A radical new strategy for fighting HIV-AIDS

December 04, 2008

Aidsneedles175     Sorry to disappoint you, but we’re doing a deadly serious topic this week. And I mean that literally, as well as figuratively. Over the past three decades, the AIDS pandemic has become one of the biggest health crises in the history of our planet. According to the U.K.-based humanitarian group AVERT, the disease already has killed more than 25 million people, and an estimated 33 million more are infected with HIV, the virus that causes it. Alarmingly, despite international public health efforts to stem the spread of the disease —such as the promotion of safe sex and attempts to curb needle sharing by IV drug users  —  an estimated 2.7 million more people become infected annually worldwide. Scientists have managed to develop antiretroviral therapy (ART) that, if taken conscientiously on a daily basis, can keep the amount of HIV in the body low and, in a best-case scenario, may enable a person to live for many years without becoming ill.

But wait, there's more...

But virtually everyone has assumed the real answer to HIV-AIDS would come when scientists eventually developed a silver bullet — an anti-HIV vaccine that would prevent a person from becoming infected, and/or would help the body of an infected person to kill the virus. But after 20 years of research, the effort is pretty much stymied, after the failed clinical trial of Merck’s V520 experimental vaccine. In a Scientific American interview this summer, Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases, admitted that researchers are “swimming in the dark,” and explained why such a vaccine has proven so elusive.

Astoundingly, of the tens of millions of people who have been infected, there's not a single documented case of someone who has established infection and ultimately eradicates the virus from the body. There are a number of people who are what we call "long-term nonprogressors"—for one reason or another, perhaps their genetic makeup, they seem to handle the virus reasonably well for a long period of time. For the overwhelming majority of people, the virus ultimately overcomes their immune system's attempts to curtail the virus. So, we are dealing with a situation where we don't even know if the body is capable of eliciting a protective immune response. And if it can, we know it's very difficult, because when you look at infected people, it is so unusual to see people with very good, broadly reacting neutralizing antibodies. So, when you go after developing a vaccine for HIV, you're in an entirely different ballpark than you are when you're trying to develop a vaccine for influenza or smallpox or polio or measles.

We as a field didn't fully appreciate that early on, as a matter of fact. That's the reason why it would be an understandable statement, though now retrospectively clearly premature, to say, "Okay, we have the virus in our hand, we are growing it, we know what it is. It should be a snap to develop a vaccine." Now we know that this just is not the case, so our challenge for the future is to do much better than what natural infection does because natural infection clearly is not successful in inducing an ultimately protective response.

    Sounds grim, doesn’t it? But maybe not. A team of World Health Organization researchers led by physician and biostatistician Reuben M. Granich have just published a  study in the Lancet, a prestigious British medical journal, which suggests a completely different approach. In a greatly oversimplified version, here it is: What if we got everyone — or at least, everyone in developing countries with high HIV infection rates  —   to voluntarily take an HIV test, and then immediately began treating everyone who tested positive with ART, even if they weren’t yet sick? Could such super-aggressive screening and treatment stop the disease’s spread, even without a vaccine? The logic behind this action plan is that treating infected people with antiretroviral drugs can dramatically decrease the “viral load,” i.e. the amount of the virus in their bloodstreams — a major factor in the risk of both heterosexual HIV transmission and mother-to-child transmission of HIV.
    The researchers used data from South Africa  — a nation where about one in five adults is infected, due in large part to in-denial government  —  as a test case for a generalized epidemic.  When they ran the statistical modeling, the results were startling. An an Associated Press story  on the study distills the key points:

Within 10 years, HIV infections dropped by 95 percent. Other initiatives like safe sex education and male circumcision were also used. The strategy would cut the estimated number of AIDS deaths between 2008 and 2050 by about half, from about 8.7 million to 3.9 million, leaving only sporadic HIV cases.

Charles F. Gilks, one of the study’s authors and the chairman of the international health program at Imperial College in London, told the AP:

"In a relatively short amount of time, we could potentially knock the epidemic on its head."

   

    As the Washington Post notes, attacking HIV-AIDS in this energetic fashion might actually cost less, in the long run, than the existing approach:


The strategy would require large up-front investment in testing and treatment but would eventually cost less than the current strategy of putting off treatment until the infection has advanced because so many new infections would be averted. The model assumes testing, drugs and clinical management would cost about $730 a year per patient with first-line drugs, and $3,300 when a person switched to more expensive second-line drugs. By 2032, the cost of the current strategy or delayed treatment and the cost of universal treatment would be about the same: $1.7 billion a year.

    But such a bold idea is not without some downsides. Handing out antiretroviral drugs to everyone who tests positive might accelerate the rise of drug-resistant strains of HIV. Already, public health experts are worried about the prospect of HIV mutating to become resistant to nevirapine, a medication widely used in developing countries to prevent mother-to-child HIV transmission.

Others question whether advising HIV positive people to start treatment immediately, even if they aren’t sick, is ethical, since it may benefit the population as a whole more than it benefits an individual patient. Long-term use of antiretroviral drugs, after all, is known to have potentially dangerous side effects, including liver and muscle cell damage and cardiovascular problems. And because people in developing countries are more likely to suffer also from conditions such as anemia, malnutrition and tuberculosis, they run a higher risk of jeopardizing their health from participating in ART than people in the U.S. and Western Europe do.  It also should be mentioned that getting ART reduces, but doesn’t totally eliminate, the risk of transmitting the virus to someone else. So even if a massive anti-HIV treatment campaign is waged, it’ll still be critical to promote condom use and convince IV drug addicts not to share needles, among other measures.

So what do you think? Is the test-everybody, treat-everybody strategy the way to go? Or should we continue to hold out our hopes for that elusive HIV vaccine? Express your opinion below.


Patrick J. Kiger has written for print publications ranging from GQ to the Los Angeles Times Magazine, and is the co-author of two books, Poplorica: A popular history of the fads, mavericks, inventions and lore that shaped modern America," and Oops: 20 life lessons from the fiascoes that shaped America. For more of his work, check out his web site, www.patrickjkiger.com.
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