Something old, something new combine for effective vaccine against parasitic skin disease

COLUMBUS, Ohio – Scientists are planning for Phase 1 human trials of a vaccine they developed by using CRISPR gene-editing technology to mutate the parasite that causes leishmaniasis, a skin disease common in tropical regions of the world and gaining ground in the United States. 

In a series of animal studies, the vaccine protected mice against the disease – including mice with compromised immune systems and mice exposed to the parasite in the same way humans are, through the bite of infected sand flies. 

“If you assure protection in the sand fly model, then you have a good shot at a real vaccine,” said Abhay Satoskar, a co-lead investigator of the work and professor of pathology and microbiology at The Ohio State University. 

The team applied the new technology to the century-old Middle Eastern practice of leishmanization – deliberately introducing the live parasite to the skin to create a small infection that, once healed, leads to life-long immunity against further disease. 

“Live vaccines like that are the best vaccines, but there’s a potential risk of causing serious disease in some people,” Satoskar said. “We refined the concept using modern technology, making a parasite that does not cause clinical disease but allows for induction of immunity.” 

The research was published recently in Nature Communications. 

An estimated 1.5 million new cases of cutaneous leishmaniasis, caused by the Leishmania major parasite, are diagnosed worldwide each year, primarily in tropical and subtropical regions of the world – but also in southern Texas. 

Leishmania in all of its forms is considered a neglected disease, mostly affecting populations in warm-weather developing countries – currently infecting about 12 million in all. But Satoskar noted that with global warming, it’s only a matter of time until the southern United States is considered a subtropical region. 

“As the warmth moves up toward the United States, the disease will move up,” he said. 

The standard treatment of more severe cases can be expensive, require multiple daily drug injections and cause unpleasant side effects, leading to poor patient compliance that allows parasites to develop resistance to the drugs. 

To develop the vaccine, the researchers set out to use CRISPR to edit the genome of Leishmania major. The precision technology enabled the researchers to delete centrin, the gene for a protein that supports the parasite’s physical structure, as well as remove an antibiotic resistance marker gene that is needed to be introduced into the parasite for removal of the centrin gene. 

To cause infection, these parasites hijack immune cells and use those host cells to replicate indefinitely. The study showed that the mutant parasite lacking centrin can still find its way into cells and make copies of itself, but for only a limited amount of time and not at a pace that leads to clinical disease. 

“So we’re essentially using leishmanization. CRISPR allowed us to do that,” Satoskar said. “The parasites are unable to proliferate, so they die. But they persist in the body for eight or nine months, which is long enough to generate acquired immunity.” 

Numerous studies in mice, including immune-deficient animals, showed the mutant parasites did not cause skin lesions, but natural parasites did. In additional experiments, vaccinated and unvaccinated mice were subjected to injections of live parasites and bites from infected sand flies seven weeks after their shots. Ten weeks later, most non-immunized mice developed large skin lesions, but only one vaccinated mouse developed a visible lesion. 

“The multiple animal tests also made sure the genome didn’t revert back to normal,” Satoskar said. “And we found that if a sand fly were to bite at the site of the vaccine and take mutated parasites into the wild, the parasites cannot survive. So it is environmentally safe.” 

The international team of researchers from the United States, Japan, Canada and India is identifying partners to manufacture the vaccine, aiming to begin a Phase 1 clinical trial within two years. Satoskar said the vaccine is likely to cost less than $5 a dose – compared to the $100 to $200 cost for treatment in the hardest-hit countries. 

A much more severe form of the disease, visceral leishmaniasis, affects organs and is fatal if left untreated. The team has been using the same CRISPR technique to mutate the genome of the Leishmania donovani strain that causes visceral leishmaniasis, and preliminary data suggest a safe vaccine could be on the horizon. 

The research was supported by the Global Health Innovative Technology Fund, the Canadian Institutes of Health Research, the U.S. Food and Drug Administration’s Center for Biologics Evaluation and Research, the Intramural Research Program of the National Institutes of Health, the National Institute of Allergy and Infectious Diseases, and the Fonds de recherche du Québec – Santé. 

The study was co-led by Hira Nakhasi of McGill University and Greg Matlashewski of the FDA Division of Emerging and Transfusion Transmitted Diseases. The FDA is a co-owner of two U.S. patents associated with the mutated Leishmania species. 

Other Ohio State co-authors include Noushin Saljoughian and Greta Volpedo.

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Contact: Abhay Satoskar, [email protected]; 614-366-3417

Written by Emily Caldwell, [email protected]; 614-292-8152