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How A Transplant "Cured" This Man Of HIV

"Even ten years later, we still have no idea how Timothy Brown was actually functionally cured."

From preexposure prophylactics to vaccines, amazing advances are being made in the fight against HIV/AIDS. But one man, Timothy Ray Brown, stands as an outlier: He's the one person effectively "cured" of HIV. The how and why of his success has been the subject of intense scrutiny for a decade.

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WASHINGTON, DC - JULY 24: Timothy Ray Brown, known as the "Berlin Patient" and the only person to have been cured of AIDS, holds a press conference to announce the launch of the Timothy Ray Brown Foundation at the Westin City Center hotel on July 24, 2012 in Washington, DC. "I wouldn't wish this on my worst enemy," Brown said of the treatment process that eventually cured him. Planned to launch during the International AIDS Conference being held in Washington, the foundation will work to focus efforts on finding a cure for HIV and AIDS.(Photo by T.J. Kirkpatrick/Getty Images)

Brown, sometimes referred to as "the Berlin patient," received a bone-marrow transplant to treat his leukemia. But doctors discovered his donor had a rare mutation that made his immune cells much harder for HIV to enter. Now, even without a daily drug regimen, Brown's viral load is undetectable.

Attempts to replicate this "miracle" have failed. (Some patients actually died shortly after receiving transplants.) To find someone with this cell mutation is rare enough, but the odds of them being a match to an HIV-positive patient—and willing to donate bone marrow—are astronomical.

"Ten years later, we still have no idea how Timothy Brown was actually functionally cured," Jonah B. Sacha, a researcher at Oregon Health & Science University, told Newsweek.

Paul Morigi/Getty Images for Kiehl's Since 1851

WASHINGTON, DC - JULY 20: AIDS survivor Timothy Ray Brown, actress Sharon Stone and Chris Salgardo, President, Kiehl's USA, pose for a photo at the 3rd Annual Kiehl's Since 1851 LifeRide For amfAR at Kiehl's Since 1851 Georgetown on July 20, 2012 in Washington, DC. (Photo by Paul Morigi/Getty Images for Kiehl's Since 1851)

Even how Brown defeated the virus is debated: Scientists initially thought the donor was immune to HIV but

further evidence suggests it was an immune response in Brown triggered by the transplant that was responsible.

Earlier this year, IrsiCaixa AIDS Research Institute in Barcelona reported that six more HIV-positive patients saw their viral loads drop to undetectable levels after receiving bone-marrow transplants. All six developed graft-versus-host disease, though, which is when donor cells start attacking the patient.

Improving transplant outcomes could lead to them as a treatment for HIV. But to do that, says Sacha, "you really need an animal model that faithfully models what happens in humans."

Rhesus monkeys have been used to test stem-cell transplantation before, but there are too many proteins in their immune systems, making the risk of rejection too high. In a new study, Sacha reported success with transplants in crab-eating macaques from Mauritius. A year after their transplants, the two recipient monkeys are alive and well—and showing no signs of rejection.

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UNSPECIFIED - MARCH 03: Crab-eating macaque, Long-tailed macaque or Cynomolgus monkey (Macaca fascicularis), Cercopithecidae. (Photo by DeAgostini/Getty Images)

Mauritius macaques all descend from five monkeys left on the island by traders 500 years ago. Just one of those macaques was female, so they have a much less diverse gene pool and are easier to match. Improving bone-marrow transplantation could open up Brown's success to others.

But Sacha, whose team published their findings last week in Nature Communications, isn't chasing a cure for HIV. He says such a thing probably doesn't exist: "Curing is just such a high bar. I think we're going to be able to put people into drug-free remission." He predicts we're about ten years away from that.

Dr. Rowena Johnston of amFAR says, ultimately, "There may be different cures for different populations of HIV-infected people."

A baby born in Mississippi in 2013 was effectively cured of HIV after being given an intense course of antiretrovirals within 30 hours of birth. The child, now a toddler, has been off antiretrovirals for a year with no signs of infection.

And in May, scientists at Temple University were able to eliminate the virus from mice transplanted with human immune cells. They edited HIV DNA out of the cells using a powerful gene editing technology known as CRISPR/Cas9.

The hope is human trials could begin as early as 2020.

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