This article originally appeared in HIV Treatment Update, a newsletter published by NAM between 1992 and 2013.
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In April’s HTU, we featured a news story, reporting that a group of patients had had their CD4 counts boosted by a form of gene therapy – and declaring that this could be the first step to a cure for HIV infection.1Matt Sharp wrote an article on lymphoma for that same issue. What we didn’t tell you is that he was one of the six participants in the gene experiment and so far, he writes, it seems to be working just fine.

Gene therapy – the process of manipulating human genetic material in order to slow and stop disease and interfere with disease processes – is no longer science fiction for people with HIV. While there is more to learn and the research is new, gene therapy may lead to what is known as a ‘functional HIV cure’ by modifying part of the body’s own genetic code in order to make cells resistant to HIV. If a functional cure is successful, the damage HIV causes could be halted without the use of antiretroviral drugs.

My personal story intersects perfectly with the advent of HIV gene therapy. I have been living with HIV almost half my life, since I was diagnosed in 1988, surviving with a mixture of resilience and determination to live.

Glossary

CD4 cells

The primary white blood cells of the immune system, which signal to other immune system cells how and when to fight infections. HIV preferentially infects and destroys CD4 cells, which are also known as CD4+ T cells or T helper cells.

gene

A unit of heredity, that determines a specific feature of the shape of a living organism. This genetic element is a sequence of DNA (or RNA, for viruses), located in a very specific place (locus) of a chromosome.

CCR5

A protein on the surface of certain immune system cells, including CD4 cells. CCR5 can act as a co-receptor (a second receptor binding site) for HIV when the virus enters a host cell. A CCR5 inhibitor is an antiretroviral medication that blocks the CCR5 co-receptor and prevents HIV from entering the cell.

gene therapy

A type of experimental treatment in which foreign genetic material (DNA or RNA) is inserted into a person's cells to prevent or fight disease.

cure

To eliminate a disease or a condition in an individual, or to fully restore health. A cure for HIV infection is one of the ultimate long-term goals of research today. It refers to a strategy or strategies that would eliminate HIV from a person’s body, or permanently control the virus and render it unable to cause disease. A ‘sterilising’ cure would completely eliminate the virus. A ‘functional’ cure would suppress HIV viral load, keeping it below the level of detection without the use of ART. The virus would not be eliminated from the body but would be effectively controlled and prevented from causing any illness. 

Clearly, antiretroviral (ARV) drugs have kept me alive and relatively healthy. I was always keen to benefit from what medicine could do for me, and enrolled in several early-access programmes and clinical trials of unproven drugs in the late ‘80s and ‘90s.

Back then I didn’t have the choices we have today, with now more than two dozen antiretroviral drugs available. As drugs were approved one at a time, many people added a new drug to an older one they were taking, which we now understand leads to resistance. I always managed to stay ahead of the latest treatments, but since it was unclear how to best use the drugs in the early days of HIV, I developed resistance to almost every drug and now have a fragile immune system with few new treatment options in my future. Fortunately, the drugs were just useful enough to keep my health stable, but until quite recently I never achieved an undetectable viral load and my CD4 cells bottomed out at 30 cells/mm3. The good news is that, thanks to careful monitoring, I never had an AIDS-defining infection.

I’m now thriving. In 2008 I was finally able to combine two new antiretroviral drugs that I had never tried before and reached undetectable HIV levels, remaining that way since then. But my CD4 cells remained stubborn, rarely crossing over the 200 cells/mm3 benchmark that defines AIDS in the US, where I live.

I have never been reticent about participation in clinical trials. Back in the ‘90s, many people enrolled in studies just to get access to the latest drugs. I even signed up for a study looking at thymus transplantation, which involved opening my abdomen in a surgical procedure. People thought I was brave, if not a bit crazy, but I have always felt that if I sat around and waited for the research to prove successful, I would not survive.

My personal story intersects perfectly with the advent of HIV gene therapy. I have been living with HIV almost half my life, since I was diagnosed in 1988, surviving with a mixture of resilience and determination to live.

Since the days of ACT UP Golden Gate when, as a dedicated treatment activist, I was arrested seven times in civil disobedience protests, I have sought immune-based therapies and advocated for research that would focus on CD4 cells, HIV’s target. Until recently there have been no successful immune-based therapy studies to restore the CD4 cells in people with HIV. Two huge and expensive efforts, the ESPRIT2 and SILCAAT3 trials, used a synthetic version of interleukin-2 (IL-2), a naturally occurring protein also known as T-cell growth factor. Unfortunately, despite early promise in boosting important CD4 cells in trial participants, the treatment was found to be difficult to tolerate and in the end, ineffective. Before the study results came out, a doctor prescribed IL-2 for me. My CD4 count increased to over 600 cells/mm3 from a low of 140 cells/mm3, but in about a month they dropped back to where I started. Another failed treatment attempt!

But today I may have hope for restoration of my immune system, or at the very least an expansion of CD4 cells. In 2009, I visited the Quest Research Clinic in San Francisco and met with Jay Lalezari, MD, a research physician I have known since the days of ACT UP Golden Gate.

He told me that his clinic was testing a new gene therapy technology called SB728. This is an enzyme from a family called zinc finger nucleases (ZFNs), which could theoretically make CD4 cells resistant to HIV. The ZFNs are like tiny molecular ‘scissors’ that cut out the CCR5 gene. This gene provides CD4 cells with the CCR5 molecule, a ‘co-receptor’ protein that studs CD4 cell surfaces and which is an essential anchoring point for the most common form of HIV. Cells without the CCR5 co-receptor are effectively protected from HIV infection.

After speaking with several treatment activists and researchers including Dr Jay, as he is affectionately known, I decided the risk was low and wanted to try it out. So far, six months later, it appears the strategy is at the least safe, if not showing some positive effects.

I enrolled in the study in the summer of 2010 and flew to Los Angeles for what is called an apheresis procedure. In this, you get hooked up to an oven-sized machine that removes blood and separates the cell types within it. First, an intravenous needle was placed in each of my arms; blood was removed from one arm and infused into the machine where it separated out the white cells (including CD4 cells). The remaining red blood cells were then replaced into my other arm. By the end of the procedure, only a small infusion bag a quarter full of blood had been taken from my arm. The apheresis was effortless and I was out of the clinic in a few hours.

The simplest explanation of the next steps of the process goes something like this. My white blood cells were sent to the laboratory and the CD4 cells were separated, made to replicate so there were more of them, and processed with the zinc finger nucleases to remove their CCR5 gene. The ZFNs were delivered to my cells inside the test tube enclosed in something called an adenovirus vector: the hollowed-out shell of a common cold virus, which is able to enter cells and deliver its contents to a cell’s nucleus, but cannot cause an infection.

The newly modified cells were then frozen, sent to the study clinic, thawed and infused back into my arm – four billion of them. I experienced no side-effects during the 30-minute infusion.

My own results have been quite exciting given my lacklustre treatment history. My CD4 cell count doubled from 230 to 560 cells/mm3. Now, six months later, my CD4 cells have remained at the higher level and I feel better than ever. I have had virtually no long-term side-effects, though I have had to endure extensive blood tests to follow up on my blood results.

Also, and less comfortably, the study has required rectal biopsies to see if the manipulated cells ‘traffic’ to the gut. This is important as it shows that the modified cells are acting exactly like other immune cells and successfully competing with them. It is also potentially exciting, since it is through CCR5-bearing cells in the mucous membranes of the genital and digestive systems that most people are infected with HIV. I have had about six 30-minute biopsy procedures, cutting 20 tissue samples from inside my sigmoid colon each time. The biopsies are relatively painless, save the amount of gas that’s pumped in the colon so the doctor can remove the tissue with a tiny instrument. I have not learned the results of my own biopsies so far, but the other participants are showing good results.

Manipulating DNA, the genetic blueprint, through gene therapy can be risky but has been safely studied in cancer and degenerative diseases. This is not the first HIV-related gene therapy trial, but it is the first to show promise. Dr Lalezari recently presented data from the study I enrolled in at the Conference on Retroviruses and Opportunistic Infections (CROI) in Boston in February. He presented data on SB728 in six men who have been living with AIDS for over twenty years.4

This first study proved the gene therapy concept, and I experienced a CD4 boost, but there was never any danger of my HIV running out of control as I remained on antiretrovirals. The second study will enrol people who are not taking antiretroviral therapy

Dr Jay told me: “The study has shown seven things: logistically we can effectively get peripheral blood mononuclear cells [white cells inhabiting the blood] out of the body; the cells can be modified; the infusion is safe; the participants have shown an increase in CD4 cells; the cells persist and don’t die off; and they traffic to the gut.

“The final thing is that there is also normalisation of the CD4:CD8 ratio.”

This is particularly significant, because nearly all people with HIV, even with high CD4 counts, have about twice as many CD8 cells (the cells that kill off virus-infected cells) as CD4 cells (which direct a lot of the traffic of the immune system). In HIV-negative people the situation is the opposite, with twice as many CD4 as CD8 cells. Renormalising the CD4:CD8 ratio may imply that my immune system has been ‘reset’ to resemble one a bit more like that of an HIV-negative person.

Dr Jay continues: “The key task lies in whether we can use the technique to influence viral loads. We have almost completely enrolled a 14-patient trial looking at this question.” This first study proved the gene therapy concept, and I experienced a CD4 boost, but there was never any danger of my HIV running out of control as I remained on antiretrovirals. The second study will enrol people who are not taking antiretroviral therapy to answer the bigger question of whether giving people a proportion of cells that are immune to HIV infection will reduce the available pool of cells that can be infected, reduce viral replication, and cause viral load to go down.

If you were able to manage that trick so well it drove down viral load to an undetectable level, then you might have your functional cure of HIV.

Even though my study was small, five of the six participants had an average increase of 200 CD4 cells/mm3 in one year of follow-up after the infusion. There were no adverse events in the trial. One participant did not respond to the new cells – most likely because they had a very low CD4 count to begin with, or possibly because the adenovirus vector did not ‘take’ in enough cells.

Dr Jay’s team showed that 25% of the total donated cells lacked the CCR5 co-receptor and that, after re-infusion, from 3 to 6% of those cells were present after three months.

That may not sound like a high proportion. However, the overall expansion of CD4 cells was high in all but one person and the fact that the CD4 cells reached the gut shows that they can access one of HIV’s most important ‘hiding places’. Furthermore, the hope is that, in a person not on HIV treatment, the proportion of healthy, replicating CD4 cells without CCR5 may grow in time as cells with the co-receptor are killed off by HIV.

The motivation for this approach in CCR5-deleted cells came from the successful treatment of Timothy Ray Brown, also known as the ‘Berlin patient’, which HTU covered earlier this year (see Towards a Cure for All, part 1 in issue 203). Brown, living with AIDS and leukaemia, received a bone marrow transplant from a donor with CD4 cells naturally lacking the CCR5 receptor.

Five years later, I met Brown in San Francisco. He is considered cured of HIV, and the leukaemia is in remission. His case has spawned a new wave in HIV research, including disruption of the CCR5 gene. The experiments thus far have not found the cure for HIV, but answer important questions to further the research. It’s truly an exciting time in HIV research.

I will now visit the clinic to be monitored every month for six more months, and then the study will be complete. As I look back on my treatment history I am positive that the zinc finger experiment may allow me to restore my immune system, perhaps reducing inflammation – the source of many non-AIDS-related complications like cancer and heart disease. I already see an improvement in the constant respiratory infections I used to get before I entered the study.

But best of all, I hope that one day I may be able to stop antiretroviral drugs by being infused once a year with such gene therapy techniques. Over the course of 22 years of taking meds, it’s yet another risk that appears to have paid off.

References
  1. Highleyman L Zinc finger gene therapy produces HIV-resistant CD4 T-cells. See www.aidsmap.com/page/1681138, 1 March 2011.
  2. Losso M et al. Effect of Interleukin-2 on clinical outcomes in patients with a CD4+ cell count of 300/mm3: primary results of the ESPRIT study. 16th Conference on Retroviruses and Opportunistic Infections, Montreal, abstract 90aLB, 2009.
  3. Lévy Y et al. Effect of Interleukin-2 on clinical outcomes in patients with CD4+ cell count 50 to 299/mm3: primary results of the SILCAAT study. 16th Conference on Retroviruses and Opportunistic Infections, Montreal, abstract 90bLB, 2009.
  4. Lalezari J et al. Successful and persistent engraftment of ZFN-M-R5-D autologous CD4 T Cells (SB-728-T) in aviremic HIV-infected subjects on HAART. 18th Conference on Retroviruses and Opportunistic Infections, abstract 46, Boston, 2011.