Potential weapons against covid-19 include manufactured antibodies, serum transfusions from survivors, antivirals, steroids, and more than 100 vaccine candidates, some now advancing toward decisive tests in volunteers.
But there’s another approach to battling the virus—one that hasn’t won much attention, but which in the future could become the fastest way to beat back a pandemic. It involves isolating genetic material from survivors and injecting it directly into others, lending them protection against the pathogen.
DNA-encoded antibodies, as these therapeutics are called, have shown promising results in animals. In humans, genes injected into the arm or leg would convert the recipient’s muscle cells into factories to make antibodies against the virus. That could provide temporary immunity or lessen the severity of the disease for those already infected.
While no DNA-encoded antibody against covid-19 has yet reached human tests, laboratory experiments have started, says David Weiner, director of the vaccine and immunotherapy center at the Wistar Institute, who says his center has tested anti-covid gene injections on animals.
The use of conventional antibody drugs is one of the most promising treatment options for covid-19. Those drugs, however, must be produced in specialized bio-manufacturing facilities, which could limit their availability.
In contrast, gene therapy could offer a way to skip the complex and costly manufacturing of delicate antibodies and avoid the uncertainties involved in vaccines. As well, scientists say, gene injections can be used to carry information for more than one antibody at a time, which could stop a virus from developing resistance.
The advantage of the technique, researchers say, is its speed and low cost. DNA is manufactured in bacteria, which double in number every 30 minutes. “You can make DNA very readily, it’s dirt cheap, and you let the muscle make the antibody,” says Henry Ji, CEO of Sorrento, who says his company is exploring the idea with a partner, SmartPharm, of Boston.
Already in the works
Before the covid-19 pandemic, several universities and biotech companies were given tens of millions by DARPA, the US Defense Department’s science agency, to test the concept under a program to generate treatments against never-seen-before infections in 60 days.
In technology “sprints” organized by DARPA last year, teams at Wistar, Vanderbilt University, and the biotech firm AbCellera, among others, were asked to show whether they could develop an antidote to a known virus, such as Zika or pandemic H1N1 influenza, in two months. Each started with only with a blood sample from a survivor.
The process involved identifying an antibody to the pathogen in the survivor’s blood serum, isolating the genetic instructions to make it, and then injecting the DNA (or RNA) into mice. “We basically had a stopwatch to see how fast they could do the whole process,” says Amy Jenkins, who manages the program at DARAP.
At Vanderbilt, researchers live-tweeted their sprint to develop an anti-Zika shot. AbCellera, based in Vancouver, says that mice given a gene shot were able to survive a super-dose of avian influenza, 20 times the fatal amount. In both cases, antibodies made by muscle cells appear to have successfully stopped the infection.
DARPA had plans for a harder challenge in 2022, in which the teams would respond to a surprise virus chosen by the agency. But then the pandemic hit. “We didn’t have to give them a pathogen,” says Jenkins. “It found us, and it found us two years early.”
Spreading out your bets
In the rush that followed, DARPA’s planning proved useful, says Robert Carnahan, associate director of Vanderbilt’s vaccine center, since the groups were prepared to quickly locate convalescent antibodies from the blood of covid-19 survivors. Vanderbilt did so and sold the discovery to the pharmaceutical company AstraZeneca this April. In June, drug maker Eli Lilly said it would start testing antibodies found by AbCellera in covid-19 patients.
Go to Publisher: MIT Technology Review
Author: Antonio Regalado