Back HIV/AIDS HIV/AIDS Topics HIV Treatment

New amfAR/UCSF Institute Aims to Advance Basic Science of HIV Cure Research

UCSF researchers gave an overview of their latest work at a community forum last month launching a new Institute for HIV Cure Research, funded by a $20 million grant from amfAR, the Foundation for AIDS Research, will aims to develop the scientific basis of a cure for HIV by the end of 2020. The new institute will focus on 4 key areas: learning how latent viral reservoir are formed and persist in the body, determining the precise locations of these reservoirs, quantifying the amount of virus in them, and eradicating the reservoirs from the body.

alt

"We recognize that realistically we're not talking about delivering a cure to everyone who needs it by 2020," amfAR CEO Kevin Frost said at the HIV Cure Summit on World AIDS Day (December 1). "We believe a cure is evolutionary -- we want to build the foundations and understand the science of what it takes." Frost stressed that the $20 million allocated for the first 5 years is "a floor, not a ceiling."

"The San Francisco area has a higher concentration of scientific thought leaders in HIV than anywhere else in the world," said amfAR vice president and director of research Rowena Johnston. "The Bay Area has consistently led the way in developing and implementing scientific advances in HIV prevention and treatment, and the potential for this team of researchers to develop a cure is unparalleled."

UCSF was chosen to host the institution in a national competition. It will involve collaborations with the Gladstone Institute of Virology and Immunology and Blood Systems Research Institute, the University of California at Berkeley, Oregon Health and Science University, the Infectious Disease Research Institute in Seattle, Gilead Sciences, RainDance Technologies, and Monogram Biosciences.

"San Francisco has a long and storied history of response to the HIV epidemic," said USCF Center For AIDS Research director Paul Volberding, who will also head the new institute. "This will bring together a broad team of leading scientists who believe a cure is possible, and that it will happen here. We're ready to end this epidemic."

Scientific Foundations for a Cure

Effective combination antiretroviral therapy, which debuted in the mid-1990s, has made HIV a chronic manageable disease for most people with access to treatment -- in many cases using once-daily single-tablet regimens. But the drugs are not a cure, and if they are discontinued the virus soon starts to multiply. Even during treatment, inactive HIV genetic material remains hidden in the body, and this low-level virus can cause inflammation that contributes to conditions such as cardiovascular disease and cancer.

"I don't talk to any patient who wouldn't rather be cured than take one pill once a day," Volberding said at the summit.

The past couple years have seen set-backs in the cure field, including the return of HIV in the Mississippi Baby, a child infected before birth who started antiretrovirals very early and was thought by many to be cured.

This leaves only 1 person -- Timothy Brown, known as the Berlin Patient -- who appears to have been truly cured of HIV. Brown has no detectable HIV in his blood or tissues more than 8 years after receiving bone marrow transplants from a donor with a natural mutation (CCR5-delta-32) that makes T-cells resistant to infection because they lack receptors the virus needs to enter cells.

Researchers have tried various approaches to cure HIV, including very early antiretroviral treatment, mimicking Brown's cure by protecting cells from infection, flushing the virus out of hiding and destroying it -- a strategy known as "shock and kill" -- and strengthening natural immune responses against the virus.

Many researchers now speak of a "functional cure" or remission, rather than completely eliminating HIV from the body, and most experts think a combination of approaches will be necessary.

"Let's get to a place where we don't have to take medications every day, where we don't have to experience the side effects of the medications, and where we can get our immune systems to a state where we're not at a risk of early aging," said long-time AIDS survivor and advocate Matt Sharp, speaking on a KQED program announcing the new institute. "But overall, of course, I'd like to see HIV completely eradicated from my body."

The HIV Cure Summit featured an overview by Johnston, followed by UCSF researchers who will lead the 4 teams comprising the new institute.

Warner Greene, director of the Gladstone Institute of Virology and Immunology, will head an effort to study how hidden HIV reservoirs are established and persist in the body.

"Our strategy will be to exploit the innate immune system to help flush the virus out of hiding and ultimately to eliminate its ability to bounce back when drug treatment ends," said Greene, who is investigating how molecules known as TLR agonists set off immune activation, including activation of the T-cells that harbor latent HIV.

"We need not only to shock [latent virus] but also to have a good kill strategy," he stressed. "Shock without kill is a failed strategy -- in fact it could make matters worse -- we need to make sure activated cells die. We may not be able to get every last virus, but maybe we can get to a low enough level that the immune system can control it."

Mike McCune and his team aim to figure out precisely where HIV hides within specific tissues in the body -- including how viral reservoirs differ between men and women -- while Satish Pillai's group will work on better ways to measure hidden virus that is capable of replicating.

"The population of latently infected cells is what stands between us and a cure, but our knowledge of the reservoir is still rather nebulous," said Pillai. "The Mississippi Baby showed that virus was lurking somewhere but our tools were not sensitive enough to find it. We will find more needles by sampling much more of the haystack."

Finally, Steven Deeks and his team will study how TLR agonists affect HIV reservoirs in the tissues of patients on antiretroviral treatment. So far, Gilead's experimental TLR7 agonist GS-9620 has shown "remarkable latency reversal in monkeys," he said.

"With the support of the community in San Francisco, I think we have a responsibility to take these [ideas] quickly into the clinic, to quickly identify approaches that we can safely bring into human trials," said Deeks. "We're doing this differently than the traditional academic approach, where you study something deeply and write a paper. I'm tired of that. We want to make an impact, so we're using a bit of an industry approach to move things into the clinic within next 4-5 years."

Deeks predicted that the "next big game changer" will be long-acting injectable antiretrovirals that last 1-2 months. "This will have a huge impact on people who cannot take pills on a daily basis," he said, "but it will not be a substitute for a cure."

Ultimately, Greene concluded, a cure has to be "simple, safe, effective, and scalable to the 36 million people in the world who are infected with HIV."

More Cure Research at CROI

Cure research will be among the topics of this year's Conference on Retroviruses and Opportunistic Infections, which will take place February 22-25 in Boston. The Community Cure Research Workshop on February 21, co-sponsored by the AIDS Treatment Activists Coalition, European AIDS Treatment Group, AVAC, Treatment Action Group, and Project Inform, will feature an overview for advocates of recent advances in the field and community strategy sessions to discuss how to promote cure research.

1/13/16

Sources

AmfAR. amfAR Establishes San Francisco-Based Institute for HIV Cure Research. Press release. November 30, 2015.

UCSF. $20 Million Grant from amfAR Funds Institute for HIV Cure Research. Press release. November 30, 2015.

HIV Salvage Regimens Can Safely Omit NRTIs, Study Says

Nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs) can be safely omitted from HIV salvage therapy, investigators from Brown University report in the December 15, 2015 Annals of Internal Medicine. "Omitting NRTIs will reduce pill burden, cost, and toxicity in this patient population," the study authors conclude.

alt

Read more:

6. New TAF Version of Tenofovir Approved in Combo Pill

In November the U.S. Food and Drug Administration announced the approval of Gilead Sciences' Genvoya, a new single-tablet regimen containing the integrase inhibitor elvitegravir, the booster cobicistat, emtricitabine, and tenofovir alafenamide or TAF -- a new formulation that is easier on the kidneys and bones than the older tenofovir disoproxil fumarate (TDF).

alt

Read more:

Top 10 HIV and Hepatitis Stories of 2015

Antiretroviral treatment for everyone living with HIV, expansion of pre-exposure prophylaxis (better known as PrEP) for HIV prevention, and access to interferon-free therapies for hepatitis C topped the HIV and viral hepatitis headlines this year and will continue to be major issues going into 2016. Here's a look back at some of our biggest news from 2015.

alt

Read more:

7. Simplified Dolutegravir Therapy Looks Promising

The potent HIV integrase inhibitor dolutegravir (Tivicay) taken with a single well-tolerated NRTI fully suppressed viral load in people starting antiretroviral therapy for the first time, while dolutegravir monotherapy was able to keep HIV suppressed in most treatment-experienced people who started with undetectable viral load, according to studies presented at the European AIDS Conference in October.

alt

Read more:

1. Treat Everyone Living with HIV

In September the World Health Organization released updated guidelines calling for antiretroviral therapy (ART) for everyone diagnosed with HIV regardless of CD4 T-cell count, as well as pre-exposure prophylaxis for people at substantial risk of infection. WHO estimates that the recommendations, if widely adopted, could avert 21 million deaths and prevent 28 million new infections worldwide by 2030.

alt

Read more:

8. Long-term HIV Remission and Post-Treatment Control

A young woman who was infected with HIV at birth and received very early antiretroviral therapy (ART) as a baby has maintained a viral load below the limit of detectability of standard tests for more than 12 years after stopping treatment, shedding more light on "post-treatment control" as a potential functional cure strategy.

alt

Read more: