Almost three years after an HIV-positive man in Britain received bone marrow stem cells from a donor with a rare genetic mutation that resists HIV infection, doctors say he has become the second known adult worldwide to be cleared of the AIDS virus.
Doctors added that the man underwent highly sensitive tests that are still showing no trace of a previous HIV infection.
“There is no virus there that we can measure. We can’t detect anything,” said Ravindra Gupta, a professor and HIV biologist who co-led a team of doctors treating the man.
AIDS experts said the case is a proof of the concept that scientists will one day be able to end AIDS, and marks a “critical moment” in the search for an HIV cure, but does not mean that cure has already been found.
Gupta described his patient as “functionally cured” and “in remission,” but cautioned: “It’s too early to say he’s cured.”
The man is being called “the London patient,” in part because his case is similar to the first known case of a functional cure of HIV — in an American man, Timothy Brown, who became known as the Berlin patient when he underwent similar treatment in Germany in 2007 which also cleared his HIV.
Brown, who had been living in Berlin, has since moved to the United States and, according to HIV experts, is still HIV-free.
Some 37 million people worldwide are currently infected with HIV and the AIDS pandemic has killed about 35 million people worldwide since it began in the 1980s. Scientific research into the complex virus has in recent years led to the development of drug combinations that can keep it at bay in most patients.
Gupta, now at Cambridge University, treated the London patient when he was working at University College London. The man had contracted HIV in 2003, Gupta said, and in 2012 was also diagnosed with a type of blood cancer called Hodgkin’s Lymphoma.
In 2016, when he was very sick with cancer, doctors decided to seek a transplant match for him.
“This was really his last chance of survival,” Gupta told Reuters.
The donor — who was unrelated — had a genetic mutation known as CCR5 delta 32, which confers resistance to HIV.
The transplant went relatively smoothly, Gupta said, but there were some side effects, including the patient suffering a period of “graft-versus-host” disease — a condition in which donor immune cells attack the recipient’s immune cells.
Most experts say it is inconceivable such treatments could be a way of curing all patients. The procedure is expensive, complex and risky. To do this in others, exact match donors would have to be found in the tiny proportion of people and most of them of northern European descent, who have the CCR5 mutation that makes them resistant to the virus.
“Although this is not a viable large-scale strategy for a cure, it does represent a critical moment,” said Anton Pozniak, president of the International AIDS Society. “The hope is that this will eventually lead to a safe, cost-effective and easy strategy … using gene technology or antibody techniques.”
Specialists said it is also not yet clear whether the CCR5 resistance is the only key — or whether the graft-versus-host disease may have been just as important. Both the Berlin and London patients had this complication, which may have played a role in the loss of HIV-infected cells, Gupta said.
His team plans to use these findings to explore potential new HIV treatment strategies. “We need to understand if we could knock out this (CCR5) receptor in people with HIV, which may be possible with gene therapy,” he said.
The London patient, whose case was set to be reported in the journal Nature and presented at a medical conference in Seattle on Tuesday, has asked his medical team not to reveal his name, age, nationality or other details.
By Kate Kelland/Reuters
Reporting by Kate Kelland; editing by Catherine Evans.
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