The road to a cure for HIV/AIDS

Something wonderful sometimes happens when scientists and the public get together to talk about research. All the jargon, all the technical language falls away and it becomes instead a conversation between the two groups with most at stake, the people in need of a treatment or cure, and the people trying to develop it.

HIV Matters Town Hall, West Hollywood

HIV Matters Town Hall, West Hollywood

Last week CIRM joined with the AIDS Project Los Angeles to hold a Town Hall event in West Hollywood called HIV Matters: Countdown to a Cure: California Leads the Way. Around 120 people showed up to listen to stem cell scientists from City of Hope, University of Southern California (USC), Calimmune, and Sangamo Biosciences all of whom are using CIRM funding to develop new treatments, hopefully even cures, for HIV/AIDS.

Just a few years ago an event like this would have been unthinkable. The idea of talking about curing HIV/AIDS would have opened you up to ridicule and accusations of hyping the science. Today CIRM is funding three projects that have been approved for clinical trials (you can read about those here, here and here) and other research that is pushing the boundaries of our knowledge in search of even better approaches.

As David Hardy, the Chief Medical Officer for Calimmune, said:

“What is exciting today is that cure is now something that can be talked about as a potential reality.”

After brief presentations to discuss their work and the science behind it the panel opened the event up to questions from the audience.

Panel L to R: John Zaia, Dale Ando, David Hardy, Paula Cannon

Panel L to R: John Zaia, Dale Ando, David Hardy, Paula Cannon

One of the first questions silenced the room. “Is death a possible side effect of these clinical trials?”

Dr. John Zaia, the Chief of Virology at City of Hope near Los Angeles (and the lead investigator on one of the clinical trials) answered without any hesitation. “Yes”.

“We do everything we can to limit all side effects, especially the most extreme ones, but we have to be honest with patients and explain it is a remote possibility. That’s why it is covered in the informed consent process that every person goes through before signing up for the trial. We want to make sure everyone completely understands what they are signing up for.”

Dr. Dale Ando, Chief Medical Officer at Sangamo BioSciences, talked about the other approaches that are currently being explored to kill the AIDS virus, such as “shock and kill”, where a combination of drugs flushes the virus from hidden reservoirs in the body and then a boost to the immune system kills it.

Paula Cannon, PhD., a CIRM grantee and stem cell scientist at the Keck School of Medicine at USC, talked about her research aimed at developing the next generation of stem cell therapy targeting HIV/AIDS.

Current approaches take blood stem cells out of the body, genetically modify them so they are resistant to the virus, then return them to create a new blood and improved immune system. Cannon’s work is going to try and do that inside the body, without the need to remove the blood stem cells, in essence copying what the AIDS virus does when it infects cells and using that approach against it, creating a one-stop anti-viral approach to kill HIV.

It’s an audacious idea. But sometimes audacity is what you need to make big changes.

CIRM Board member and Patient Advocate for HIV/AIDS, Jeff Sheehy, moderated the discussion and ended the evening with a tribute to all the people who volunteered to be part of these, and every, clinical trial.

“They know, particularly in these early stage clinical trials where the focus is just showing that this approach is safe, that they are not likely to experience any benefit themselves. But they still volunteer, because they want to be part of something that could help many others. There’s a real sense of altruism. They want to advance the science.”

And the science is advancing. Maybe not always as fast as everyone would hope but we are making progress. And with each advance we get one step closer to our ultimate goal, of advancing stem cell therapies to patients with unmet medical needs.

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