion-like protein into the genome of an attenuated, or no longer dangerous, salmonella bacterium. This engineered the salmonella to induce an immune response in the gut, producing anti-prion antibodies.
"Although our anti-prion vaccine experiments have so far been successful on mice and deer, we predict that the method and concept could become a widespread technique for not only preventing but potentially treating many prion diseases," lead study investigator Dr. Fernando Goni, an associate professor at NYU Langone, said.
Funding for the study was provided by the National Institutes of Health and the Seix Dow Foundation.