SEATTLE, WASHINGTON—The recipe for ending HIV epidemics seems straightforward. Introduce widespread testing. Immediately put those who test positive on antiretroviral (ARV) drugs, which suppress the virus to undetectable levels so those people won’t infect others. The number of new infections will drop, and the epidemic will peter out.
But massive, costly studies done in the past few years have failed to show this strategy can reliably curb the spread of the virus, to the frustration of researchers. The latest and largest ever study presented here last week at the Conference on Retroviruses and Opportunistic Infections did show a modest benefit. But confusingly, there was almost no decline in infections in the study group where it was most expected.
Ending the HIV/AIDS epidemic may be harder than anticipated, it seems. “ARVs on their own are not the magic bullet,” says Collins Iwuji, an epidemiologist at Brighton and Sussex Medical School in the United Kingdom who helped run one of the earlier studies, a South African treatment as prevention (TasP) trial.
The new study, called Population Effects of Antiretroviral Therapy to Reduce HIV Transmission (PopART), included 1 million adults in Zambia and South Africa. When it began in late 2013, research had shown that ARVs can not only stave off disease, but also prevent people from infecting others. But whether these benefits would translate from an individual to an entire community was unclear.
PopART randomized 21 communities into three arms. One received annual house-to-house HIV testing and immediate treatment for those infected (A); another got the same testing, but treatment followed existing country guidelines and was offered only to HIV-infected people who already had evidence of some immune damage (B); and the third got no intervention from the study (C).
After 3 years, an analysis that sampled more than 12,000 people in each of the three arms found group B had 30% fewer new infections than group C. But in arm A, where presumably even more people were treated, the researchers found only 7% fewer infections than in arm C, which wasn’t a statistically significant difference. “When we first saw the results we thought it was the other way around, that arm A and B results got reversed,” says Richard Hayes of the London School of Hygiene & Tropical Medicine, who headed PopART. “We had four statisticians review the data. It’s true I’m afraid.”
“We have a lot of work to do” to explain the unexpected outcome, he adds. Among the factors that could have boosted the infection risk in A are migration of infected people, clustering of sexual networks that had highly infectious individuals, or more sexual risk taking.
François Dabis, who heads the French Agency for Research on AIDS and Viral Hepatitis in Paris and was the principal investigator of the earlier TasP study, says he’s heartened that PopART at least found an impact in arm B. TasP compared immediate treatment with treatment according to South African guidelines; the results, published last year, showed no population benefit from immediate treatment at all, likely because many people who tested positive didn’t seek the free care available.
SEARCH, a large study staged in Kenya and Uganda that used health fairs to do community-wide testing, had more success getting infected people on treatment. But SEARCH investigators reported last summer that they, too, had come up empty-handed. In the middle of the trial, the two countries adopted new World Health Organization (WHO) guidelines recommending that all HIV-infected people get treatment immediately, effectively robbing the study of its control group. (WHO’s recommendations complicated analyses in PopART and TasP as well.) A fourth study in Botswana did find a 30% drop in new cases from widespread testing and treatment, but it had far fewer people and barely reached statistical significance.
Diane Havlir of the University of California, San Francisco, one of SEARCH’s principal investigators, welcomes one clear message from the studies: that widespread testing has the power to identify the majority of infected people, an essential component of the “Ending AIDS” agenda. “We are one step closer and have data for the next steps,” Havlir says.
Nor is anyone ready to give up on universal treatment. “We’re not going in the wrong direction,” Dabis says. “What we’re saying is it’s more complex to achieve reductions in incidence than we anticipated.” Like many others, he says offering ARVs as pre-exposure prophylaxis to people at high-risk of infection is a key missing component of these studies.