Researchers said for the first time an experimental vaccine has cut the risk of infection with the deadly Aids virus.
US military and Thai health officials told a news conference today in Bangkok that the vaccine cut the risk of becoming infected with HIV by more than 31%.
The result came after the world’s largest Aids vaccine trial of more than 16,000 volunteers in Thailand.
Recent failures led many scientists to think such a vaccine might never be possible.
Even though the benefit is modest, “it’s the first evidence that we could have a safe and effective preventive vaccine”, military spokesman Jerome Kim said in a telephone interview. He helped lead the study for the US Army, which sponsored it with the National Institute of Allergy and Infectious Diseases.
The institute’s director, Dr Anthony Fauci, warned that this is “not the end of the road” but said he was surprised and very pleased by the outcome.
“It gives me cautious optimism about the possibility of improving this result” and developing a more effective Aids vaccine, Dr Fauci said in a telephone interview. “This is something that we can do.”
Even a marginally helpful vaccine could have a big impact. Every day, 7,500 people worldwide are newly infected with HIV; 2 million died of Aids in 2007, the UN agency UNAids estimates.
“Today marks an historic milestone,” said Mitchell Warren, executive director of the Aids Vaccine Advocacy Coalition, an international group that has worked toward developing a vaccine.
“It will take time and resources to fully analyse and understand the data, but there is little doubt that this finding will energise and redirect the Aids vaccine field,” he said in a statement.
The Thailand Ministry of Public Health conducted the study, which used strains of HIV common in Thailand. Whether such a vaccine would work against other strains in the US, Africa or elsewhere in the world is unknown, scientists stressed.
The study actually tested a two-vaccine combo in a “prime-boost” approach, where the first one primes the immune system to attack HIV and the second one strengthens the response.
They are ALVAC, from Sanofi Pasteur, the vaccine division of French drugmaker Sanofi-Aventis; and AIDSVAX, originally developed by VaxGen, and now held by Global Solutions for Infectious Diseases, a non-profit founded by some former VaxGen employees.
ALVAC uses canarypox, a bird virus altered so it cannot cause human disease, to ferry synthetic versions of three HIV genes into the body. AIDSVAX contains a genetically engineered version of a protein on HIV’s surface. The vaccines are not made from whole virus – dead or alive – and cannot cause HIV.
Neither vaccine in the study prevented HIV infection when tested individually in earlier trials, and dozens of scientists had called the new one futile when it began in 2003.
“I really didn’t have high hopes at all that we would see a positive result,” Dr Fauci confessed.
The results proved sceptics wrong.
“The combination is stronger than each of the individual members,” said the Army’s Mr Kim.
The study tested the combo in HIV-negative Thai men and women ages 18 to 30 at average risk of becoming infected.
Half received four “priming” doses of ALVAC and two “boost” doses of AIDSVAX over six months. The others received dummy shots. No one knew who got what until the study ended.
All were given condoms, counselling and treatment for any sexually transmitted infections, and were tested every six months for HIV. Any who became infected were given free treatment with antiviral medicines.
Participants were followed for three years after vaccination ended.
New infections occurred in 51 of the 8,197 given vaccine and in 74 of the 8,198 who received dummy shots. That worked out to a 31% lower risk of infection for the vaccine group.
The vaccine had no effect on levels of HIV in the blood of those who did become infected. That had been another goal of the study – seeing whether the vaccine could limit damage to the immune system and help keep infected people from developing full-blown Aids.
That result is “one of the most important and intriguing findings of this trial,” Dr Fauci said. It suggests that the signs scientists have been using to gauge whether a vaccine was actually giving protection may not be valid.
“It is conceivable that we haven’t even identified yet” what really shows immunity, which is both “important and humbling” after decades of vaccine research, Dr Fauci said.
Details of the study will be given at a vaccine conference in Paris in October.
This is the third big vaccine trial since 1983, when HIV was identified as the cause of Aids. In 2007, Merck & Co stopped a study of its experimental vaccine after seeing it did not prevent HIV infection. Later analysis suggested the vaccine might even raise the risk of infection in certain men. The vaccine itself did not cause infection.
It is unclear whether vaccine makers will seek to license the two-vaccine combo in Thailand. Before the trial began, the US Food and Drug Administration said other studies would be needed before the vaccine could be considered for US licensing.
Also unclear is whether Thai volunteers who received dummy shots will now be offered the vaccine. Researchers had said they would do so if the vaccine showed clear benefit – defined as reducing the risk of infection by at least 50%.
Those issues, plus how to proceed with future studies, will be discussed among the governments, study sponsors and companies involved in the trial, Mr Kim said. Scientists want to know how long will protection last, whether booster shots will be needed, and whether the vaccine helps prevent infection in gay men and injection drug users, since it was tested mostly in heterosexuals in the Thai trial.
The study was done in Thailand because US Army scientists did pivotal research in that country when the Aids epidemic emerged there, isolating virus strains and providing genetic information on them to vaccine makers. The Thai government also strongly supported the idea of doing the study.