NEWS May
09, 2019 | Original story from Howard Hughes Medical Institute
Scientists have used an
experimental therapy that relies on bacteria-infecting viruses collected, in
part, through HHMI’s SEA-PHAGES program to fight a Mycobacterium infection in a
15-year-old girl.
The patient, a 15-year-old
girl, had come to London’s Great Ormond Street Hospital for a double lung
transplant.
It was the summer of 2017, and
her lungs were struggling to reach even a third of their normal function. She
had cystic fibrosis, a genetic disease that clogs lungs with mucus and plagues
patients with persistent infections. For eight years, she had been taking
antibiotics to control two stubborn bacterial strains.
Weeks after the transplant, doctors noticed redness at the site of her surgical wound and signs of infection in her liver. Then, they saw nodules – pockets of bacteria pushing up through the skin – on her arms, legs, and buttocks. The girl’s infection had spread, and traditional antibiotics were no longer working.
Now, a new personalized treatment is helping the girl heal. The treatment relies on genetically engineering bacteriophages, viruses that can infect and kill bacteria. Over the next six months, nearly all of the girl’s skin nodules disappeared, her surgical wound began closing, and her liver function improved, scientists report May 8, 2019, in the journal Nature Medicine.
The work is the first to
demonstrate the safe and effective use of engineered bacteriophages in a human
patient, says Graham Hatfull, a Howard Hughes Medical Institute (HHMI)
Professor at the University of Pittsburgh. Such a treatment could offer a
personalized approach to countering drug-resistant bacteria. It could even
potentially be used more broadly for controlling diseases like tuberculosis.
“The idea is to use bacteriophages as antibiotics – as something we could use to kill bacteria that cause infection,” Hatfull says.
Phage hunters
In October 2017, Hatfull received the email that set his team on a months-long bacteriophage-finding quest.
A colleague at the London
hospital laid out the case: two patients, both teenagers. Both had cystic
fibrosis and had received double lung transplants to help restore lung
function. Both had been chronically infected with strains of Mycobacterium,
relatives of the bacterium that causes tuberculosis.
But maybe something else could help. Hatfull, a molecular geneticist, had spent over three decades amassing a colossal collection of bacteriophages, or phages, from the environment. Hatfull’s colleague asked whether any of these phages could target the patients’ strains.
It was a fanciful idea,
Hatfull says, and he was intrigued. His phage collection – the largest in the
world – resided in roughly 15,000 vials and filled the shelves of two
six-foot-tall freezers in his lab. They had been collected from thousands of
different locations worldwide – and largely by students.
Hatfull leads an HHMI program
called SEA-PHAGES that offers college freshmen and sophomores the opportunity
to hunt for phages. In 2018, nearly 120 universities and colleges and 4,500
students nationwide participated in the program, which has involved more than
20,000 students in the past decade.
There are more than a nonillion (that’s a quadrillion times a quadrillion) phages in the dirt, water, and air. After testing samples to find a phage, students study it. They’ll see what it looks like under an electron microscope, sequence its genome, test how well it infects and kills bacteria, and figure out where it fits on the phage family tree.
“This program engages
beginning students in real science,” says David Asai, HHMI’s senior director
for science education and director of the SEA-PHAGES program. “Whatever they
discover is new information.” That basic biological info is valuable, he says.
“Now the phage collection has actually contributed to helping a patient.”
That wasn’t the program’s original intent, Asai and Hatfull say. “I had a sense that this collection was enormously powerful for addressing all sorts of questions in biology,” Hatfull says. “But we didn’t think we’d ever get to a point of using these phages therapeutically.”
Experimental therapy
The idea of phage therapy has been around for nearly a century. But until recently, there wasn’t much data about the treatment’s safety and efficacy. In 2017, doctors in San Diego, California, successfully used phages to treat a patient with a multidrug-resistant bacterium. That case, and the rise of antibiotic resistance, has fueled interest in phages, Hatfull says.
Less than a month after he
heard about the two infected patients in London, he received samples of their
bacterial strains. His team searched their collection for phages that could
potentially target the bacteria.
They tested individual phages known to infect bacterial relatives of the patients’ strains, and mixed thousands of other phages together and tested the lot. They were looking for something that could clear the whitish film of bacteria growing on plastic dishes in the lab. If a phage could do that, the team reasoned, it might able to fight the patients’ infections.
In late January, the team
found a winner – a phage that could hit the strain that infected one of the
teenagers. But they were too late, Hatfull says. The patient had died earlier
that month. “These really are severe, life-threating infections,” he says.
His team had a few leads for
the second patient, though: three phages, named Muddy, ZoeJ, and BPs. Muddy
could infect and kill the girl’s bacteria, but ZoeJ and BPs weren’t quite so
efficient. So Hatfull and his colleagues tweaked the two phages’ genomes to
turn them into bacteria killers. They removed a gene that lets the phages
reproduce harmlessly within a bacterial cell. Without the gene, the phages
reproduce and burst from the cell, destroying it. Then they combined the trio
into a phage cocktail, purified it, and tested it for safety.
In June 2018, doctors
administered the cocktail to the patient via an IV twice daily with a billion
phage particles in every dose. After six weeks, a liver scan revealed that the
infection had essentially disappeared. Today, only one or two of the girl’s
skin nodules remain. Hatfull has high hopes: the bacteria haven’t shown any
signs of developing resistance to the phages, and his team has prepped a fourth
phage to add to the mix.
Finding the right phages for each patient is a big challenge, Hatfull says. One day, scientists may be able to concoct a phage cocktail that works more broadly to treat diseases, like the Pseudomonas infections that threaten burn patients.
“We’re sort of in uncharted
territory,” he says. But the basics of the young woman’s case are pretty
simple, he adds. “We purified the phages, we gave them to the patient, and the
patient got better.”
This article has been
republished from materials provided by Howard Hughes Medical Institute.
Note: material may have been edited for length and content. For further
information, please contact the cited source.
Reference:
Rebekah M. Dedrick et al. “Engineered bacteriophages for treatment of a patient with a disseminated drug resistant Mycobacterium abscessus.” Nature Medicine. Published online May 8, 2019. doi: 10.1038/s41591-019-0437-z
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