Malaria vaccine highly effective in small U.S. test

WASHINGTON,  (Reuters) – An experimental malaria vaccine proved highly effective in a small, early-stage clinical trial in people, raising hope in the global effort to combat the deadly disease, U.S. researchers reported yesterday in the journal Science.

“This was something that everybody said was not possible. And here it is,” Navy Captain Judith Epstein, one of the researchers, said in a telephone interview.

“We’re in the first stages now of really being able to have a completely effective vaccine,” said Epstein, who said hopes to see licensing of the vaccine within three to five years.

Malaria, commonly spread by mosquitoes, infected 219 million people in 2010 and killed an estimated 660,000, according to estimates by the World Health Organization. That translates into one child in Africa dying every minute.

“It’s an important proof of concept,” Dr. Anthony Fauci, director of the National Insti-tute of Allergy and Infectious Diseases, said of the clinical trial held from October 2011 to October 2012.

Fauci said the test results were the most promising yet of any experimental vaccine. The vaccine was produced by privately held Sanaria Inc of Maryland.

Fauci resisted calling the trial a breakthrough. He said the test only involved a small number of people and that it was not yet clear how long the vaccine’s protection against malaria would last.

The study involved 57 healthy participants aged 18 to 45 who had never had malaria. Of these, 40 got the vaccine and 17 did not.
“There are several more steps before you can feel comfortable that you have something that might be ready for prime time,” he told Reuters. “So we’re really not there yet, but it’s encouraging to see these very favorable results.”

The vaccine, known as PfSPZ, is made from live but weakened parasites of the species Plasmodium falciparum, the most deadly of the malaria-causing parasites.

To test for safety, those in the vaccine group were split into two groups who received two to six doses of the intravenous vaccine at increasing dose levels. They were followed closely for a week, and the team saw no severe side effects.

To test for effectiveness, the team exposed each study participant – those who got the vaccine and those who didn’t – to bites from five malaria infected mosquitoes.

After a week, volunteers were checked for infection, and those who were infected were treated for malaria. The team found that those who got the higher doses of the vaccine were far less likely to develop malaria that those who got lower doses or were not vaccinated.

In the study, only three of 15 participants who received higher dosages of the vaccine became infected, compared to 16 of 17 participants in the lower dosage group who became infected. Among the 12 participants who were not vaccinated, 11 became infected after exposure to infected mosquitoes.

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