Eric Gowans of the Adelaide University said the vaccine has already seen positive results in animals, with human trials to start next year, an ABC report said.
"DNA vaccines in general have enormous potential, but have not worked very well in large animals and in patients," Gowans said.
"They work very nicely in mice and we have developed a protocol and a technique that simplifies the whole process and makes a DNA vaccine very much more effective in large animals," he said, and added that he has found a way to stimulate the body's immune system response which helps deliver the vaccine.
"Because we want to improve the efficacy of the DNA vaccination, we target the skin because the skin has a much greater proportion of white blood cells, which are important for the kind of immunity that we are trying to impart," he said.
Those white blood cells are known as dendritic cells and play a key role during infection and vaccination.
The DNA vaccine stimulates the body's immune response and combines with the white blood cells to kill HIV or hepatitis C cells.
"What we need to do is to target that small population of white blood cells, which circulate generally in the body, and unless the vaccine targets those cells, the vaccine isn't effective and isn't efficient in any way," Gowans said.
Gowans said other researchers have used skin to deliver the vaccine, but not to target white blood cells in this way.
"We kill the cells that the vaccine is targeted to, and then those dead cells are highly inflammatory and they attract more of these white blood cells, so that is the difference," he said.
While the vaccine is currently designed to treat patients who already have hepatitis C, Gowans said, it is likely, it could be used as a preventative vaccine for hepatitis C and HIV in the next five years.
"I don't want to be too optimistic, but I think when we do the clinical trial next year, I think we can then begin to work out how best to take it forward from there.
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